推荐产品
生物来源
mouse
偶联物
peroxidase conjugate
抗体形式
purified immunoglobulin
抗体产品类型
secondary antibodies
克隆
MAH 1.12, monoclonal
表单
lyophilized powder
种属反应性
hamster
请勿与下列物质发生反应
rat, bovine, horse, chicken, goat, human, mouse, pig, rabbit
技术
direct ELISA: 1:40,000 using hamster IgG as the coating protein
western blot: 1:2,000 using recombinant mouse TNFα
同位素/亚型
IgG2b
运输
wet ice
储存温度
−20°C
靶向翻译后修饰
unmodified
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一般描述
IgGs are glycoprotein antibodies that modulate several immune responses. Hamster IgGs against target proteins are often used as primary antibodies in various research applications. Thus, secondary anti-hamster IgGs conjugated to a detectable substrate are useful tools for the analysis of target proteins. Mouse Monoclonal Anti-hamster IgG-Peroxidase antibody is immunospecific for hamster IgG and does not recognize human, bovine, horse, goat, pig, rabbit, rat, mouse, and chicken IgG.
免疫原
purified Armenian hamster monoclonals (TN3-19.2 and H22).
应用
Mouse Monoclonal Anti-Hamster IgG-Peroxidase antibody is suitable for ELISA (1:40,000) and western blotting (1:2,000) applications.
Parasite cell lysates were analyzed by western blot using goat anti-hamster IgG at a 1:5000 dilution for 1 hour at room temperature.
外形
Lyophilized powder containing 0.01 M phosphate buffered saline, pH 7.4, 1% bovine serum albumin, and 0.01% merthiolate.
免责声明
For U.S. Customers: Contains mercury; Do not place in trash - dispose according to local, state, or federal laws.
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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储存分类代码
13 - Non Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
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Infection and immunity, 72(4), 2194-2202 (2004-03-25)
Several Leishmania proteins have been identified and characterized in pursuit of understanding pathogenesis and protection in cutaneous leishmaniasis. In the present study, we utilized sera from infected BALB/c mice to screen a Leishmania amazonensis amastigote cDNA expression library and obtained
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