My friend and I was shopping around when I found this bargain.
D&G watches -- 70% of the selling price in HKD
Burberry -- 80%
Tissot -- 75%
other brands -- 65%
Ooops!!! I got a D&G watch! (post its picture to you later)
The shop is located in Causeway Bay, I don't remember the exact location but it is near the MTR station.
Haha~if anyone wants to buy watches! You can PM me or leave comment for the information~ I could go there to get one for you.
Time to work~
Saturday, 16 April 2011
Friday, 15 April 2011
An Ode to a Love
The sun is sinking
my Eyes are sobbing
- as it cries my parting to you...
.
The Sun is missing
my heart is breaking
- as it beats my longing to you...
Soon, the sun is rising
my lips be uttering
- the special LOVE i'll cherish on you.
http://wwwthelonelyplanet.blogspot.com/?expref=next-blog
my Eyes are sobbing
- as it cries my parting to you...
.
The Sun is missing
my heart is breaking
- as it beats my longing to you...
Soon, the sun is rising
my lips be uttering
- the special LOVE i'll cherish on you.
http://wwwthelonelyplanet.blogspot.com/?expref=next-blog
Primary cell cultures
The cell types used in cell culture fall into two categories generally referred to as either a primary cultured or a cell line.
Primary cell cultures
Primary cultures are cells derived directly from tissues following enzymatic dissociation or from tissue fragments referred to as explain. These are usually the cells of preference, since it is argued that primary cultures retain their characteristics and reflect the true activity of the cell type in vivo. The disadvantage in using primary culture, is that isolation can be labor intensive and may produce a heterogeneous population of cells. Moreover primary cultures have a relatively limited life span and can be used over only a limited period of time in culture.
Primary cultures can be obtained from many different tissues and the source from the endothelium of blood vessels are referred to as endothelial cells whilst those isolated from teh medial layer of the blood vessels and other similar tissues are smooth muscle cells. Although both can be obtained from the same vessels, endothelial cells are different in morphology and function, generally growing as a single monolayer characterised by a cobble-stoned morphology. Smooth muscle cells on the other hand are elongated, with spindle-like projections at either end and grow in layers even when maintained in culture. In addition to these cell types there are several other widely used primary cultures derived from a diverse range of tissues, including fibroblasts from connective tissue, lymphocytes from blood, neurones from nervous tissues and hepatocytes from liver tissue.
Primary cell cultures
Primary cultures are cells derived directly from tissues following enzymatic dissociation or from tissue fragments referred to as explain. These are usually the cells of preference, since it is argued that primary cultures retain their characteristics and reflect the true activity of the cell type in vivo. The disadvantage in using primary culture, is that isolation can be labor intensive and may produce a heterogeneous population of cells. Moreover primary cultures have a relatively limited life span and can be used over only a limited period of time in culture.
Primary cultures can be obtained from many different tissues and the source from the endothelium of blood vessels are referred to as endothelial cells whilst those isolated from teh medial layer of the blood vessels and other similar tissues are smooth muscle cells. Although both can be obtained from the same vessels, endothelial cells are different in morphology and function, generally growing as a single monolayer characterised by a cobble-stoned morphology. Smooth muscle cells on the other hand are elongated, with spindle-like projections at either end and grow in layers even when maintained in culture. In addition to these cell types there are several other widely used primary cultures derived from a diverse range of tissues, including fibroblasts from connective tissue, lymphocytes from blood, neurones from nervous tissues and hepatocytes from liver tissue.
Prey I Hunted -- 80% selling price Watches I could get~
Today, I have shopping around and meet my friends~ Some of them are working in Watches Shop. They have got some employee discount.--20% off
I have seen the watches below they give to me and choose DW0267 with price HKD$1320.
