C9orf96 抗体 (AA 101-200) (Biotin)
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- 抗原 See all C9orf96 products
- C9orf96 (Chromosome 9 Open Reading Frame 96 (C9orf96))
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抗原表位
- AA 101-200
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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 C9orf96 antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C9orf96
- 亚型
- IgG
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- 应用备注
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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
- C9orf96 (Chromosome 9 Open Reading Frame 96 (C9orf96))
- 别名
- C9orf96 (C9orf96 产品)
- 别名
- sk521 antibody, SgK071 antibody, Sk521 antibody, Sgk071 antibody, serine/threonine kinase like domain containing 1 antibody, serine/threonine kinase-like domain containing 1 L homeolog antibody, serine/threonine kinase-like domain containing 1 antibody, STKLD1 antibody, stkld1.L antibody, Stkld1 antibody
- 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.
- 基因ID
- 169436
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