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- 详细信息
- 文献和实验
- 技术资料
- 库存:
50
- 供应商:
LSMBIO
- 检测范围:
78-5000pg/ml
- 检测方法:
夹心法
- 应用:
检测小鼠血清,血浆,组织匀浆等样本中目的蛋白的含量
- 适应物种:
小鼠
- 样本:
小鼠血清,血浆,组织匀浆
- 灵敏度:
46.79pg/ml
- 规格:
96tests
Mouse Growth arrest and DNA damage- inducible protein GADD45 gamma, GADD45G ELISA Kit
FOR RESEARCH USE ONLY!
96 Tests
Alternative name
Mouse GADD45G ELISA KIT ,Mouse CR6 ELISA KIT ,Mouse DDIT2 ELISA KIT ,Mouse GADD45gamma ELISA KIT ,Mouse GRP17 ELISA KIT ,Mouse growth arrest and DNA damage-inducible protein GADD45 gamma ELISA KIT ,Mouse DDIT-2 ELISA KIT ,Mouse DNA damage-inducible transcript 2 protein ELISA KIT ,Mouse GADD45-gamma ELISA KIT ,Mouse cytokine-responsive protein CR6 gadd-related protein 17 kD ELISA KIT ,Mouse growth arrest and DNA damage inducible gamma ELISA KIT
Intended use
Mouse GADD45G ELISA kit allows for the in vitro quantitative determination of Mouse GADD45G concentrations in serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.
Test principle
Mouse GADD45G ELISA kit Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for GADD45G and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain GADD45G, biotin-conjugated antibody and enzyme-conjugated Avidin 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 GADD45G in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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Although MDM2, the product of mouse double minute-2 (mdm2 ) gene, or its human homologue possesses the potential to confer tumorigenic properties, it induces G1/S arrest in nontransformed cells. Flow cytometry provides a way to determine
several assays for detecting several kinds of DNA damage (strand breaks, internal crosslinking, DNA/protein crosslinks) and repair activity following exposure to genotoxic agents. The methods include single?cell electrophoresis (comet assay), filter eluting, K
Electrophoretic Mobility Shift Analysis of the DNA Binding of Tumor Suppressor Gene Products
Central to the tumor suppressor activity of certain proteins is the ability to interact physically with DNA. A well-studied example of this is the tumor suppressor p53 (1 ,2 ). The p53 protein has been implicated in several diverse growth
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