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小鼠(INS)小鼠胰岛素(INS)ELISA试剂盒说明书
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Mouse Insulin (INS)ELISA Kit
Catalog No. CSB-E05071m
(96T)
This immunoassay kit allows for the in vitro quantitative determination of mouse INS
concentrations in serum, plasma and other biological fluids.
Expiration date six months from the date of manufacture
FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES.
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INTRODUCTION
Insulin is a peptide hormone composed of 51 amino acid residues and has a
molecular weight of 5808 Da. It is produced in the islets of Langerhans in the
pancreas. Insulin’s structure varies slightly between species of animal. Insulin
has extensive effects on both metabolism and several other body systems (eg,
vascular compliance). Insulin causes most of the body’s cells to take up
glucose from the blood (including liver, muscle, and fat tissue cells), storing it
as glycogen in the liver and muscle, and stops use of fat as an energy source.
When insulin is absent (or low), glucose is not taken up by most body cells and
the body begins to use fat as an energy source (ie, transfer of lipids from
adipose tissue to the liver for mobilization as an energy source). As its level is
a central metabolic control mechanism, its status is also used as a control
signal to other body systems (such as amino acid uptake by body cells). It has
several other anabolic effects throughout the body.
PRINCIPLE OF THE ASSAY
The microtiter plate provided in this kit has been pre-coated with an antibody
specific to INS. Standards or samples are then added to the appropriate
microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated
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monoclonal antibody preparation specific for INS and incubated. Then
substrate solution A and B are added to each well. Only those wells that
contain INS, HRP-conjugated antibody will exhibit a change in color. The
enzyme-substrate reaction is terminated by the addition of a sulphuric acid
solution and the color change is measured spectrophotometrically at a
wavelength of 450 nm ± 2 nm. The concentration of INS in the samples is then
determined by comparing the O.D. of the samples to the standard curve.
DETECTION RANGE
8μIU/ml-140μIU/ml. The standard curve concentrations used for the ELISA’s
were 140μIU/ml,80μIU/ml,32μIU/ml, 16μIU/ml, 8μIU/ml
SPECIFICITY
This assay recognizes recombinant and natural mouse INS. No significant
cross-reactivity or interference was observed.
SENSITIVITY
The minimum detectable dose of mouse INS is typically less than 5μIU/ml.
The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as
the lowest concentration that could be differentiated from zero.
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MATERIALS PROVIDED
Reagent Quantity
Assay plate 1
Standard(S -S ) 5
1 5
HRP-conjugate 1 x 6 ml
1 x 15 ml
Wash Buffer
(20×concentrate)
Substrate A 1 x 7 ml
Substrate B 1 x 7 ml
Stop Solution 1 x 7 ml
Standard Standard Standard Standard Standard
Standard
1 2 3 4 5
Concentration
8 16 32 80 140
(μIU/ml)
STORAGE
1. Unopened test kits should be stored at 2-8°C upon receipt and the
microtiter plate should be kept in a sealed bag to minimize exposure to
damp air. The test kit may be used throughout the expiration date of the kit.
Refer to the package label for the expiration date.
2. Opened test kits will remain stable until the expiring date shown, provided it
is stored as prescribed above.
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3. A microtiter plate reader with a bandwidth of 10 nm or less and an optical
density range of 0-3 OD or greater at 450nm wavelength is acceptable for
use in absorbance measurement.
REAGENT PREPARATION
1. Bring all reagents and plate to room temperature for at least 30 minutes
before use. Unused wells need store at 2-8°C and av oid sunlight.
2. Wash Buffer If crystals have formed in the concentrate, warm to room
temperature and mix gently until the crystals have completely dissolved.
Dilute 15 ml of Wash Buffer Concentrate into deionized or distilled water to
prepare 300 ml of Wash Buffer.
Precaution: The Stop Solution provided with this kit is an acid solution. Wear eye,
hand, face, and clothing protection when using this material.
