C9orf78 抗体 (AA 21-120) (AbBy Fluor® 350)
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- 抗原 See all C9orf78 (C9orf98) products
- C9orf78 (C9orf98) (Chromosome 9 Open Reading Frame 78 (C9orf98))
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抗原表位
- AA 21-120
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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 C9orf78 antibody is conjugated to AbBy Fluor® 350
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C9orf78
- 亚型
- IgG
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- C9orf78 (C9orf98) (Chromosome 9 Open Reading Frame 78 (C9orf98))
- 别名
- C9orf78 (C9orf98 产品)
- 别名
- HCA59 antibody, HSPC220 antibody, bA409K20.3 antibody, MGC84248 antibody, MGC186018 antibody, RP23-221O14.10 antibody, chromosome 9 open reading frame 78 antibody, chromosome 17 C9orf78 homolog antibody, chromosome 9 open reading frame 78 L homeolog antibody, zgc:103692 antibody, chromosome 9 C9orf78 homolog antibody, chromosome 11 open reading frame, human C9orf78 antibody, chromosome 9 open reading frame, human C9orf78 antibody, chromosome 17 open reading frame, human C9orf78 antibody, cDNA sequence BC005624 antibody, C9orf78 antibody, C17H9orf78 antibody, c9orf78.L antibody, zgc:103692 antibody, C9H9orf78 antibody, C11H9orf78 antibody, c9orf78 antibody, BC005624 antibody
- 背景
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Synonyms: bA409K20.3, C9orf78, Chromosome 9 open reading frame 78, CI078_HUMAN, HCA59, Hepatocellular carcinoma associated antigen 59, Hepatocellular carcinoma-associated antigen 59, HSPC220, Uncharacterized protein C9orf78.
Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered 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. The C9orf78 gene product has been provisionally designated C9orf78 pending further characterization.
- 基因ID
- 51759
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