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上海允麥生物科技有限公司
中級(jí)會(huì)員·7年
- 聯(lián)系人：
- 麥經(jīng)理
- 電話：
- 86-021-34553900
- 手機(jī)：
- 15121004110
- 傳真：
- 86-021-34553900
- 地址：
- 上海市青浦區(qū)
- 個(gè)性化：
- www.shymbio.com
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- www.shymbio.com
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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(lái)源：Recombinant Human
純度：≥95% SDS-PAGE
表達(dá)系統(tǒng)：Escherichia coli
標(biāo)簽：His tag
蛋白長(zhǎng)度：Full length protein
內(nèi)毒素水平：<1.000 Eu/µg
純化方法：HPLC
應(yīng)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(lái)源：Rabbit
克隆類型：Polyclonal
濃度：1mg/ml
亞型：IgG
應(yīng)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(yīng)：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年
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(lái)源：Mouse
克隆類型：Monoclonal
濃度：1mg/ml
亞型：IgG
應(yīng)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(yīng): 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.