OTHER SUPPLIES REQUIRED
Microplate reader capable of measuring absorbance at 450 nm, with the
correction wavelength set at 540 nm or 570 nm.
Pipettes and pipette tips.
Deionized or distilled water.
Squirt bottle, manifold dispenser, or automated microplate washer.
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SAMPLE COLLECTION AND STORAGE
Serum Use a serum separator tube (SST) and allow samples to clot for
30 minutes before centrifugation for 15 minutes at 1000 g. Remove serum
and assay immediately or aliquot and store samples at -20° C. Avoid
repeated freeze-thaw cycles.
Plasma Collect plasma using citrate, EDTA, or heparin as an
anticoagulant. Centrifuge for 15 minutes at 1000 g within 30 minutes of
collection. Assay immediately or aliquot and store samples at -20°C. Avoid
repeated freeze-thaw cycles.
Note: Grossly hemolyzed samples are not suitable for use in this assay.
ASSAY PROCEDURE
Bring all reagents and samples to room temperature before use. It is recommended
that all samples, standards, and controls be assayed in duplicate.
1. Set a Blank well without any solution. Add 50μl of Standard or Sample per
well. Standard need test in duplicate.
2. Reconstitute the every Standard with 0.5 ml of distilled water.
3. Add 50μl of HRP-conjugate to each well (not to Blank well). Mix well and
then incubate for 2 hour at 37°C.
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4. Complete remove the liquid. Then fill each well with Wash Buffer (about
200μl), stay for 10 seconds and Spinning. Repeat the process for a total of
three washes. Complete removal of liquid at each step is essential to good
performance. After the last wash, remove any remaining Wash Buffer by
aspirating or decanting. Invert the plate and blot it against clean paper
towels.
5. Add 50μl of Substrate A and 50μl of Substrate B to each well, mix well.
Incubate for 15 minutes at 37°C. Keeping the plate away from drafts and
other temperature fluctuations in the dark.
6. Add 50μl of Stop Solution to each well. If color change does not appear
uniform, gently tap the plate to ensure thorough mixing.
7. Determine the optical density of each well within 10 minutes, using a
microplate reader set to 450 nm.
CALCULATION OF RESULTS
Average the duplicate readings for each standard, control, and sample and
subtract the average zero standard optical density. Create a standard curve by
reducing the data using computer software capable of generating a four
parameter logistic (4-PL) curve-fit. As an alternative, construct a standard
curve by plotting the mean absorbance for each standard on the y-axis against
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the concentration on the x-axis and draw a best fit curve through the points on
the graph. The data may be linearized by plotting the log of the INS
concentrations versus the log of the O.D. and the best fit line can be
determined by regression analysis. This procedure will produce an adequate
but less precise fit of the data. If samples have been diluted, the concentration
read from the standard curve must be multiplied by the dilution factor.
LIMITATIONS OF THE PROCEDURE
The kit should not be used beyond the expiration date on the kit label.
Do not mix or substitute reagents with those from other lots or sources.
It is important that the Calibrator Diluent selected for the standard curve be
consistent with the samples being assayed.
If samples generate values higher than the highest standard, dilute the
samples with the appropriate Calibrator Diluent and repeat the assay.
Any variation in Standard Diluent, operator, pipetting technique, washing
technique, incubation time or temperature, and kit age can cause variation
in binding.
This assay is designed to eliminate interference by soluble receptors,
binding proteins, and other factors present in biological samples. Until all
factors have been tested in the Quantikine Immunoassay, the possibility of
interference cannot be excluded.
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TECHNICAL HINTS
When mixing or reconstituting protein solutions, always avoid foaming.
To avoid cross-contamination, change pipette tips between additions of
each standard level, between sample additions, and between reagent
additions. Also, use separate reservoirs for each reagent.
When using an automated plate washer, adding a 30 second soak period
following the addition of wash buffer, and/or rotating the plate 180 degrees
between wash steps may improve assay precision.
