SAMD14 抗体 (AA 231-330)
Quick Overview for SAMD14 抗体 (AA 231-330) (ABIN718346)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 231-330
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预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Rabbit
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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 SAMD14
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亚型
- IgG
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anti-Sterile alpha Motif Domain Containing 14 (SAMD14) (AA 31-80) antibody
SAMD14 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 马, 兔, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Sterile alpha Motif Domain Containing 14 (SAMD14) (N-Term) antibodySAMD14 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Sterile alpha Motif Domain Containing 14 (SAMD14) (N-Term) antibodySAMD14 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 马, 兔 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
ICC 1:100-500 -
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- SAMD14 (Sterile alpha Motif Domain Containing 14 (SAMD14))
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别名
- SAMD14
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背景
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Synonyms: Sterile alpha motif domain-containing protein 14, SAM domain-containing protein 14, SAMD14
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 eukaryotes. The SAM domain is known to bind RNA and is arranged in a small five-helix bundle with two large interfaces. SAMD14 (sterile alpha motif domain-containing protein 14) is a 417 amino acid protein encoded by the SAMD14 gene which maps to human chromosome 17. Chromosome 17 makes up over 2.5 % of the human genome with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Chromosome 17 is also linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth, Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease.
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基因ID
- 201191
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UniProt
- Q8IZD0
抗原
-