Here is the bargain I've found today. ~ I'm lucky to have these friends^^
Separation Examples -- Insights Into the "minds" of chromatographers
Amino Acids (Column, ionic modifier)
a) Underivatised amino acids (C8, citrate -SDS)
b) underivatised amino acids (amine, phosphate)
c) iodoamino acids (c8, acetic acid)
d) 3-methylhistidine (c18, C6SO3Na)
e,f) PTH-amino acids (C18, ammonium acetate)
g,h) dansyl-amino acids (C18, phosphate)
i) dansylated protein hydrolysate (C18, phosphate)
j) dinitrophenyl-amio acids derivative (silica, isoctane-iPrOH-CH2Cl2)
k) Dansyl-amino acids (C8, C12-dien-Zn(II))
l) dansyl-amino acid enantiomers (C8, L-2-isopropyl-dien-Zn(II))
m) resolution of D, L-Valine (C18, Cu (L-Pro)2)
n, o) fluorescent O-phthalaldehyde-amino acid derivatives (C18, phosphate)
The effective separation of amino acids and their derivatives has been readily achieved by reversed phase HPLC. The examples A to O in this section show a representative selection of separations of these solutes. In addition, the following sections of teh text give useful information.
Separation of free amino acids.
The polar amino acids are insufficiently retained on non-polar, reversed phase columns for adequate resolution. Example A shows that the use of a mobile phase which contains sodium dodecylsulphate (SDS) allows adequate retention and thus separation of these solute. Alternatively a polar column (Example B) can be used to achieve this separation.
Example C shows that a buffered aqueous mobile phase is adequate to achieve the separation of the relatively hydrophobic, iodeamino acids. Similarly reversed phase HPLC has been particularly successful in the separation of tryphtophan and other aromatic amino acids from a variety of extracts. A recent example is the analysis of tryphtophan and phenylalanine metabolites in urine by M. Ghebregzabher, et al. Alternatively HPLC techniques can be used to monitor enzymatic activities, such as tryptophan 5-mono-oxygenase activity in brain preparations.
The analysis of polar amino acids in the complex mixtures present in tissue preparations can be achieved with the use of hydrophobic ion pairing reagents. Example D shows a typical separation that was achieved with an alkysulphonate and allowed the analysis of 3-methylhistidine in urine. Baker et al used hexane sulphonate in the analysis of guanidino compounds such as arginine and taurocyamine.
a) Underivatised amino acids (C8, citrate -SDS)
b) underivatised amino acids (amine, phosphate)
c) iodoamino acids (c8, acetic acid)
d) 3-methylhistidine (c18, C6SO3Na)
e,f) PTH-amino acids (C18, ammonium acetate)
g,h) dansyl-amino acids (C18, phosphate)
i) dansylated protein hydrolysate (C18, phosphate)
j) dinitrophenyl-amio acids derivative (silica, isoctane-iPrOH-CH2Cl2)
k) Dansyl-amino acids (C8, C12-dien-Zn(II))
l) dansyl-amino acid enantiomers (C8, L-2-isopropyl-dien-Zn(II))
m) resolution of D, L-Valine (C18, Cu (L-Pro)2)
n, o) fluorescent O-phthalaldehyde-amino acid derivatives (C18, phosphate)
The effective separation of amino acids and their derivatives has been readily achieved by reversed phase HPLC. The examples A to O in this section show a representative selection of separations of these solutes. In addition, the following sections of teh text give useful information.
Separation of free amino acids.
The polar amino acids are insufficiently retained on non-polar, reversed phase columns for adequate resolution. Example A shows that the use of a mobile phase which contains sodium dodecylsulphate (SDS) allows adequate retention and thus separation of these solute. Alternatively a polar column (Example B) can be used to achieve this separation.
Example C shows that a buffered aqueous mobile phase is adequate to achieve the separation of the relatively hydrophobic, iodeamino acids. Similarly reversed phase HPLC has been particularly successful in the separation of tryphtophan and other aromatic amino acids from a variety of extracts. A recent example is the analysis of tryphtophan and phenylalanine metabolites in urine by M. Ghebregzabher, et al. Alternatively HPLC techniques can be used to monitor enzymatic activities, such as tryptophan 5-mono-oxygenase activity in brain preparations.
The analysis of polar amino acids in the complex mixtures present in tissue preparations can be achieved with the use of hydrophobic ion pairing reagents. Example D shows a typical separation that was achieved with an alkysulphonate and allowed the analysis of 3-methylhistidine in urine. Baker et al used hexane sulphonate in the analysis of guanidino compounds such as arginine and taurocyamine.
Equipment design
Most commercial systems can be purchased in a form which includes gradient elution capabilitie, a variable vavelength detecter capable of wavelengths down to 200 nm, and/or a refractive index detector and a low dead-volume injector.
