- ￥2890
- LSM Bio
- 0.15-10ng/ml
- 0.078mg/ml
- 国产
- CELI-66042h
- 2026年03月16日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
20
- 供应商：
LSMBIO
- 检测范围：
0.15-10ng/ml
- 检测方法：
夹心法/竞争法
- 应用：
夹心法/竞争法ELISA体外定量检测人血清、血浆或其它相关生物液体中蛋白浓度
- 适应物种：
人
- 标记物：
Cysteine, Cys
- 样本：
人血清、血浆或其它相关生物液体中天然和重组蛋白
- 灵敏度：
0.078mg/ml
- 规格：
96T
Human Cysteine, Cys ELISA Kit
96 Tests
Operating instructions
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE
BEGINNING!
Synonyms
Cysteine, Cys,C, 2-Amino-3-sulfhydrylpropanoic acid
Search name
Human Cysteine ELISA Kit, Human Cys ELISA Kit, Human 2-Amino-3-sulfhydrylpropanoic acid ELISA Kit, Human C ELISA Kit
Intended use
This immunoassay kit allows for the in vitro quantitative determination of Human cysteine,Cysteine concentrations in serum, plasma,
tissue homogenates, cell culture supernates, and other biological fluids.
Test principle
The ELISA is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in this kit has been
pre-coated with an antibody specific to Cysteine, During the reaction, Cysteine in the sample or standard competes with a fixed amount of
biotin-labeled Cysteine for sites on a pre-coated Monoclonal antibody specific to Cysteine. Excess conjugate and unbound sample or
standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and
incubated. Then a TMB substrate solution is added to each well. 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
Cysteine in the samples is then determined by comparing the O.D. of the samples to the standard curve.
PDF manual download
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文献和实验Fluorescent Labeling of Specific Cysteine Residues Using CyMPL
metal ions. Cys/His i+3 and Cys/His i+4 are helical peptides with histidines placed three and four positions away from a cysteine, respectively. HCN S563C,K565H depicts one β‐strand from the C‐terminal fragment of the mouse HCN2 ion channel
for the serodiagnosis of human fasciolosis. The methods illustrated in this chapter will explain the isolation of cysteine proteases from F. hepatica excretory-secretory products by gel filtration and anion exchange chromatography, and their subsequent characterization
有替代前者的趋势。由于ABS-ELISA较普通ELISA多用了两种试剂，增加了操作步骤，在临床检验中ABS-ELISA应用不多。科研项目中检测微量的成分如细胞因子常采用本法。晶美分装ELISA KIT采用的方法：1， TORCH及传染病试剂盒（间接法），见2.2.32， TORCH-IgM捕获法特色：包被抗体，标记抗原原理：3， 细胞因子试剂盒采用的方法路线（ABC-ELISA）原理产品特色：采用ABC法，灵敏度更高，特异性更强。生物素抗体和酶联物是浓缩的，使用前需用相应的缓冲液稀释。酶联物可以通用
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