C22orf31 抗体
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- 抗原 See all C22orf31 products
- C22orf31 (Chromosome 22 Open Reading Frame 31 (C22orf31))
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适用
- 人
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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 C22orf31 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
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C22orf31
- 亚型
- IgG
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anti-Chromosome 22 Open Reading Frame 31 (C22orf31) (AA 113-162) antibody
C22orf31 适用: 人, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 22 Open Reading Frame 31 (C22orf31) (AA 71-120) antibodyC22orf31 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 22 Open Reading Frame 31 (C22orf31) (C-Term) antibodyC22orf31 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 22 Open Reading Frame 31 (C22orf31) (N-Term) antibodyC22orf31 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 22 Open Reading Frame 31 (C22orf31) (Middle Region) antibodyC22orf31 适用: 人, Cow, 犬, 马, Pig WB 宿主: 兔 Polyclonal unconjugated
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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
- C22orf31 (Chromosome 22 Open Reading Frame 31 (C22orf31))
- 别名
- C22orf31 (C22orf31 产品)
- 别名
- HS747E2A antibody, bK747E2.1 antibody, chromosome 22 open reading frame 31 antibody, C22orf31 antibody
- 背景
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Synonyms: HS747E2A, bK747E2.1, C22orf31, Chromosome 22 open reading frame 31, HS747E2A, Hypothetical protein LOC25770, CV031_HUMAN.
Background: C22orf31, also known as HS747E2A or bK747E2.1, is a 290 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
- 基因ID
- 25770
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