FAM153B 抗体 (AA 301-387)
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- 抗原 See all FAM153B products
- FAM153B (Family with Sequence Similarity 153, Member B (FAM153B))
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抗原表位
- AA 301-387
- 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 FAM153B antibody is un-conjugated
- 应用范围
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM153B
- 亚型
- IgG
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anti-Family with Sequence Similarity 153, Member B (FAM153B) (AA 254-303) antibody
FAM153B 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 153, Member B (FAM153B) (AA 146-195) antibodyFAM153B 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 153, Member B (FAM153B) (C-Term) antibodyFAM153B 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
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
- FAM153B (Family with Sequence Similarity 153, Member B (FAM153B))
- 别名
- Fam153b (FAM153B 产品)
- 别名
- family with sequence similarity 153 member B antibody, FAM153B antibody
- 背景
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Synonyms: DKFZp434D115, F153B_HUMAN, FAM153B, Family with sequence similarity 153, member B, Hypothetical protein LOC202134, OTTHUMP00000223257, Protein FAM153B.
Background: FAM153A, FAM153B and FAM153C are 310, 387 and 144 amino acid proteins, respectively, that are encoded by a genes 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.
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