VAT1L 抗体 (AA 321-419)
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北京 101111
Quick Overview for VAT1L 抗体 (AA 321-419) (ABIN1386227)
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 321-419
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交叉反应
- 大鼠
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预测反应
- Human,Mouse,Dog,Cow,Pig
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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 VAT1L/KIAA1576
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亚型
- IgG
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anti-Vesicle Amine Transport 1-Like (VAT1L) (AA 1-419) antibody
VAT1L 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Vesicle Amine Transport 1-Like (VAT1L) (AA 1-419) antibodyVAT1L 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Vesicle Amine Transport 1-Like (VAT1L) (AA 80-129) antibodyVAT1L 适用: 人, 大鼠, 小鼠, 犬, 豚鼠, 兔, 斑马鱼, 马, Pig, Bat, 小鸡, 猴, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
anti-Vesicle Amine Transport 1-Like (VAT1L) (AA 391-419), (C-Term) antibodyVAT1L 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB31950 unconjugated
anti-Vesicle Amine Transport 1-Like (VAT1L) (N-Term) antibodyVAT1L 适用: 人, 大鼠, 小鼠, 犬, 豚鼠, 兔, 斑马鱼, Cow, 马 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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- VAT1L (Vesicle Amine Transport 1-Like (VAT1L))
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别名
- VAT1L/KIAA1576
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背景
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Synonyms: Probable oxidoreductase KIAA1576, Synaptic vesicle membrane protein VAT 1 homolog like, Synaptic vesicle membrane protein VAT-1 homolog-like, VAT 1L, VAT1L, VAT1L_HUMAN, Vesicle amine transport protein 1 homolog T. calornica like.
Background: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.
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基因ID
- 3384
抗原
-
