Fanconi Anemia Complementation Group G (FANCG) (Middle Region) Peptide
FANCG
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all FANCG products
- FANCG (Fanconi Anemia Complementation Group G (FANCG))
- 蛋白结构域
- Middle Region
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 序列
- KSDAALQQLR AAALISRGLE WVASGQDTKA LQDFLLSVQM CPGNRDTYFH
- 产品特性
- This is a synthetic peptide designed for use in combination with anti- FANCG Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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- 应用备注
- Optimal working dilution should be determined by the investigator.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- FANCG (Fanconi Anemia Complementation Group G (FANCG))
- 别名
- xFANCG Peptide, FAG Peptide, XRCC9 Peptide, AU041407 Peptide, Xrcc9 Peptide, Fanconi anemia complementation group G S homeolog Peptide, Fanconi anemia complementation group G Peptide, Fanconi anemia, complementation group G Peptide, fancg.S Peptide, FANCG Peptide, Fancg Peptide
- 背景
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The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity, they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group G.
Alias Symbols: FAG, XRCC9
Protein Size: 622 - 基因ID
- 2189
- NCBI登录号
- NM_004629, NP_004620
- UniProt
- O15287
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