There are a large number of liquid chromatographs available and the choice can be rather bewildering. Almost all current manufacturers produce a reliable instrument and an individual's choice is often determined by factors such as good local service from a particular firm and the amount of money available to purchase the instrument. The researcher should also carefully consider teh experimental requirements of the separations that are to be achieved; for example, a 254nm UV detector is of little use for monitoring the separation of pepetides and proteins which are best detected at 206-226 nm, or a saturated lipid, which does not exhibit significant absorption above 195 nm, will require another form of detection, e.g. refractive index.
Most modern systems are based on a constant volume reciprocating pump which can generate pressures of up to 6000 psi, which is a practical upper limit as many columns do not have a satisfactory life-time much above 5000 psi. On the other hand, the use of the viscous eluants such as propanol can require pressures of 3000 psi. Pulse free pumps are neccessary as pulsations within the system can result in a noisy detector baseline and thus raise the detection limits in sensitive assays. Multi-head reciprocating pumps have been designed to operate in an asymmetric manner and thus compensate for variations in flow rates during the strokes of piston. Such a system when used with small volume pistons allows the rapid generation of almost pulse free gradients which is an important feature for the analysis of biological samples. It is essential that the pump(s) maintain constant operating conditions so that retention times in consecutive replicate assays should agree by 0.5%.
A major difference between many commercial systems is the use of one or two pumps for the generation of a solvent gradient. The gradient can be formed on either the low or high pressure side of the pump system. Either system can be used to generate reliable gradients provided small-volume piston pumps are used and teh mixing vessel has a minimal total volume (0.6 mL or less) which allows rapid and complete mixing of the solvents. A new advance in pump design has occurred with teh development of microprocessor controls which allow the use of a single multi-headed pump for the generation of complex gradient shapes.
An alternative to teh continuous gradient is the stepwise change of the mobile phase by means of a solvent select value. If there is a sufficiently large number of solvent changes, the " stepwise gradient" approaches the true gradient. Since this system requires only the pump it is less expensive and with an optimal set-up the performance of this system can approach that of a true gradient apparatus.
Other options which individual separations can require are temperature control, flow programming, complex gradient generation, variable wavelength UV detection, UV scanning of peaks during a run, fraction collecting, recycle mode, higher flow rates for preparative columns, fluorescent detection, automatic injecion and sampling, and intergration facilities. A major advantage of microprocessor controlled facilities is that the instrument can be programmed to execute a multi-step gradient analysis and then re-equilibrate the column for the next analysis. On the more expensive instruments, the control system can allow unattended methods development with repeated injections under different chromatographic conditions, thus allowing rapid development of the optimum separation conditions. Since the analysis of a biological sample depends on teh complex interaction of a number of variables, a microprocessor control system is not an expensive luxury but rather an important part of the modern liquid chromatograph.
There are a large number of liquid chromatographs available and the choice can be rather bewildering. Almost all current manufacturers produce a reliable instrument and an individual's choice is often determined by factors such as good local service from a particular firm and the amount of money available to purchase the instrument. The researcher should also carefully consider teh experimental requirements of the separations that are to be achieved; for example, a 254nm UV detector is of little use for monitoring the separation of pepetides and proteins which are best detected at 206-226 nm, or a saturated lipid, which does not exhibit significant absorption above 195 nm, will require another form of detection, e.g. refractive index.
Most modern systems are based on a constant volume reciprocating pump which can generate pressures of up to 6000 psi, which is a practical upper limit as many columns do not have a satisfactory life-time much above 5000 psi. On the other hand, the use of the viscous eluants such as propanol can require pressures of 3000 psi. Pulse free pumps are neccessary as pulsations within the system can result in a noisy detector baseline and thus raise the detection limits in sensitive assays. Multi-head reciprocating pumps have been designed to operate in an asymmetric manner and thus compensate for variations in flow rates during the strokes of piston. Such a system when used with small volume pistons allows the rapid generation of almost pulse free gradients which is an important feature for the analysis of biological samples. It is essential that the pump(s) maintain constant operating conditions so that retention times in consecutive replicate assays should agree by 0.5%.
A major difference between many commercial systems is the use of one or two pumps for the generation of a solvent gradient. The gradient can be formed on either the low or high pressure side of the pump system. Either system can be used to generate reliable gradients provided small-volume piston pumps are used and teh mixing vessel has a minimal total volume (0.6 mL or less) which allows rapid and complete mixing of the solvents. A new advance in pump design has occurred with teh development of microprocessor controls which allow the use of a single multi-headed pump for the generation of complex gradient shapes.
