C9orf169 抗体 (AA 1-100)
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- 抗原 See all C9orf169 (C9ORF169) products
- C9orf169 (C9ORF169) (Chromosome 9 Open Reading Frame 169 (C9ORF169))
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抗原表位
- AA 1-100
- 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 C9orf169 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunocytochemistry (ICC)
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C9orf169
- 亚型
- IgG
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anti-Chromosome 9 Open Reading Frame 169 (C9ORF169) (AA 1-144) antibody
C9ORF169 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4E4 unconjugated
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - 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
- C9orf169 (C9ORF169) (Chromosome 9 Open Reading Frame 169 (C9ORF169))
- 别名
- C9orf169 (C9ORF169 产品)
- 别名
- cysteine rich tail 1 antibody, CYSRT1 antibody
- 背景
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Synonyms: C9orf169, Chromosome 9 open reading frame 169, CI169_HUMAN, MGC59937, UPF0574 protein C9orf169.
Background: C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
- 基因ID
- 375791
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