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中級會員·7年
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VAT1抗原,嗜鉻顆粒胺轉(zhuǎn)運蛋白VAT1抗原

2024-12-4  閱讀(155)

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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    

濃度:1mg/ ml

來源:Recombinant Human

純度:≥95% SDS-PAGE

表達系統(tǒng):Escherichia coli

標簽:His tag  

蛋白長度:Full length protein

內(nèi)毒素水平:<1.000 Eu/µg

純化方法:HPLC

應用:SDS-PAGE,Western blot,ELISA

Biological activity,immunology research

保存:-20℃

保質(zhì)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.



產(chǎn)品名稱:Rabbit Anti-VAT1  antibody

Rabbit Anti-VAT1  

別名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

來源:Rabbit

克隆類型:Polyclonal

濃度:1mg/ml

亞型:IgG

應用: 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

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

理論分子量:44kDa

免疫原:KLH conjugated synthetic peptide derived from human VAT1

保存:-20
保質(zhì)期:1

 

單克隆抗體

產(chǎn)品名稱:Anti-VAT1 antibody

Mouse Anti-VAT1 

別名: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

來源:Mouse

克隆類型:Monoclonal

濃度:1mg/ml

亞型:IgG

應用: 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

反應: Human

理論分子量:44kDa

免疫原:KLH conjugated synthetic peptide derived from human VAT1

保存:-20
保質(zhì)期:1

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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