RPP25L 抗体 (AA 1-100) (Biotin)
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- 抗原 See all RPP25L 抗体
- RPP25L (Ribonuclease P/MRP 25 Subunit-Like (RPP25L))
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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 RPP25L antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Mouse,Rat,Dog,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C9orf23
- 亚型
- IgG
- Top Product
- Discover our top product RPP25L Primary Antibody
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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
- RPP25L (Ribonuclease P/MRP 25 Subunit-Like (RPP25L))
- 别名
- C9orf23 (RPP25L 产品)
- 别名
- C9orf23 antibody, bA296L22.5 antibody, 2810432D09Rik antibody, AW987258 antibody, Rppl25 antibody, C8H9orf23 antibody, C9ORF23 antibody, CZH9orf23 antibody, RGD1306576 antibody, c9orf23 antibody, zgc:92794 antibody, ribonuclease P/MRP subunit p25 like antibody, ribonuclease P/MRP 25 subunit-like antibody, ribonuclease P/MRP 25kDa subunit-like antibody, RPP25L antibody, Rpp25l antibody, rpp25l antibody
- 背景
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Synonyms: Alba like protein C9orf23, bA296L22.5, C9orf23, MGC29635, Ribonuclease P protein subunit p25 like protein, Ribonuclease P/MRP 25 kDa subunit like, RNase P protein subunit like p25, Rpp25 like protein, RPP25L, RP25L_HUMAN.
Background: C9orf23 (chromosome 9 open reading frame 23) is a 163 amino acid protein that belongs to the histone-like Alba family and is encoded by a gene that maps to human chromosome 9p13.3. 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
- 138716
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