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上海瑞齐生物科技有限公司作者
大鼠极低密度脂蛋白（ VLDL ）酶联免疫分析 试剂盒使用说明书
本试剂盒仅供研究使用。
检测范围：
96T
3μg/ml -120μg/ml
使用目的：
本试剂盒用于测定大鼠血清、血浆及相关液体样本中
极低密度脂蛋白
（
VLDL
）
含量。
实验原理
本试剂盒应用双抗体夹心法测定标本中大鼠极低密度脂蛋白
（
VLDL
）水平。用纯化的大鼠极低密度脂蛋白
（
VLDL
）抗体包被微孔板，制成固相抗体，往包被单抗的微孔中依次加入极低密度脂蛋白
（
VLDL
）
，再与HRP标记的极低密度脂蛋白
（
VLDL
）抗体结合，形成抗体-抗原-酶标抗体复合物，经过*洗涤后加底物TMB显色。TMB在HRP酶的催化下转化成蓝色，并在酸的作用下转化成zui终的黄色。颜色的深浅和样品中的极低密度脂蛋白
（
VLDL
）呈正相关。用酶标仪在450nm波长下测定吸光度（OD值），通过标准曲线计算样品中大鼠极低密度脂蛋白
（
VLDL
）浓度。
试剂盒组成
|
1
|
30倍浓缩洗涤液
|
20ml×1瓶
|
7
|
终止液
|
6ml×1瓶
|
|
2
|
酶标试剂
|
6ml×1瓶
|
8
|
标准品（240μg/ml）
|
0.5ml×1瓶
|
|
3
|
酶标包被板
|
12孔×8条
|
9
|
标准品稀释液
|
1.5ml×1瓶
|
|
4
|
样品稀释液
|
6ml×1瓶
|
10
|
说明书
|
1份
|
|
5
|
显色剂A液
|
6ml×1瓶
|
11
|
封板膜
|
2张
|
|
6
|
显色剂B液
|
6ml×1/瓶
|
12
|
密封袋
|
1个
|
标本要求
1．标本采集后尽早进行提取，提取按相关文献进行，提取后应尽快进行实验。若不能马上进行试验，可将标本放于-20℃保存，但应避免反复冻融
2．不能检测含NaN3的样品，因NaN3抑制辣根过氧化物酶的（HRP）活性。
操作步骤
1.
标准品的稀释：本试剂盒提供原倍标准品一支，用户可按照下列图表在小试管中进行稀释。
|
120μg/ml
|
5号标准品
|
150μl的原倍标准品加入150μl标准品稀释液
|
|
60μg/ml
|
4号标准品
|
150μl的5号标准品加入150μl标准品稀释液
|
|
30μg/ml
|
3号标准品
|
150μl的4号标准品加入150μl标准品稀释液
|
|
15μg/ml
|
2号标准品
|
150μl的3号标准品加入150μl标准品稀释液
|
|
7.5μg/ml
|
1号标准品
|
150μl的2号标准品加入150μl标准品稀释液
|
2.
加样：分别设空白孔（空白对照孔不加样品及酶标试剂，其余各步操作相同）、标准孔、待测样品孔。在酶标包被板上标准品准确加样50μl，待测样品孔中先加样品稀释液40μl，然后再加待测样品10μl（样品zui终稀释度为5倍）。加样将样品加于酶标板孔底部，尽量不触及孔壁，轻轻晃动混匀。
3.
温育：用封板膜封板后置37℃温育30分钟。
4.
配液：将30倍浓缩洗涤液用蒸馏水30倍稀释后备用
5.
洗涤：小心揭掉封板膜，弃去液体，甩干，每孔加满洗涤液，静置30秒后弃去，如此重复5次，拍干。
6.
加酶：每孔加入酶标试剂50μl，空白孔除外。
7.
温育：操作同3。
8.
洗涤：操作同5。
9.
显色：每孔先加入显色剂A50μl，再加入显色剂B50μl，轻轻震荡混匀，37℃避光显色15分钟.
