ZNF828 抗体
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- 抗原 See all ZNF828 抗体
- ZNF828 (Zinc Finger Protein 828 (ZNF828))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This ZNF828 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ZNF828/C13orf8
- 亚型
- IgG
- Top Product
- Discover our top product ZNF828 Primary Antibody
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- ZNF828 (Zinc Finger Protein 828 (ZNF828))
- 别名
- ZNF828 (ZNF828 产品)
- 别名
- ZNF828 antibody, C13orf8 antibody, CAMP antibody, CHAMP antibody, AA675043 antibody, AI116001 antibody, D8Ertd457e antibody, D8Ertd569e antibody, Zfp828 antibody, Znf828 antibody, mKIAA1802 antibody, chromosome alignment maintaining phosphoprotein 1 antibody, CHAMP1 antibody, Champ1 antibody
- 背景
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Synonyms: chromosome 13 open reading frame 8, zinc finger protein 828, FLJ90413, KIAA1802, Zinc finger protein KIAA1802, CHAP1_HUMAN.
Background: Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZNF828, is a 812 amino acid protein that contains one C2H2-type zinc finger and is localized to the cytoplasm and the nucleus. The gene encoding ZNF828 maps to chromosome 13. Comprising nearly 4 % of the human genome, chromosome 13 contains around 114 million base pairs and encodes over 400 genes. Chromosome 13 houses key tumor suppressor genes, including BRCA2 and RB1, which are associated with breast cancer susceptibility and retinoblastoma, respectively. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
- 途径
- Maintenance of Protein Location
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