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H3F3A (基因名), Histone H3.3 (蛋白名), h33_human.
产品名称:

Human H3F3A/ Histone H3.3 Recombinant Protein
组蛋白H3.3

货号:

R5810h

商标:
EIAab®
监管等级:
别名:

PP781, H3.3A, H3F3

序列号:
P84243
来源:
E.coli
种属:
Human
标签:
His
序列:
1-81aa
预估分子量:
8.91 kDa (monomer)
纯度:
Greater than 98% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
  • Human H3F3A Protein
  • Human H3F3A Protein
  • Human H3F3A Protein
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Human H3F3A Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
Human H3F3A Protein
The PCR product of human H3F3A gene was determined by 1% Agarose stained with EB.
Human H3F3A Protein
Recombinant human H3F3A protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 1q42.12 by HGNC 1q42.12 by Entrez Gene 1q42.12 by Ensembl
H3F3A Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
The nucleosome is a histone octamer containing two molecules each of H2A, H2B, H3 and H4 assembled in one H3-H4 heterotetramer and two H2A-H2B heterodimers. The octamer wraps approximately 147 bp of DNA. Interacts with HIRA, a chaperone required for its incorporation into nucleosomes. Interacts with ZMYND11; when trimethylated at 'Lys-36' (H3.3K36me3).


功能:
Variant histone H3 which replaces conventional H3 in a wide range of nucleosomes in active genes. Constitutes the predominant form of histone H3 in non-dividing cells and is incorporated into chromatin independently of DNA synthesis. Deposited at sites of nucleosomal displacement throughout transcribed genes, suggesting that it represents an epigenetic imprint of transcriptionally active chromatin. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling.


亚细胞位置:
Nucleus Chromosome


该产品尚未在任何出版物中被引用。

[1].
"The human replacement histone H3.3B gene (H3F3B)."

[2].
"Unusual structure, evolutionary conservation of non-coding sequences and numerous pseudogenes characterize the human H3.3 histone multigene family."

[3].
"Serine ADP-Ribosylation Depends on HPF1."

[4].
"ZMYND11 links histone H3.3K36me3 to transcription elongation and tumour suppression."

[5].
"Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone."

[6].
"The histone H3.3K27M mutation in pediatric glioma reprograms H3K27 methylation and gene expression."

[7].
"Inhibition of PRC2 activity by a gain-of-function H3 mutation found in pediatric glioblastoma."

[8].
"Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma."

[9].
"Organismal differences in post-translational modifications in histones H3 and H4."

[10].
"Identification of histone H3 lysine 36 acetylation as a highly conserved histone modification."
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