To ensure accurate results, proper adhesion of plate sealers during
incubation steps is necessary.
Substrate Solution should remain colorless until added to the plate. Keep
Substrate Solution protected from light. Substrate Solution should change
from colorless to gradations of blue.
Stop Solution should be added to the plate in the same order as the
Substrate Solution. The color developed in the wells will turn from blue to
yellow upon addition of the Stop Solution. Wells that are green in color
indicate that the Stop Solution has not mixed thoroughly with the Substrate
Solution.
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小鼠小鼠胰岛素胰岛素 （（Insulin））ELISA 快速检测试剂盒快速检测试剂盒
小小鼠鼠胰岛素胰岛素 （（ ）） 快速检测试剂盒快速检测试剂盒
使用说明书使用说明书
使用说明书使用说明书
本试剂盒仅供研究使用本试剂盒仅供研究使用
本试剂盒仅供研究使用本试剂盒仅供研究使用
产品编号产品编号：CSB-E05071m
产品编号产品编号
检测范围检测范围：：8μIU /ml -140μIU /ml
检测范围检测范围：：
特异性特异性：：本试剂盒可同时检测天然或重组的 INS，且与其他相关蛋白基本无
特异性特异性：：
交叉反应。
有效期有效期：6 个月 （2-8℃避光保存）
有效期有效期
预期应用预期应用：：ELISA 法定量测定小鼠血清，血浆及其它相关生物液体中INS 含
预期应用预期应用：：
量。
说明说明
说明说明
1. 浓洗涤液低温保存会有盐析出，稀释时可在水浴中加温助溶。
2. 刚开启的酶联板孔中可能会含有少许水样物质，此为正常现象，不会对实验
结果造成任何影响。
实验原理实验原理
实验原理实验原理
采用酶联免疫法夹心法检测胰岛素含量。首先用一株单抗体包被微孔板，
制备成固相抗体，然后加入待测标本及辣根过氧化物酶标记的另一株单抗，使
之形成包被抗体-胰岛素-酶标记抗体的复合物。经显色后在酶标仪测定吸光值
（OD 值），通过计算机或作图拟合浓度-吸光度曲线，反算出待测标本中胰岛素
含量。
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试剂盒组成及试剂配制试剂盒组成及试剂配制
试剂盒组成及试剂配制试剂盒组成及试剂配制
1. 酶联板酶联板(Assay plate )： 一块（96 孔）。
酶联板酶联板
2. 标准品标准品（Standard）： 5 瓶（冻干品）。
标准品标准品
Standard 1 Standard 2 Standard 3 Standard 4 Standard 5
8μIU/ml 16μIU/ml 32μIU/ml 80μIU/ml 140μIU/ml
3. 酶结合物酶结合物（（HRP-conjugate）：） 1×6ml/瓶。
酶结合物酶结合物（（ ））
4. 显色剂显色剂A （（Substrate A）：）： 1×7ml/瓶。
显色剂显色剂 （（ ）：）：
5. 显色剂显色剂B （（Substrate B）：）： 1×7ml/瓶。
显色剂显色剂 （（ ）：）：
6. 浓洗涤液浓洗涤液（（Wash Buffer ）：） 1×15ml/瓶，使用时每瓶用蒸馏水稀释20 倍。
浓洗涤液浓洗涤液（（ ））
7. 终止液终止液（（Stop Solution）：） 1×7ml/瓶