An alternative to teh continuous gradient is the stepwise change of the mobile phase by means of a solvent select value. If there is a sufficiently large number of solvent changes, the " stepwise gradient" approaches the true gradient. Since this system requires only the pump it is less expensive and with an optimal set-up the performance of this system can approach that of a true gradient apparatus.
Other options which individual separations can require are temperature control, flow programming, complex gradient generation, variable wavelength UV detection, UV scanning of peaks during a run, fraction collecting, recycle mode, higher flow rates for preparative columns, fluorescent detection, automatic injecion and sampling, and intergration facilities. A major advantage of microprocessor controlled facilities is that the instrument can be programmed to execute a multi-step gradient analysis and then re-equilibrate the column for the next analysis. On the more expensive instruments, the control system can allow unattended methods development with repeated injections under different chromatographic conditions, thus allowing rapid development of the optimum separation conditions. Since the analysis of a biological sample depends on teh complex interaction of a number of variables, a microprocessor control system is not an expensive luxury but rather an important part of the modern liquid chromatograph.
General texts
Several excellent general texts have been published on liquid chromatography and the reader is referred to the list at the end of the chapter for an introduction to the technique. Past developments have concentrated heavily on pharmaceutical applications, but the general concepts and techniques are quite applicable to teh analysis of biological materials.
What is HPLC?
What is HPLC?
HPLC is best decribed as high performance liquid chromatography since the essence of the technique is the highly resolutive separations which can be achieved by teh use of uniform microparticulate chromatographic supports and well designed equipment. Other acronyms such as high pressure or high speed liquid chromatography are often used but do not reflect the essential features of the technique.
The use of liquid chromatography for the analysis of biological materials has many advantages over teh classical technique of gas chromatography, since the liquid mobile phase allows the separation and recovery of substances which are not readily volatilized. In addition, liquid chromatography is to be preferred for molecules which have high polarity, high molecular weight, a number of ionic groups or thermal instability. Such as features are characteristic of most biological macromolecules, and have caused many difficulties in other chromatographic studies.
The use of a liquid instead of a gaseous phase introduces several important constraints on the chromatographic system. Since liquids are more viscous (20 to 200 times) and exhibit lower diffusion rates (3,000 to 30, 000 times) than gases, the separation columns must be operated at higher pressures in high performance liquid chromatography (500 -5000 psi) than in gas chromatography. The analysis time is kept short in liquid chromatography by the use of small columns (typically 4 mm by 30 cm) and small particle sizes (<10u). Recently analysis times have been further improved by the introduction of 5-6u particles. HPLC columns are usually 25 to 50 cm long and have internal diamters from 2 to 4 mm with linear flow velocities of teh mobile phase of typically 20 cm/min; conventional columns are much larger and have usual elution velocities of 0.1 cm/min. Another advantage in HPLC is that closed, reusable columns are used, thus hundreds of samples can be run through an individual coumn without repacking.
Biological macromolecules are usually structurally complex. For example, nucleic acids often exhibit molecular weights in excess of 1x10^6, while proteins, although smaller, exhibit great diversity due to teh occurrence of twenty different amino acids in protein sequences. Polysaccharides often contain an enormous number of branch points in the carbohydrate backbone and therefore can present a tremendous separation challenge. In many classes of lipid the nature of any esterified fatty acid is highly heterogeneous, with saturated and unsaturated acids of different chain lengths present in many purified lipid preparations.
It is clear, therefore, that the selectivity available with microparticulate silica-based columns will be fully utilized in biological analysis. Already several published seaprations suggest that the resolving power of this new chromatographic technique is excellent, eg. porcine insulin is well separated from the monodesamido derivative (charge difference of -1), ovine and porcine endorphins (difference of a single methyl group) can be completely resolved.
HPLC is best decribed as high performance liquid chromatography since the essence of the technique is the highly resolutive separations which can be achieved by teh use of uniform microparticulate chromatographic supports and well designed equipment. Other acronyms such as high pressure or high speed liquid chromatography are often used but do not reflect the essential features of the technique.
