常规试剂*：大龙移液器，Axygen耗材，康宁耗材,胰蛋白胨，封口膜，蛋白酶K，Trizol,B27,*佐剂，不*佐剂，四季青血清，细胞因子，ELISA试剂盒（免费代测一周内出结果），*，PVDF膜，NC膜，尼龙膜，滤器，X-Gluc，酵母粉，琼脂糖，蛋白酶K 朝霉素B，胶原酶 I II IV，G418，脂质体2000，等大量现货。
产品说明
eisa试剂盒:ELISA:试剂盒:酶联免疫试剂盒:KIT
eisa试剂盒:ELISA:试剂盒:酶联免疫试剂盒:KIT
保存条件及有效期：
1.试剂盒保存：；2-8℃。
2.有效期：6个月
1.试剂盒保存：；2-8℃。
2.有效期：6个月
适用标本:血浩、血桨、细胞焙养上清液、组织匀桨等
主要用途：科研检测
原理:双抗夹心法
试剂盒组成
1.标准品
2.标准品稀释浓
3.酶标包被板
4.链霉亲和素/HRP
5.20倍浓缩洗涤浓
6.显色剂A液
7.显色剂B液
8.终止液等
1.标准品
2.标准品稀释浓
3.酶标包被板
4.链霉亲和素/HRP
5.20倍浓缩洗涤浓
6.显色剂A液
7.显色剂B液
8.终止液等
需要而未提供的试剂和器材
1.37'C恒温箱。
2.标准规格酶标仪。
3.精密移液器及一次性吸头
4.蒸馏水
5一次性试管
6.吸水纸
1.37'C恒温箱。
2.标准规格酶标仪。
3.精密移液器及一次性吸头
4.蒸馏水
5一次性试管
6.吸水纸
注意事项
1.从2-8'C取出的试剂盒，在开启试剂盒之前要室温平衡至少30分钟.酶标包被板开封后如未用完，板条应装入密封袋中保存.
2.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.
3.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.
4.为避免交叉污染，要避免重复使用手中的吸头和封板膜.
5.不用的其它试剂应包装好或盖好.不同批号的试剂不要混用.保质前使用.
6.底物B对光敏感，避免长时间暴露于光下。
1.从2-8'C取出的试剂盒，在开启试剂盒之前要室温平衡至少30分钟.酶标包被板开封后如未用完，板条应装入密封袋中保存.
2.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.
3.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.
4.为避免交叉污染，要避免重复使用手中的吸头和封板膜.
5.不用的其它试剂应包装好或盖好.不同批号的试剂不要混用.保质前使用.
6.底物B对光敏感，避免长时间暴露于光下。
标本要求
1.不能检测含NaN3助样品，因NaN3抑制辣根过氧化物酶的〔HRP）活性。
2.标本采集后尽早进行提取，提取按相关文献进行，提取后应尽块进行实验.若不能马上进行试验，可将标本放于-20'C保存，但应避免反复冻融
1.不能检测含NaN3助样品，因NaN3抑制辣根过氧化物酶的〔HRP）活性。
2.标本采集后尽早进行提取，提取按相关文献进行，提取后应尽块进行实验.若不能马上进行试验，可将标本放于-20'C保存，但应避免反复冻融
样品收集、处理及保存方法:
1、血清……操作过程中避免任何细胞刺激.使用不含热原和内毒素的试管.收集血浓后，1000xg离心10分钟将血清和红细胞迅速小心地分离.
2、血浆......EDTA.柠檬酸盐、肝素血浆可用于检测.1000xg离心30分钟去除颗粒.
3.细胞上清液......1000 xg离心10分钟去除颗粒和聚合物.
4,组织匀浆……将组织加入适量生理盐水揭碎.1000xg离心10分钟，取上清液.
5.保存……如果样品不立即使用，应将其分成小部分-70'C保存，避免反复冷冻.尽可能的不要使用溶血或高血脂血.如果血清中大量颗粒，检测前先离心或过滤。不要在37'C或更高的温度加热解冻。应在室温下解冻并确保样品均匀地充分解冻。
1、血清……操作过程中避免任何细胞刺激.使用不含热原和内毒素的试管.收集血浓后，1000xg离心10分钟将血清和红细胞迅速小心地分离.
2、血浆......EDTA.柠檬酸盐、肝素血浆可用于检测.1000xg离心30分钟去除颗粒.
3.细胞上清液......1000 xg离心10分钟去除颗粒和聚合物.
4,组织匀浆……将组织加入适量生理盐水揭碎.1000xg离心10分钟，取上清液.
5.保存……如果样品不立即使用，应将其分成小部分-70'C保存，避免反复冷冻.尽可能的不要使用溶血或高血脂血.如果血清中大量颗粒，检测前先离心或过滤。不要在37'C或更高的温度加热解冻。应在室温下解冻并确保样品均匀地充分解冻。
具体详见说明书
Product Description
eisa kits: ELISA,: kits: ELISA kits: KIT
eisa kits: ELISA,: kits: ELISA kits: KIT
Storage conditions and duration of:
A kit to save:; 2-8 ° C.