10.
终止：每孔加终止液50μl，终止反应（此时蓝色立转黄色）。
11.
测定：以空白空调零，450nm波长依序测量各孔的吸光度（OD值）。 测定应在加终止液后15分钟以内进行。
操作程序总结：
计算
以标准物的浓度为横坐标，OD值为纵坐标，在坐标纸上绘出标准曲线，根据样品的OD值由标准曲线查出相应的浓度；再乘以稀释倍数；或用标准物的浓度与OD值计算出标准曲线的直线回归方程式，将样品的OD值代入方程式，计算出样品浓度，再乘以稀释倍数，即为样品的实际浓度。
注意事项
1．试剂盒从冷藏环境中取出应在室温平衡15-30分钟后方可使用，酶标包被板开封后如未用完，板条应装入密封袋中保存。
2．浓洗涤液可能会有结晶析出，稀释时可在水浴中加温助溶，洗涤时不影响结果。
3．各步加样均应使用加样器，并经常校对其准确性，以避免试验误差。一次加样时间控制在5分钟内，如标本数量多，推荐使用排枪加样。
4．请每次测定的同时做标准曲线，做复孔。如标本中待测物质含量过高（样本OD值大于标准品孔*孔的OD值），请先用样品稀释液稀释一定倍数（n倍）后再测定，计算时请zui后乘以总稀释倍数（×n×5）。
5．封板膜只限一次性使用，以避免交叉污染。
6．底物请避光保存。
7．严格按照说明书的操作进行，试验结果判定必须以酶标仪读数为准.
8．所有样品，洗涤液和各种废弃物都应按传染物处理。
9．本试剂不同批号组分不得混用。
10. 如与英文说明书有异，以英文说明书为准。
保存条件及有效期
1．试剂盒保存：；2-8℃。
2．有效期：6个月
|
RD
|
FOR RESEARCH USE ONLY
Assay range
：
3μg/mL
–
120
μg/mL
96
determinations
Purpose
This kit allows for the
determination of
VLDL concentrations
in
Rat
serum,
cell
culture supernates
and other
biological fluids
Principle of the assay
T
he kit
assay
Rat
VLDL
level in the
sample
，
use
Purified
Rat
VLDL
antibody to coat
microtiter plate wells
, make
solid-phase antibody, then add
VLDL
to
wells
,
Combined
VLDL
antibody which With HRP labeled
,
become
antibody - antigen - enzyme-antibody complex, after
washing
Compley,
Add TMB substrate solution,TMB substrate becomes blue color At HRP enzyme-catalyzed,
reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm.
The concentration of
Rat
VLDL
in the samples is then determined by comparing the O.D. of the samples to the standard curve
.
Materials provided with the k
it
|
1
|
wash solution
|
2
0ml×1bottle
|
7
|
Stopp Solution
|
6
ml×1 bottle
|
|
2
|
HRP-Conjugate reagent
|
6
ml×1 bottle
|
8
|
Standard
（240μg/ml）
|
0.5ml×1 bottle
|
|
3
|
Microelisa stripplate
|
12well×
8
strips
|
9
|
Standard diluent
|
1.5
ml×1bottle
|
|
4
|
Sample diluent
|
6
ml×1 bottle
|
10
|
Instruction
|
1
|
|
5
|
Chromogen Solution A
|
6
ml×1 bottle
|
11
|
Closure plate membrane
|
2
|
|
6
|
Chromogen Solution B
|
6
ml×1 bottle
|
12
|
Sealed bags
|
1
|
Specimen requirements
1.
extract
as soon as possible after Specimen collection,
and
according to the relevant literature, and should be
experiment as soon as possible after the extraction.
If it can
’t,
specimen can be kept in -20
℃
to preserve, Avoid repeated freeze-thaw cycles
.
2.
Can’t detect the sample which contain
NaN3, because
NaN3
inhibits
HRP active.
Assay procedure
1.