The use of liquid chromatography for the analysis of biological materials has many advantages over teh classical technique of gas chromatography, since the liquid mobile phase allows the separation and recovery of substances which are not readily volatilized. In addition, liquid chromatography is to be preferred for molecules which have high polarity, high molecular weight, a number of ionic groups or thermal instability. Such as features are characteristic of most biological macromolecules, and have caused many difficulties in other chromatographic studies.
The use of a liquid instead of a gaseous phase introduces several important constraints on the chromatographic system. Since liquids are more viscous (20 to 200 times) and exhibit lower diffusion rates (3,000 to 30, 000 times) than gases, the separation columns must be operated at higher pressures in high performance liquid chromatography (500 -5000 psi) than in gas chromatography. The analysis time is kept short in liquid chromatography by the use of small columns (typically 4 mm by 30 cm) and small particle sizes (<10u). Recently analysis times have been further improved by the introduction of 5-6u particles. HPLC columns are usually 25 to 50 cm long and have internal diamters from 2 to 4 mm with linear flow velocities of teh mobile phase of typically 20 cm/min; conventional columns are much larger and have usual elution velocities of 0.1 cm/min. Another advantage in HPLC is that closed, reusable columns are used, thus hundreds of samples can be run through an individual coumn without repacking.
Biological macromolecules are usually structurally complex. For example, nucleic acids often exhibit molecular weights in excess of 1x10^6, while proteins, although smaller, exhibit great diversity due to teh occurrence of twenty different amino acids in protein sequences. Polysaccharides often contain an enormous number of branch points in the carbohydrate backbone and therefore can present a tremendous separation challenge. In many classes of lipid the nature of any esterified fatty acid is highly heterogeneous, with saturated and unsaturated acids of different chain lengths present in many purified lipid preparations.
It is clear, therefore, that the selectivity available with microparticulate silica-based columns will be fully utilized in biological analysis. Already several published seaprations suggest that the resolving power of this new chromatographic technique is excellent, eg. porcine insulin is well separated from the monodesamido derivative (charge difference of -1), ovine and porcine endorphins (difference of a single methyl group) can be completely resolved.
Wednesday, 13 April 2011
Pavlova 雜莓
材料: for 4-6
蛋白 3 隻
砂糖 120 克
白酒醋 1 茶匙
粟粉 1 茶匙
覆盆子果茸 2 湯匙
藍莓 1 盒
士多啤梨 6粒
做法
1. 打發蛋白至企身, 砂糖分兩次加入拂打擊
2. 放糖、醋及粟粉
3. 將打好的蛋白霜搯到鋪上牛油紙的焗盤上，造成直徑10cm的圓形
4. 用匙羹輕輕壓出小凹位
5. 150度焗1小時
6. 放上藍莓及一開四之士多啤梨，最後淋上覆盆子果茸
蛋白 3 隻
砂糖 120 克
白酒醋 1 茶匙
粟粉 1 茶匙
覆盆子果茸 2 湯匙
藍莓 1 盒
士多啤梨 6粒
做法
1. 打發蛋白至企身, 砂糖分兩次加入拂打擊
2. 放糖、醋及粟粉
3. 將打好的蛋白霜搯到鋪上牛油紙的焗盤上，造成直徑10cm的圓形
4. 用匙羹輕輕壓出小凹位
5. 150度焗1小時
6. 放上藍莓及一開四之士多啤梨，最後淋上覆盆子果茸
Tres Leche cake
Tres Leche cake
Tres Leche Cake was served at the Historymakers Gala at Camelback Inn on February 11. It was an historic evening with an awesome menu. Of course, I loved the desserts. This was one of them. Found this recipe on allrecipe.com. Another dessert that is so delicious is Summer Trifle on page 154 of Tastes & Treasures.We also premiered the new Centennial book ARIZONA Recollections and Reflections that night. Wonderful history of Arizona and it's Historymakers.
Ingredients
* 3/4 cup butter, softened
* 1 1/2 cups white sugar
* 9 egg yolks
* 1 teaspoon vanilla extract
* 2 cups all-purpose flour
* 1 1/2 teaspoons baking powder
* 1 cup milk
* 9 egg whites
* 1 teaspoon cream of tartar
* 2 cups heavy whipping cream
* 1 (5 ounce) can evaporated milk
* 1 (14 ounce) can sweetened condensed milk
* 2 cups heavy whipping cream
* 1 cup white sugar
Directions
1. Preheat oven to 350 degrees F (175 degrees C). Grease and flour a 9x13 inch pan.
2. In a large bowl, cream together the butter and sugar until light and fluffy. Add the egg yolks one at a time, beating well with each addition, then stir in the vanilla. Sift together the flour and baking powder. Add the flour mixture alternately with the milk; beat well after each addition. In a large glass or metal mixing bowl, beat egg whites and cream of tartar until whites form stiff peaks. Gently fold the egg whites into the cake batter using a rubber spatula. Spread the mixture evenly into the prepared pan.
