CCDC125 抗体 (AA 151-250)
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- 抗原 See all CCDC125 抗体
- CCDC125 (Coiled-Coil Domain Containing 125 (CCDC125))
- 抗原表位
- AA 151-250
- 适用
- 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 CCDC125 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Cow,Sheep,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CCDC125
- 亚型
- IgG
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- CCDC125 (Coiled-Coil Domain Containing 125 (CCDC125))
- 别名
- CCDC125 (CCDC125 产品)
- 别名
- KENAE antibody, 5830436D01Rik antibody, AL023012 antibody, Kenae-like antibody, RGD1561673 antibody, si:ch211-214j8.8 antibody, coiled-coil domain containing 125 antibody, CCDC125 antibody, Ccdc125 antibody, ccdc125 antibody
- 背景
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Synonyms: CC125_HUMAN, CCDC125, Coiled-coil domain-containing protein 125, KENAE,y Protein kenae.
Background: CCDC125, also known as KENAE, is a 511 amino acid protein expressed as two isoforms produced by alternative splicing and encoded by a gene mapping to human chromosome 5. 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.
- 基因ID
- 202243
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