Recombinant human VAT1   

VAT1 antibody,FLJ20230 antibody,Membrane protein of cholinergic synaptic vesicles antibody,MGC124668 antibody,OTTMUSP00000002784 antibody,RP23-328K2.5 antibody,Synaptic vesicle membrane protein VAT 1 homolog antibody,Synaptic vesicle membrane protein VAT-1 homolog antibody,VAT 1 antibody,VAT1 antibody,VAT1_HUMAN antibody,VATI antibody,Vesicle amine transport protein 1 antibody,Vesicle amine transport protein 1 homolog (T. californica) antibody    

浓度：1mg/ ml

来源：Recombinant Human

纯度：≥95% SDS-PAGE

表达系统：Escherichia coli

标签：His tag  

蛋白长度：Full length protein

内毒素水平：<1.000 Eu/µg

纯化方法：HPLC

应用：SDS-PAGE，Western blot，ELISA

Biological activity,immunology research

保存：-20℃

保质期：1年

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.

产品名称：Rabbit Anti-VAT1  antibody

Rabbit Anti-VAT1  

别名：VAT1 antibody,FLJ20230 antibody,Membrane protein of cholinergic synaptic vesicles antibody,MGC124668 antibody,OTTMUSP00000002784 antibody,RP23-328K2.5 antibody,Synaptic vesicle membrane protein VAT 1 homolog antibody,Synaptic vesicle membrane protein VAT-1 homolog antibody,VAT 1 antibody,VAT1 antibody,VAT1_HUMAN antibody,VATI antibody,Vesicle amine transport protein 1 antibody,Vesicle amine transport protein 1 homolog (T. californica) antibody

来源：Rabbit

克隆类型：Polyclonal

浓度：1mg/ml

亚型：IgG

应用： WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500

反应：Mouse,Rat (predicted: Human,Pig,Sheep,Chicken,Dog,Horse)

理论分子量：44kDa

免疫原：KLH conjugated synthetic peptide derived from human VAT1

保存：-20℃
保质期：1年

单克隆抗体

产品名称：Anti-VAT1 antibody

Mouse Anti-VAT1 

别名：VAT1 antibody,FLJ20230 antibody,Membrane protein of cholinergic synaptic vesicles antibody,MGC124668 antibody,OTTMUSP00000002784 antibody,RP23-328K2.5 antibody,Synaptic vesicle membrane protein VAT 1 homolog antibody,Synaptic vesicle membrane protein VAT-1 homolog antibody,VAT 1 antibody,VAT1 antibody,VAT1_HUMAN antibody,VATI antibody,Vesicle amine transport protein 1 antibody,Vesicle amine transport protein 1 homolog (T. californica) antibody

来源：Mouse

克隆类型：Monoclonal

浓度：1mg/ml

亚型：IgG

应用： WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500

反应: Human

理论分子量：44kDa

免疫原：KLH conjugated synthetic peptide derived from human VAT1

保存：-20℃
保质期：1年

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.