3. Bake in the preheated oven for 25 to 30 minutes, or until a toothpick inserted into the cake comes out clean. Allow to cool.
4. In a small bowl, stir together the 2 cups heavy cream, evaporated milk and sweetened condensed milk. Pour the mixture over the cake until it wont absorb any more. You may have 1/3 to 1/4 left over. That's okay.
5. Combine the whipped cream and sugar, spread over soaked cake. Refrigerate cake until serving, Pour leftover milk mixture onto plates and swirl in jam if desired, before setting cake on the plates.
Nutritional Information open nutritional information
Amount Per Serving Calories: 365 | Total Fat: 20.7g | Cholesterol: 141mg
Monday, 11 April 2011
FT Island After Love
FT Island --After Love 사랑후애
<---A good song I recently listen to^^---->
<--- If you are learning korean like me, recommend you to listen la-->
English lyrics:
<---A good song I recently listen to^^---->
<--- If you are learning korean like me, recommend you to listen la-->
English lyrics:
Lyrics:
I thought you were my love, my life, and
You held my whole world in your hands
How could I let you say:" good bye", I believed you were the one
My soul could only smile with you
My heart can only beat with you
To me you was true happiness
Like a fool, I believed in your love
And, it was all a lie
Oh, it was all a lie
Your love-with-me-completely was totally a lie
This love has cut me deep inside,
caused chaos in my mind
Leaving me with nothing but to cry
You said that you'd never go
Did you protect me? No
Your love-with-me-completely was totally a lie
Because you've taken all of my heart
Love's tearing me apart
Suddenly, you're telling me: "good bye"
A dream: receiving your lover's true heart
And giving mine, Saying you'll never be apart
Like a fool, I let you have it all
I believed that you were mine
And, it was all a lie
Oh, it was all a lie
Your love with-me-completely was totally a lie
This love has cut me deep inside
caused chaos in my mind
Leaving me with nothing but to cry
You said that you'd never go
Did you protect me? No
Your love with-me-completely was totally a lie
Because you've taken all of my heart
Love's tearing me apart
Suddenly, you're telling me:" good bye"
What my hearts felt was a lie
The words you spoke were also a lie
When you told me it will be forever, you lied
It was a heartless crime to leave me here with hope
Where did you go?
Where did you go? Far away...
I need to tell you I love you
Won't you Please come back to me
I'm begging, don't you see
Without you, To love I say to it : "good bye"
Though it's cut me deep inside
Caused chaos in my mind
I'm waiting, just to look into your eyes
Because It was all a lie
Oh This is all a lie
Your love with-me-completely was totally a lie
Because you're my only one
When will world return?
Will I wait until the Day I die?
I thought you were my love, my life, and
You held my whole world in your hands
How could I let you say:" good bye", I believed you were the one
My soul could only smile with you
My heart can only beat with you
To me you was true happiness
Like a fool, I believed in your love
And, it was all a lie
Oh, it was all a lie
Your love-with-me-completely was totally a lie
This love has cut me deep inside,
caused chaos in my mind
Leaving me with nothing but to cry
You said that you'd never go
Did you protect me? No
Your love-with-me-completely was totally a lie
Because you've taken all of my heart
Love's tearing me apart
Suddenly, you're telling me: "good bye"
A dream: receiving your lover's true heart
And giving mine, Saying you'll never be apart
Like a fool, I let you have it all
I believed that you were mine
And, it was all a lie
Oh, it was all a lie
Your love with-me-completely was totally a lie
This love has cut me deep inside
caused chaos in my mind
Leaving me with nothing but to cry
You said that you'd never go
Did you protect me? No
Your love with-me-completely was totally a lie
Because you've taken all of my heart
Love's tearing me apart
Suddenly, you're telling me:" good bye"
What my hearts felt was a lie
The words you spoke were also a lie
When you told me it will be forever, you lied
It was a heartless crime to leave me here with hope
Where did you go?
