C9orf96 抗体 (AA 101-200)
Quick Overview for C9orf96 抗体 (AA 101-200) (ABIN1713457)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 101-200
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交叉反应
- 人
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human C9orf96
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亚型
- IgG
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anti-Chromosome 9 Open Reading Frame 96 (C9orf96) (AA 1-99) antibody
C9orf96 适用: 人 WB, ELISA, RNAi 宿主: 小鼠 Monoclonal 2B5 unconjugated
anti-Chromosome 9 Open Reading Frame 96 (C9orf96) (AA 1-680) antibodyC9orf96 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 96 (C9orf96) (C-Term) antibodyC9orf96 适用: 人 WB, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 96 (C9orf96) (AA 581-630) antibodyC9orf96 适用: 人, Cow, 犬 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 96 (C9orf96) (AA 137-165), (N-Term) antibodyC9orf96 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB35094 unconjugated
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应用备注
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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
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- C9orf96 (Chromosome 9 Open Reading Frame 96 (C9orf96))
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别名
- C9orf96
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背景
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Synonyms: Chromosome 9 open reading frame 96, Hypothetical protein LOC169436, MGC43306, Protein kinase like protein SgK071, SGK 071, SGK071, SGK71_HUMAN.
Background: C9orf96, also known as Protein kinase-like protein SgK071, is a 680 amino acid protein that belongs to the Ser/Thr protein kinase family of the protein kinase superfamily. There are three isoforms of C9orf96 that are produced as a result of alternative splicing events. The gene encoding C9orf96 maps to human chromosome 9, which 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.
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基因ID
- 169436
抗原
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