TSPYL1 抗体 (C-Term)
(5 references)Quick Overview for TSPYL1 抗体 (C-Term) (ABIN1881952)
抗原
See all TSPYL1 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 343-372, C-Term
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预测反应
- M
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纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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免疫原
- This TSPYL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 343-372 amino acids from the C-terminal region of human TSPYL1.
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亚型
- Ig Fraction
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anti-TSPY-Like 1 (TSPYL1) (AA 1-100) antibody
TSPYL1 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 4F11 unconjugated
anti-TSPY-Like 1 (TSPYL1) antibodyTSPYL1 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-TSPY-Like 1 (TSPYL1) (AA 1-438) antibodyTSPYL1 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-TSPY-Like 1 (TSPYL1) antibodyTSPYL1 适用: 人, 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 1:1000
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: 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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有效期
- 6 months
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: "Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility." in: Fertility and sterility, Vol. 92, Issue 4, pp. 1347-50, (2009) (PubMed).
: "Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster." in: Blood cells, molecules & diseases, Vol. 37, Issue 2, pp. 82-90, (2006) (PubMed).
: "Genetic investigation of the TSPYL1 gene in sudden infant death syndrome." in: Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 8, Issue 1, pp. 55-8, (2006) (PubMed).
: "Identification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags." in: Biochemical and biophysical research communications, Vol. 345, Issue 3, pp. 1022-32, (2006) (PubMed).
: "Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 101, Issue 32, pp. 11689-94, (2004) (PubMed).
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: "Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility." in: Fertility and sterility, Vol. 92, Issue 4, pp. 1347-50, (2009) (PubMed).
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- TSPYL1 (TSPY-Like 1 (TSPYL1))
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别名
- TSPYL1
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背景
- The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT).
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分子量
- 49192
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NCBI登录号
- NP_003300
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UniProt
- Q9H0U9
抗原
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