Anti-H2AX Antibody (CAB17425)
- SKU:
- CAB17425
- Product type:
- Antibody
- Reactivity:
- Oryza sativa
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
Frequently bought together:
Description
抗体名: | Anti-H2AX Antibody |
抗体コード: | CAB17425 |
抗体サイズ: | 20uL, 50 uL |
申し込み: | WB |
反応性: | Oryza sativa |
宿主種: | Rabbit |
免疫原: | A synthetic Peptide of Oryza sativa H2AX. |
申し込み: | WB |
推奨希釈: | WB 1:500 - 1:2000 |
反応性: | Oryza sativa |
ポジティブサンプル: |
免疫原: | A synthetic Peptide of Oryza sativa H2AX. |
精製方法: | Affinity purification |
ストレージバッファ: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
アイソタイプ: | IgG |
順序: | Email for sequence |
遺伝子ID: | 4333939 |
Uniprot: | Q8LLP5 |
セルラーロケーション: | |
計算された分子量: | 14kDa |
観察された分子量: | Refer to figures |
同義語: | H2AX |
バックグラウンド: |
UniProt Protein Function: | Variant histone H2A which replaces conventional H2A in a subset of nucleosomes. 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. Required for checkpoint-mediated arrest of cell cycle progression in response to low doses of ionizing radiation and for efficient repair of DNA double strand breaks (DSBs) specifically when modified by C-terminal phosphorylation. |
UniProt Code: | Q8LLP5 |
NCBI GenInfo Identifier: | 1002249421 |
NCBI Gene ID: | 4333939 |
NCBI Accession: | XP_015628892.1 |
UniProt Related Accession: | Q8LLP5 |
Molecular Weight: | 14kDa |
NCBI Full Name: | probable histone H2AXa |
NCBI Official Symbol: | LOC4333939 |
NCBI Official Synonym Symbols: | OsJ_011892 |
NCBI Protein Information: | probable histone H2AXa |
UniProt Protein Name: | Probable histone H2AXa |
UniProt Gene Name: | Os03g0721900 |