ZC3H7A 抗体
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- 抗原 See all ZC3H7A 抗体
- ZC3H7A (Zinc Finger CCCH-Type Containing 7A (ZC3H7A))
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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 ZC3H7A antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human ZC3H7A (NP_054872.2).
- 亚型
- IgG
- Top Product
- Discover our top product ZC3H7A Primary Antibody
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- 应用备注
- WB 1:500-1:2000 IF 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- ZC3H7A (Zinc Finger CCCH-Type Containing 7A (ZC3H7A))
- 别名
- ZC3H7A (ZC3H7A 产品)
- 别名
- zc3h7 antibody, fa12e01 antibody, fc07f05 antibody, fc38e12 antibody, fc55c11 antibody, zgc:55684 antibody, wu:fa12e01 antibody, wu:fc07f05 antibody, wu:fc38e12 antibody, wu:fc55c11 antibody, zc3hdc7 antibody, MGC81244 antibody, hspc055 antibody, A430104C18Rik antibody, AI447294 antibody, AW556219 antibody, HSPC055 antibody, Zc3h7 antibody, Zc3hdc7 antibody, ZC3H7 antibody, ZC3HDC7 antibody, zinc finger CCCH-type containing 7A antibody, zinc finger CCCH-type containing 7A L homeolog antibody, zinc finger CCCH type containing 7 A antibody, zc3h7a antibody, ZC3H7A antibody, zc3h7a.L antibody, Zc3h7a antibody
- 背景
- The zinc finger CCCH domain-containing protein 7A (ZC3H7A), also known as ZC3H7, HSPC055 or ZC3HDC7, is a 971 amino acid protein that contains a C3H1-type zinc finger domain, three C3H1-type zinc fingers and three TPR repeats. Belonging to the ZC3H12 family, ZC3H7A localizes to the nucleus. Existing as two alternatively spliced isoforms, ZC3H7A is encoded by a gene located on human chromosome 16p13.13. Chromosome 16 makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene.
- 分子量
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Observed_MW: 120kDa
Calculated_MW: 19kDa/110kDa
- 基因ID
- 29066
- UniProt
- Q8IWR0
- 途径
- SARS-CoV-2 Protein Interactome
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