SAMD7 抗体 (Biotin)
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北京 101111
Quick Overview for SAMD7 抗体 (Biotin) (ABIN1400275)
抗原
适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human SAMD7
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亚型
- IgG
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anti-Sterile alpha Motif Domain Containing 7 (SAMD7) (AA 1-300) antibody
SAMD7 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Sterile alpha Motif Domain Containing 7 (SAMD7) (AA 175-224) antibodySAMD7 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Sterile alpha Motif Domain Containing 7 (SAMD7) (AA 202-230) antibodySAMD7 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB29437 unconjugated
anti-Sterile alpha Motif Domain Containing 7 (SAMD7) (AA 209-238), (Middle Region) antibodySAMD7 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
- IHC-P 1:200-400
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: 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 for 12 months.
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有效期
- 12 months
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- SAMD7 (Sterile alpha Motif Domain Containing 7 (SAMD7))
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别名
- SAMD7
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背景
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Synonyms: SAM domain-containing protein 7, Samd7, Samd 7, Samd-7, SAMD7_HUMAN, sterile alpha mot domain containing 7, Sterile alpha mot domain-containing protein 7.
Background: The sterile alpha motif (SAM) domain is a 70 residue structure found in a large number of proteins involved in diverse processes present throughout the eukaryotes. The SAM domain is known to bind RNA and is arranged in a small five-helix bundle with two large interfaces. SAMD7 (Sterile alpha motif domain-containing protein 7), is a 446 amino acid protein encoded by the SAMD7 gene which maps to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
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基因ID
- 344658
抗原
-
