C9orf41 抗体 (AA 101-200) (Cy5)
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- 抗原 See all C9orf41 products
- C9orf41 (Chromosome 9 Open Reading Frame 41 (C9orf41))
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抗原表位
- AA 101-200
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适用
- 大鼠, 小鼠
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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 C9orf41 antibody is conjugated to Cy5
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应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠, 大鼠
- 预测反应
- Human,Cow,Sheep,Pig,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C9orf41
- 亚型
- IgG
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anti-Chromosome 9 Open Reading Frame 41 (C9orf41) antibody
C9orf41 适用: 人 WB, FACS, IF, IHC (p), IHC 宿主: 小鼠 Monoclonal 6E4 unconjugated
anti-Chromosome 9 Open Reading Frame 41 (C9orf41) antibodyC9orf41 适用: 大鼠, 人, 犬, 猴 WB, FACS 宿主: 小鼠 Monoclonal 4A2 unconjugated
anti-Chromosome 9 Open Reading Frame 41 (C9orf41) antibodyC9orf41 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 41 (C9orf41) antibodyC9orf41 适用: 人 WB, FACS, IF 宿主: 小鼠 Monoclonal 1E8 unconjugated
anti-Chromosome 9 Open Reading Frame 41 (C9orf41) (AA 142-191) antibodyC9orf41 适用: 人, Cow, 马, 兔, Pig WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- C9orf41 (Chromosome 9 Open Reading Frame 41 (C9orf41))
- 别名
- C9orf41 (C9orf41 产品)
- 别名
- C9orf41 antibody, MGC115667 antibody, carnosine N-methyltransferase 1 antibody, carnosine N-methyltransferase 1 S homeolog antibody, CARNMT1 antibody, carnmt1.S antibody, carnmt1 antibody, Carnmt1 antibody
- 背景
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Synonyms: C9orf41, CI041_HUMAN, FLJ25795, UPF0586 protein C9orf41.
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 C9orf41 gene product has been provisionally designated C9orf41 pending further characterization.
- 基因ID
- 138199
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