FAM13B 抗体
This anti-FAM13B antibody is a 兔 多克隆 antibody detecting FAM13B in ELISA 和 IHC. Suitable for 人 和 小鼠.
Quick Overview for FAM13B 抗体 (ABIN7243301)
抗原
FAM13B
(Family with Sequence Similarity 13, Member B (FAM13B))
适用
人, 小鼠
宿主
兔
克隆类型
多克隆
标记
This FAM13B antibody is un-conjugated
应用范围
ELISA, Immunohistochemistry (IHC)
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Synthetic peptide of human FAM13B
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亚型
- IgG
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anti-Family with Sequence Similarity 13, Member B (FAM13B) (AA 1-915) antibody
FAM13B 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- IHC 1:50-1:200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.4 mg/mL
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缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))
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别名
- FAM13B
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背景
- FAM13B is a 915 amino acid protein that is encoded by a gene that maps 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.
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NCBI登录号
- NP_057687
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UniProt
- Q9NYF5
抗原
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