Dilute and add sample:Dilute
Original density
Standard as follow table:
|
120μg/ml
|
5
Standard
|
150μl
Original density
Standard+150μl
Standard diluent
|
|
80μg/mL
|
4
Standard
|
150μl
5 Standard+150μl
Standard diluent
|
|
40μg/mL
|
3
Standard
|
150μl 4
Standard+150μl
Standard diluent
|
|
20μg/mL
|
2
Standard
|
150μl 3
Standard
+150μl
Standard diluent
|
|
10μg/mL
|
1
Standard
|
150μl 2
Standard
+150μl
Standard diluent
|
2.add sample
：
Set blank wells separay （blank comparison wells don’t add sample and
HRP-Conjugate reagent
, other each step operation is same）. testing sample well. add Sample dilution 40μl to testing sample well
, then add
testing sample 10μl （
sample final dilut
ion
is 5
-fold）,
add sample to
well
s
,
don’t touch the well wall as far as possible,
and
Gently mix.
3.Incubate: After closing plate with
Closure plate membrane ,incubate for 30 min at
37
℃
.
4.Configurate liquid: 30-fold（or 20-fold）
wash solution
diluted 30-fold （or 20-fold） with distilled water and reserve.
5.washing
：
Uncover
Closure plate membrane,
discard
Liquid, dry by swing, add washing buffer to every well, still for 30s then drain,
repeat 5 times, dry by pat.
6.add enzyme
：
Add
HRP-Conjugate reagent
50μl to each well, except blank well.
7.incubate
：
Operation with 3.
8.washing
：
Operation with 5.
9.
color
：
Add
Chromogen Solution A
50ul and
Chromogen Solution
B to each well,
evade the light preservation
for 15 min at 37
℃
10.
Stop the reaction
：
Add
Stop Solution
50μl
to each well, Stop the reaction（the blue color change to yellow color）.
11.
assay
：
take blank well as zero ,
Read absorbance at 450nm
after
Adding
Stop Solution and within 15min.
Steps description
|
Standard,
Sample diluent
|
|
Add
Standard,
Sample diluent
,
incubate for 30 min at
37
℃
.
|
|
Wash 5 time,Add
HRP-Conjugate reagent, incubate for 30 min at
37
℃
.
|
|
Wash 5 times,Add Chromogen Solution A
and B,
incubate for 30 min at
37
℃
.
|
|
Add
Stopp Solution
|
|
Read absorbance at 450nm within 15 min
|
|
calculate
|
Calculate
Take the standard density as the
horizontal
, the OD value for the
vertical
,draw the standard curve on
graph paper,
Find out the corresponding density according to the sample OD value by the Sample curve, multiplied by the dilution multiple, or calculate the straight line regression equation of the standard curve with the standard density and the OD value ,with the sample OD value in the equation, calculate the sample density, multiplied by the dilution
factor
, the result is the sample actual density.
Important notes
1.
The kit takes out from the refrigeration environment should be balanced 15-30 minutes in the room temperature,
ELISA plates coated if has not use up after opened, the plate should be stored in Sealed bag.
2.
washing buffer will Crystallization separation, it can be heated the water helps dissolve when dilute . Washing does not affect the result.
3.
add Sample with sampler Each step, And proofread its accuracy frequently, avoids the experimental error. add sample within 5 min, if the number of sample is much , recommend to use Volley .
4.
if the testing material content is excessively high
er
（The sample OD is bigger than the first standard well ）,please dilute Sample （n
-fold
）, Please diluent
e
and
multiplied by the dilution
factor.
（
×n×5
）
.
5.
Closure plate membrane
only limits the disposable use, to avoid
cross-contamination
.
6.
The substrate evade the light preservation.
7.
Please according to use instruction strictly, The test result determination must take the
microtiter plate reader
as a standard.
8.
All samples, washing buffer and each kind of reject should according to infective material process.
9.
Do not mix reagents with those from other lots
.
Storage and validity
1
．
Storage
：
2-8
℃
.
2
．
validity
：
six months
关键词：酶标仪
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