ENTHD1 抗体 (FITC)
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- 抗原 See all ENTHD1 products
- ENTHD1 (ENTH Domain Containing 1 (ENTHD1))
- 适用
- 人, 小鼠, 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 ENTHD1 antibody is conjugated to FITC
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ENTHD1/Epsin2B
- 亚型
- IgG
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anti-ENTH Domain Containing 1 (ENTHD1) (C-Term) antibody
ENTHD1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-ENTH Domain Containing 1 (ENTHD1) (AA 169-198), (N-Term) antibodyENTHD1 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB27894 unconjugated
anti-ENTH Domain Containing 1 (ENTHD1) (AA 176-206), (N-Term) antibodyENTHD1 适用: 人 WB, FACS, EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 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
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- ENTHD1 (ENTH Domain Containing 1 (ENTHD1))
- 别名
- Epsin2B (ENTHD1 产品)
- 别名
- CACNA1I antibody, dJ370M22.3 antibody, ENTH domain containing 1 antibody, ENTHD1 antibody
- 背景
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Synonyms: CACNA1I, ENTD1_HUMAN, ENTH domain containing 1, ENTH domain-containing protein 1, ENTHD1, Epsin 2B, Epsin-2B, Gm1242, Gm86.
Background: The ENTHD1 gene is conserved in chimpanzee, dog, cow, mouse and rat, and maps to human chromosome 22q13.1. Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
- 基因ID
- 953
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