C9orf25 抗体 (AA 1-100) (Biotin)
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- 抗原 See all C9orf25 抗体
- C9orf25 (Chromosome 9 Open Reading Frame 25 (C9orf25))
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抗原表位
- AA 1-100
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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 C9orf25 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Sheep,Horse,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C9orf25
- 亚型
- IgG
- Top Product
- Discover our top product C9orf25 Primary Antibody
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anti-Chromosome 9 Open Reading Frame 25 (C9orf25) (AA 49-98) antibody
C9orf25 适用: 人, 小鼠, 大鼠, Cow, 斑马鱼, 犬, 豚鼠, 马, 兔, 非洲爪蟾, Bat, 小鸡, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 25 (C9orf25) (C-Term) antibodyC9orf25 适用: 人, 小鼠, 大鼠, Cow, 斑马鱼, 犬, 豚鼠, 马, 非洲爪蟾, Bat, 小鸡, 猴, 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
IHC-F 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
- 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
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- 抗原
- C9orf25 (Chromosome 9 Open Reading Frame 25 (C9orf25))
- 别名
- C9orf25 (C9orf25 产品)
- 别名
- C9orf25 antibody, bA573M23.5 antibody, C15H9orf25 antibody, 2310028H24Rik antibody, fam219a antibody, zgc:101028 antibody, family with sequence similarity 219 member A antibody, family with sequence similarity 219, member A antibody, family with sequence similarity 219, member Aa antibody, FAM219A antibody, Fam219a antibody, fam219aa antibody
- 背景
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Synonyms: bA573M23.5, C9orf25, Chromosome 9 open reading frame 25, F219A_HUMAN, FLJ39031, Hypothetical protein LOC203259, Uncharacterized protein C9orf25.
Background: C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. 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
- 203259
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