- ￥6300
- GeneTex
- 美国
- GTX60903
- 2025年07月13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 phospho-peptide corresponding to the Phospho-Histone H4 (pSer1).
- 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：
GTX60903
- 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 Histone H4 phosphorylated at Serine 1. The reactivity is not affected by neighboring Arginine 3 modifications. No cross reactivity with Histone H2A phosphorylated at Serine 1.
- 抗体英文名：
Histone H4S1ph (phospho Ser1) antibody [RM194]
- 抗体名：
Histone H4S1ph (phospho Ser1) 抗体 [RM194]
- 规格：
100 μg
WB analysis of extracts of HeLa cells (Lane 1) and recombinant Histone H4 protein (Lane 2) using GTX60903 Histone H4S1ph (phospho Ser1) antibody [RM194].
Dilution : 1μg/ml
ICC/IF analysis of HeLa cells using GTX60903 Histone H4S1ph (phospho Ser1) antibody [RM194].
Red : Primary antibody
Green : Actin
The GTX60903 reacts to Histone H4 phosphorylatedat Serine 1 (H4S1p). The reactivity is not affected byneighboring Arginine 3 modifications (H4S1pR3me1and H4S1pR3me2). No cross reactivity with Histone H2Aphosphorylated at Serine 1 (H2AS1p).
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文献和实验," made up of fragments of up to seven nucleosomes in length, is incubated with an antiserum directed against the histone modification of interest. The antibody-bound fraction is separated from the unbound fraction and, after extraction of genomic DNA from the bound
-phosphoserine的抗体。 摘抄： Anti-Phosphothreonine (MAb) - CryptateThe anti-phosphothreonine antibody is a monoclonal antibody (clone 42H4) produced at Cell Signaling Technology (reference 9386). It recognizes phosphorylated threonine residues in a manner
Chromatin Immunoprecipitation (ChIP)
of formaldehyde in the ChIP method was pioneered by Solomon and Varshavsky (Solomon et al. 1988). In their original studies, the association of histone H4 and RNA polymerase II with the Drosophila hsp70 genes was monitored. Cells were treated with formaldehyde
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