终止液终止液（（ ））
需要而未提供的试剂和器材需要而未提供的试剂和器材
需要而未提供的试剂和器材需要而未提供的试剂和器材
1. 标准规格酶标仪
2. 高速离心机
3. 电热恒温培养箱
4. 干净的试管和Eppendof 管
5. 系列可调节移液器及吸头，一次检测样品较多时，最好用多通道移液器
6. 蒸馏水，容量瓶等
标本的标本的采集及保存采集及保存
标本的标本的采集及保存采集及保存
1. 血清：全血标本请于室温放置2 小时或4℃过夜后于1000 x g 离心20 分钟，
取上清即可检测，或将标本放于-20℃或-80℃保存，但应避免反复冻融。
2. 血浆：可用EDTA 或肝素作为抗凝剂，标本采集后30 分钟内于2 - 8° C 1000
x g 离心15 分钟，或将标本放于-20℃或-80℃保存，但应避免反复冻融。
3. 细胞培养物上清或其它生物标本：1000 x g 离心20 分钟，取上清即可检测，
或将标本放于-20℃或-80℃保存，但应避免反复冻融。
注：注：以上标本置以上标本置4℃℃保存应小于保存应小于1 周，周，-20℃℃或或-80℃℃均应密均应密封保存封保存，，-20℃℃不应超过不应超过1 个月个月，，
注注：：以上标本置以上标本置 ℃℃保存应小于保存应小于 周周，， ℃℃或或 ℃℃均应密均应密封保存封保存，， ℃℃不应超过不应超过 个月个月，，
-80℃℃不应超过不应超过2 个月个月；标本溶血会影响最后检测结果；标本溶血会影响最后检测结果，因此溶血标本不宜进行此项检测，因此溶血标本不宜进行此项检测。。
℃℃不应超过不应超过 个月个月；；标本溶血会影响最后检测结果标本溶血会影响最后检测结果，，因此溶血标本不宜进行此项检测因此溶血标本不宜进行此项检测。。
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操作步骤操作步骤
操作步骤操作步骤
1. 将各种试剂至室温 〔18-25℃〕平衡半小时，取浓缩洗涤液，根据当批检测
数量，用蒸馏水上1：20 稀释，混匀后备用。
2. 标准品S1- S 5，第一次使用前先用0.5ml 蒸馏水溶解，放置混匀后使用。
3. 将酶标板取出，设一个空白对照孔、不加任何液体；每个标准点依次各设两
孔，每孔加入相应标准品50ul；其余每个检测孔直接加待测标本50ul。
4. 每孔加入酶结合物50ul （空白对照孔除外），充分混匀，贴上不干胶封片，
置37℃温育2 小时。
5. 手工洗板，弃去孔内液体。洗涤液注满各孔，静置10 秒甩干，重复三次后
拍干；洗板机洗板，选择洗涤三次程序，洗板后拍干。
6. 每孔加显色剂A 液50μl，显色剂B 液50μl，振荡混匀后，37℃避光显色15
分钟，每孔加终止液50μl。
7. 用酶标仪读数，取波长450nm，先用空白孔调零点，然后测定各孔OD 值。
数据处理数据处理
数据处理数据处理
1. 手工作图：用双对数坐标纸，以标准品浓度为横轴，以对应的0D 值为纵轴，
画出平滑曲线或直线，在曲线上按照待测血清OD 值找到对应的浓度值。
2. 计算机：使用线性拟合功能，应将标准品S1-S5 的浓度取对数（Log(浓度)）
作为X，将对应的OD 值减去空白对照孔OD 值后取对数（Log(OD 值-NSB)）
作为Y，进行线性拟合。再从拟合线上计算出待测血清浓度。
注意事项注意事项
注意事项注意事项
1. 从冷藏环境中取出的试剂盒内全部瓶装试剂及所需预包被板条应置室温
（18-25℃）平衡30 分钟后方可使用，余者应及时封好口，放回2-8℃中避光保
存，以备后用。
2. 使用前试剂应摇匀。
3. 结果判断须在反应终止后10 分钟内完成。
4. 不同批号的试剂不可混用。
5. 加样时应注意避免所用各试剂及样品之间的交又污染。
6. 操作时，试剂盒内每种试剂各使用一个吸头，每一种标准品使用一个吸头，
每一个样品各使用一个吸头，吸头最好一次性使用。
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Notes
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