- ￥6300
- GeneTex
- 美国
- GTX33622
- 2025年07月15日
- WB, ICC/IF, ELISA
- Rabbit
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
A peptide corresponding to the C-terminus of human Histone macroH2A1.
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
- 克隆性：
Monoclonal
- 标记物：
Unconjugated
- 适应物种：
Human
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX33622
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB, ICC/IF, ELISA
- 浓度：
Batch dependent (Please refer to the vial label for the specific concentration.)
- 靶点：
This antibody reacts to the Core histone macro-H2A.1 and macro-H2A.2 proteins, independent of post-translational modifications. No cross reactivity with other histone proteins.
- 抗体英文名：
Macro H2A.1 antibody [RM248]
- 抗体名：
Macro H2A.1 抗体 [RM248]
- 规格：
100 μg
WB analysis of acid extracts from K562 cells using GTX33622 Macro H2A.1 antibody [RM248].
Dilution : 1μg/ml
ICC/IF analysis of HeLa cells using GTX33622 Macro H2A.1 antibody [RM248].
Red : Primary antibody
Green : Actin
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文献和实验[欢迎下载]：Antibody Engineering： Methods and Protocols
内容：Antibody Engineering： Methods and Protocols 格式：pdf 大小：5.18M 语种：英文 简介：为Methods in Molecular Biology系列第248卷，由Benny K. C. Lo主编，Humana Press 2003年出版。目录如下： 1 Internet Resources for the Antibody Engineer 2 The Kabat Database and a Bioinformatics
procedure for subtyping the NA glycoprotein is critical for the identification and classification of avian influenza (AI) viruses. The macro-procedure was first described in 1961 by D. Aminoff et al. [2 ] and was later modified to a microtiter plate
Evaluation of the Cardiac Isoform of 2-Macroglobulin as a Factor Inducing Cardiac Hypertrophy
is a cardiac isoform of α2 -macroglobulin belonging to the macro-globulin family. Furthermore, it has been demonstrated that direct injection of the purified 182-kDa protein intravenously (through the tail vein) into the normal animals led to the development
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