Duration: 6 months
A kit to save:; 2-8 ° C.
Duration: 6 months
Applies to specimens: Hao of blood, plasma, cell baking raise the supernatant, the homogenate
Main purposes: scientific detection
Principle: the double-antibody sandwich method
Kit Contents
（1） standard
（2） Standard dilution of concentrated
3 ELISA coated plate
（4） streptavidin biotin / HRP
5.20 times concentrated washed concentrated
6. Color reagent A solution
7 color reagent B solution
8 Stop Solution
（1） standard
（2） Standard dilution of concentrated
3 ELISA coated plate
（4） streptavidin biotin / HRP
5.20 times concentrated washed concentrated
6. Color reagent A solution
7 color reagent B solution
8 Stop Solution
Without providing reagents and equipment
1.37 'C incubator.
Standard specifications microplate reader.
（3） precision pipette and the disposable tip
4. Distilled water
5 one-time test-tube
6. Absorbent paper
1.37 'C incubator.
Standard specifications microplate reader.
（3） precision pipette and the disposable tip
4. Distilled water
5 one-time test-tube
6. Absorbent paper
Note
（1） from 2-8'C remove the kit at room temperature before you open the kit balance of at least 30 minutes. ELISA plate coated plate after opening if not used, the lath should be stored in Sealed bag.
Each step of sample should be used pipette, and often proof of its accuracy, to avoid experimental error.
Strictly in accordance with the instructions of the operation, determine the test results to the microtiter plate reader as a standard.
In order to avoid cross-contamination, to avoid repeated use of the hands of the tip and the sealing plate membrane.
Without the other reagents should be packaged or covered. Do not mix different batches of reagents. Shelf life before use.
6. Substrate B is light sensitive, avoid prolonged exposure to light.
（1） from 2-8'C remove the kit at room temperature before you open the kit balance of at least 30 minutes. ELISA plate coated plate after opening if not used, the lath should be stored in Sealed bag.
Each step of sample should be used pipette, and often proof of its accuracy, to avoid experimental error.
Strictly in accordance with the instructions of the operation, determine the test results to the microtiter plate reader as a standard.
In order to avoid cross-contamination, to avoid repeated use of the hands of the tip and the sealing plate membrane.
Without the other reagents should be packaged or covered. Do not mix different batches of reagents. Shelf life before use.
6. Substrate B is light sensitive, avoid prolonged exposure to light.
Specimen requirements
Not detect samples containing NaN3 help because of NaN3 inhibition of horseradish peroxidase [HRP） activity.
2 specimen collection as soon as possible extraction, extraction by the relevant literature, due the blck after the extraction experiment. If it can not test the specimens were stored at-20'C, but should avoid repeated freezing and thawing
Not detect samples containing NaN3 help because of NaN3 inhibition of horseradish peroxidase [HRP） activity.
2 specimen collection as soon as possible extraction, extraction by the relevant literature, due the blck after the extraction experiment. If it can not test the specimens were stored at-20'C, but should avoid repeated freezing and thawing
Sample collection, processing and preservation methods:
Serum. Operation to avoid any cell stimulation. Pyrogen and endotoxin-free test tube to collect the blood concentration, 1000xg centrifugation for 10 minutes in serum and red blood cells rapidly and carefully isolated.
.1000 Xg for 30 minutes centrifugation, plasma ...... of EDTA. Citrate and heparin plasma can be used to detect the removal of particles.
Supernatant. 1,000 xg for centrifugal 10 minutes to remove particles and polymer.
Tissue homogenates. Will be organized by adding the appropriate amount of saline exposing broken .1000 xg for centrifuged for 10 minutes, and the supernatant.
Save ... If the sample is not used immediay, it should be divided into small part-70'C to save, to avoid repeated freezing as much as possible do not use hemolyzed or high lipid blood serum, a large number of particles, centrifugation or filtration prior to testing . Do not heated at 37'C or higher temperature to thaw. Should be thawed at room temperature and to ensure sample homogeneity fully thawed.
Serum. Operation to avoid any cell stimulation. Pyrogen and endotoxin-free test tube to collect the blood concentration, 1000xg centrifugation for 10 minutes in serum and red blood cells rapidly and carefully isolated.
.1000 Xg for 30 minutes centrifugation, plasma ...... of EDTA. Citrate and heparin plasma can be used to detect the removal of particles.
Supernatant. 1,000 xg for centrifugal 10 minutes to remove particles and polymer.
Tissue homogenates. Will be organized by adding the appropriate amount of saline exposing broken .1000 xg for centrifuged for 10 minutes, and the supernatant.
Save ... If the sample is not used immediay, it should be divided into small part-70'C to save, to avoid repeated freezing as much as possible do not use hemolyzed or high lipid blood serum, a large number of particles, centrifugation or filtration prior to testing . Do not heated at 37'C or higher temperature to thaw. Should be thawed at room temperature and to ensure sample homogeneity fully thawed.
免费代测 兔子前列腺素E2（PGE2）ELISA试剂盒 北京
全国： 刘 在线客服
环保在线