C5orf35 抗体 (AA 1-100) (Biotin)
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- 抗原 See all C5orf35 products
- C5orf35 (Chromosome 5 Open Reading Frame 35 (C5orf35))
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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 C5orf35 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Dog
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C5orf35
- 亚型
- IgG
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anti-Chromosome 5 Open Reading Frame 35 (C5orf35) (AA 1-299) antibody
C5orf35 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 5 Open Reading Frame 35 (C5orf35) (AA 71-120) antibodyC5orf35 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 5 Open Reading Frame 35 (C5orf35) (N-Term) antibodyC5orf35 适用: 人 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
- C5orf35 (Chromosome 5 Open Reading Frame 35 (C5orf35))
- 别名
- C5orf35 (C5orf35 产品)
- 别名
- DKFZp468C1120 antibody, C5orf35 antibody, SET domain containing 9 antibody, SETD9 antibody, setd9 antibody
- 背景
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Synonyms: C5orf35 chromosome 5 open reading frame 35, Chromosome 5 open reading frame 35, Hypothetical protein LOC133383, MGC33648, Uncharacterized protein C5orf35, SET domain-containing protein 9, SETD9_HUMAN.
Background: C5orf35 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf35 gene product has been provisionally designated C5orf35 pending further characterization.
- 基因ID
- 133383
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