C9ORF57 抗体 (AA 61-160) (Biotin)
Quick Overview for C9ORF57 抗体 (AA 61-160) (Biotin) (ABIN1699949)
抗原
适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 61-160
-
预测反应
- Human
-
纯化方法
- Purified by Protein A.
-
免疫原
- KLH conjugated synthetic peptide derived from human C9orf57
-
亚型
- IgG
-
-
anti-Chromosome 9 Open Reading Frame 57 (C9ORF57) (AA 51-127) antibody
C9ORF57 适用: 人 ELISA, IHC 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
-
-
- C9ORF57 (Chromosome 9 Open Reading Frame 57 (C9ORF57))
-
别名
- C9orf57
-
背景
-
Synonyms: C9orf57, Chromosome 9 open reading frame 57, CI057_HUMAN, RP11-346E17.3, Uncharacterized protein C9orf57.
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 C9orf57 gene product has been provisionally designated C9orf57 pending further characterization.
-
基因ID
- 138240
抗原
-
