GAPT 抗体 (AA 21-120)
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- 抗原 See all GAPT 抗体
- GAPT (GRB2-Binding Adaptor Protein, Transmembrane (GAPT))
- 抗原表位
- AA 21-120
- 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 GAPT antibody is un-conjugated
- 应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GAPT
- 亚型
- IgG
- Top Product
- Discover our top product GAPT Primary Antibody
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anti-GRB2-Binding Adaptor Protein, Transmembrane (GAPT) (AA 84-112) antibody
GAPT 适用: 人 WB 宿主: 兔 Polyclonal RB40905 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
ICC 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
- 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
- GAPT (GRB2-Binding Adaptor Protein, Transmembrane (GAPT))
- 别名
- GAPT (GAPT 产品)
- 别名
- C5orf29 antibody, 9830130M13Rik antibody, GRB2 binding adaptor protein, transmembrane antibody, Grb2-binding adaptor, transmembrane antibody, GAPT antibody, Gapt antibody
- 背景
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Synonyms: C5orf29, Gapt, GAPT_HUMAN, Grb2-binding adaptor transmembrane, Growth factor receptor-bound protein 2-binding adapter protein, Growth factor receptor-bound protein 2-binding adapter protein, transmembrane, Protein GAPT, transmembrane.
Background: 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 C5orf29 gene product has been provisionally designated C5orf29 pending further characterization.
- 基因ID
- 202309
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