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Absorbance (A), also known as optical density (OD), is the quantity of light absorbed by a solution. Transmittance is the quantity of light that passes through a solution[1]. Absorbance and % transmittance are often used in spectrophotometry and can be expressed by the following:
Absorbance equation
- A = Log10 (I0/I)
where I0 is the intensity of the incident light, and I is intensity of that light after it passed through the sample
- T = I/I0 and %T = 100 (T)
The equation that allows one to calculate absorbance from % transmittance is
- A = 2 - Log10 (%T)
Determine concentration using the Beer-Lambert Law
The concentration of a sample can be calculated from its absorbance using the Beer–Lambert law, which is expressed as follows:
- A = ε * c * p
Where ε is the molar absorptivity, or molar extinction coefficient, in L* mol-1 *cm-1;
c is the concentration of the solute in solution, in mol/L;
p is the path length of the sample, in cm, for example 1 cm for a cuvette.
ε260[2]
Would you believe that the extinction coefficient for a sequence as short as 6 bases can vary just by arranging the bases in a different order? Additionally, base composition can lead to significant differences in the extinction coefficient.
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OD260
The amount of oligonucleotide in nanomoles that, when dissolved in 1 mL volume, results in 1 unit of absorbance at 260 nm with a standard 1 cm path-length cuvette. nmole/OD260 is calculated from oligonucleotide's molar extinction coefficient. OD260 is calculated from the following equation,
- OD260 = (A260 * V) / p
where A260 is the absorbance at 260 nm, V is the solution volume in mL, and p is the length of the light path through the sample (cm). Thus, OD260 has the units mL/cm.
Starting from the oligo molar extinction coefficient, ε260 :
- ε260 = L/(mol · cm) = 103 mL/(mol · cm) = mL/(mmol · cm)
Since OD260 has the units of mL/cm, the equation can be written as :
- 103 OD260/mol = 103 OD260 / 109 nmol = OD260 / 106 nmol
Combination of both equations yields :
- ε260 = OD260 / 106 nmol = OD260 / 103 umol = OD260 / mmol
Molecular Weight[4]
Molecular weight of an oligomer is a sum of the weights of individual bases and chemical modifications. Oligos are typically synthesized without 5’-phosphate group, which must be subtracted.
- MW = ΣIndividual Base MW + ΣIndividual Mod MW - PO2H + H2
where PO2H = 63.980 and H2 = 2.016
碱基 | 分子量 |
---|---|
MWdA | 313.209 |
MWdC | 289.184 |
MWdG | 329.208 |
MWdT | 304.196 |
MWdU | 290.169 |
引物合成报告的生成
以“5'-ACGT-3'的计算方法”为例[3]
第一步:计算消光系数
ε260 =(εAC+εCG+εGT)-(εC+εG) L ⋅ mol-1 ⋅ cm-1
ε260 = (21,200+18,000+20,000)-(7,400+11,500) L ⋅ mol-1 ⋅ cm-1
ε260 = 40,300 L ⋅ mol-1 ⋅ cm-1 = 40.3 L ⋅ mmol-1 ⋅ cm-1 = 40.3 OD260/umol
在所有网上技术信息和印刷的文件中,上述值40,300显示为40.3。这是因为单位是L ⋅ mmol-1 ⋅ cm-1(是毫摩尔而不是摩尔)。
第二步:计算浓度
A260设定为1.0光密度(OD)单位;
c = A/(ε * p)= 1/( 40,300 L ⋅ mol-1 ⋅ cm-1 * 1 cm) = 2.48*10-5 mol·L-1
第三步:计算摩尔质量(MW)
MW = [A x n+T x n+C x n+G x n]-PO2H + H2
MW = [313.209 x 1+289.184 x 1+329.208 x 1+304.196 x 1]- 63.980+2.016 = 1173.83 g·mol-1
第四步:将浓度换算为常用单位
c = 2.48 x 10-5 mol·L-1 x 1173.83 g·mol-1 = 29.1 ug·ml-1 = 29.1 ng·ul-1
引物酶标仪定量计算实例
引物信息如图:
![](https://img.haomeiwen.com/i19555511/64fb3fac380eb4cf.png)
将引物按理论值稀释至 100 uM,然后取1 uL加入至199 uL水中进行稀释,充分混匀,全部吸入透明96孔板中,用酶标仪进行测量,测得A 260为 0.4162 ,背景值为 0.0876 ;
引物实际摩尔浓度 c=(0.4162-0.0876)/(605.4 x 10-3) x 200 = 108.56 uM
接近理论值100 uM。
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