Where did you go? Far away...
I need to tell you I love you
Won't you Please come back to me
I'm begging, don't you see
Without you, To love I say to it : "good bye"
Though it's cut me deep inside
Caused chaos in my mind
I'm waiting, just to look into your eyes
Because It was all a lie
Oh This is all a lie
Your love with-me-completely was totally a lie
Because you're my only one
When will world return?
Will I wait until the Day I die?
Hagual lyrics
Nae sarangiira saengakhaetgo
Nae juhnboorago saengakhaetgo
Nae majimakii dwil sarang geugeh nuhrago miduhsuh
Nuh hanamaneul wihae ootgo
Nuh hanamaneul wihae sargo
Geueh haengbok irgguhrago ni sarangeul midutneundeh
Modu da guhjitmariya da guhjitmariya
Nuh-eh sarangeun da guhjitmariya
Itorok apeugeh haesuh
Nar seurpeugeh haesuh oolligo gan sarangijanah
Namaneul saranghandago nal jikyuhjoondago
Nuh-eh sarangeun da gujitmariya
Nae maeum da gajyuhgago sarangdo gajyuhgagoh
Ddunaneun geh sarang ii janah
Han saramehgeh sarang badgo
Han saramehgeh sarangjoogo
Geu saramii nuhilgguhra babochuhruhm midutneundeh
Namaneul saranghandago nal jikyuhjoondago
Nuh-eh sarangeun da gujitmariya
Nae maeum da gajyuhgago sarangdo gajyuhgagoh
Ddunaneun geh sarang ii janah
Sarangiirahneun mareun guhjitmal
Sarangeul handan mardoh guhjitmal
Youngwoniiraneun mardoh guhjitmal
Doraondaneun yaksokmaneul naegeh namgin chae
Geudaeneun uhdiroh (jakkuman muruhjanah)
Geudaeneun uhdiroh murhuhjigoh muruhjyuhdoh
Naneun nuh hanamaneul saranghae
Nuh dashi doraorkabwa naegehroh orkabwa
Naneun sarangeul dashi mot-hajana
Itorok apeuge haedoh nal seurpeugehhaedoh
Nuh hanaman gidarijana
Modu da guhjitmariya da guhjitmariya
Oori ibyureun da guhjitmariiya
Niga nae sarang iinika nae junbooiinikka
Nuh hanaman gidarijana
Nae juhnboorago saengakhaetgo
Nae majimakii dwil sarang geugeh nuhrago miduhsuh
Nuh hanamaneul wihae ootgo
Nuh hanamaneul wihae sargo
Geueh haengbok irgguhrago ni sarangeul midutneundeh
Modu da guhjitmariya da guhjitmariya
Nuh-eh sarangeun da guhjitmariya
Itorok apeugeh haesuh
Nar seurpeugeh haesuh oolligo gan sarangijanah
Namaneul saranghandago nal jikyuhjoondago
Nuh-eh sarangeun da gujitmariya
Nae maeum da gajyuhgago sarangdo gajyuhgagoh
Ddunaneun geh sarang ii janah
Han saramehgeh sarang badgo
Han saramehgeh sarangjoogo
Geu saramii nuhilgguhra babochuhruhm midutneundeh
Namaneul saranghandago nal jikyuhjoondago
Nuh-eh sarangeun da gujitmariya
Nae maeum da gajyuhgago sarangdo gajyuhgagoh
Ddunaneun geh sarang ii janah
Sarangiirahneun mareun guhjitmal
Sarangeul handan mardoh guhjitmal
Youngwoniiraneun mardoh guhjitmal
Doraondaneun yaksokmaneul naegeh namgin chae
Geudaeneun uhdiroh (jakkuman muruhjanah)
Geudaeneun uhdiroh murhuhjigoh muruhjyuhdoh
Naneun nuh hanamaneul saranghae
Nuh dashi doraorkabwa naegehroh orkabwa
Naneun sarangeul dashi mot-hajana
Itorok apeuge haedoh nal seurpeugehhaedoh
Nuh hanaman gidarijana
Modu da guhjitmariya da guhjitmariya
Oori ibyureun da guhjitmariiya
Niga nae sarang iinika nae junbooiinikka
Nuh hanaman gidarijana
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