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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Synthetic phospho-peptide corresponding to residues surrounding Ser139 of human Histone H2A.X.
- 形态:
liquid
- 保存条件:
Store at -20˚C
- 克隆性:
Monoclonal
- 适应物种:
Human;Mouse;Rat
- 保质期:
12 months
- 抗原来源:
Recombinant Rabbit
- 供应商:
南京赛戈巍生物科技有限公司
- 宿主:
Recombinant Rabbit
- 应用范围:
WB;ICC/IF;IHC
- 靶点:
Uniprot:P16104
- 抗体英文名:
Histone H2A.X(Phospho-Ser139) Rabbit mAb
- 规格:
50ul/100ul
H2A histone family member X antibody
H2A.FX antibody
H2A.X antibody
H2a/x antibody
H2AFX antibody
H2AX antibody
H2AX histone antibody
H2AX_HUMAN antibody
Hist5.2ax antibody
Histone 2A antibody
Histone 2AX antibody
Histone H2A.X antibody
Histone H2AX antibody
RGD1566119 antibody
计算分子量:15 kDa
配方:1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide.
应用详情:WB: 1:500-1:2000
ICC/IF: 1:50-1:200
IHC: 1:50-1:200
图片:

Western blot analysis of Phospho-Histone H2A.X(S139) on HepG2 cell lysates using anti-Phospho-Histone H2A.X(S139) antibody at 1/1,000 dilution. Positive control:
Lane 1: HepG2 cell lysate?Ctreated with etoposide
Lane 3: HepG2 cell lysate?Cuntreated
,

Immunohistochemical analysis of paraffin-embedded mouse testis tissue using anti- Phospho-Histone H2A.X(S139) antibody. Counter stained with hematoxylin.
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文献和实验:使用 Anti-phospho-Akt (Ser473) Rabbit mAb 对石蜡包埋的人乳腺癌组织进行免疫组织化学分析。(图 A)使用免疫组化试剂盒M&R HRP/DAB Detection IHC Kit,抗体 1:100 稀释;(图 B) 采用普通免疫组化试剂盒,抗体 1:25 稀释。 图 6 免疫组化实验检测 Erk1/2 表达 注:使用 Anti-Erk1/2 Mouse mAb与p44/42 MAPK (Erk1/2)Rabbit mAb 对正常小鼠心脏组织进行免疫
TBS 和 5% NGS 中封闭样品。市售的含有酪蛋白的封闭溶液与磷酸化的一抗结合后易减弱信号;因此,我们建议不使用含有酪蛋白的封闭剂进行磷酸化特异性抗体的检测。以上针对封闭步骤所提建议均是在以 SignalStain. Boost IHC Detection Reagent 作为检测试剂的情况下提出的。如果选择使用其他检测试剂,我们则建议使用与二抗来源相同的血清进行封闭。抗体:Phospho–Histone H2A.X (Ser139) (20E3) Rabbit mAb #9718样本:石蜡
Competing Chromosomal Proteins from Drosophila Polytene Chromosomes Using Modified Histone Peptides
al ., 1996). In this adaptation, I used differently methylated histone tail peptides to compete Polycomb protein from polytene chromosomes, finding that competition was peptide specific and locus-specific (Ringrose et al ., 2004). (I also tried RNAse
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