C9orf78 抗体 (AA 21-120) (Biotin)
-
- 抗原 See all C9orf78 (C9orf98) products
- C9orf78 (C9orf98) (Chromosome 9 Open Reading Frame 78 (C9orf98))
-
抗原表位
- AA 21-120
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C9orf78 antibody is conjugated to Biotin
-
应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 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
-
anti-Chromosome 9 Open Reading Frame 78 (C9orf98) antibody
C9orf98 适用: 人 WB, IF, IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
-
- 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 for 12 months.
- 有效期
- 12 months
-
- 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
-
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
-
