C5orf24 抗体 (AA 51-150) (Biotin)
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- 抗原 See all C5orf24 products
- C5orf24 (Chromosome 5 Open Reading Frame 24 (C5orf24))
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抗原表位
- AA 51-150
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适用
- 大鼠
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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 C5orf24 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))
- 交叉反应
- 大鼠
- 预测反应
- Human,Mouse,Cow,Pig,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C5orf24
- 亚型
- IgG
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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
- C5orf24 (Chromosome 5 Open Reading Frame 24 (C5orf24))
- 别名
- C5orf24 (C5orf24 产品)
- 别名
- C5orf24 antibody, MGC84502 antibody, MGC121760 antibody, MGC146478 antibody, AA119856 antibody, D530037I19Rik antibody, chromosome 5 open reading frame 24 antibody, chromosome 13 C5orf24 homolog antibody, chromosome 5 open reading frame 24 L homeolog antibody, chromosome 6 open reading frame, human C5orf24 antibody, chromosome 5 open reading frame, human C5orf24 antibody, chromosome 7 open reading frame, human C5orf24 antibody, RIKEN cDNA B230219D22 gene antibody, C5orf24 antibody, C13H5orf24 antibody, c5orf24.L antibody, C6H5orf24 antibody, c5orf24 antibody, C5H5orf24 antibody, C7H5orf24 antibody, B230219D22Rik antibody
- 背景
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Synonyms: Chromosome 5 open reading frame 24, FLJ37562, Hypothetical protein LOC134553.
Background: C5orf24 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 C5orf24 gene product has been provisionally designated C5orf24 pending further characterization.
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