Rab 3 GAP p150 Polyclonal Antibody

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商品货号： PLA017792

适应性： 人,小鼠,大鼠,猴

￥600元

规格：

40μL 100μL 200μL

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MSDS

说明书

商品描述

基因名称： RAB3GAP2
蛋白名称： Rab3 GTPase-activating protein non-catalytic subunit
Human_gene_id： 25782
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=25782
Human_swiss_prot_no： Q9H2M9
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q9H2M9/entry
Mouse_gene_id： 98732
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=98732
Mouse_swiss_prot_no： Q8BMG7
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q8BMG7
Rat_gene_id： 289350
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=289350
Rat_swiss_prot_no： Q5U1Z0
Rat_swiss_link： http://www.uniprot.org/uniprot/Q5U1Z0
特异性： Rab 3 GAP p150 Polyclonal Antibody detects endogenous levels of Rab 3 GAP p150 protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： RAB3GAP2; KIAA0839; Rab3 GTPase-activating protein non-catalytic subunit; RGAP-iso; Rab3 GTPase-activating protein 150 kDa subunit; Rab3-GAP p150; Rab3-GAP150; Rab3-GAP regulatory subunit
实测条带： 156kD
功能： disease:Defects in RAB3GAP2 are the cause of Martsolf syndrome [MIM:212720]. Martsolf syndrome is characterized by congenital cataracts, mental retardation, and hypogonadism. Inheritance is autosomal recessive.,function:Regulatory subunit of a GTPase activating protein that has specificity for Rab3 subfamily (RAB3A, RAB3B, RAB3C and RAB3D). Rab3 proteins are involved in regulated exocytosis of neurotransmitters and hormones. Rab3 GTPase-activating complex specifically converts active Rab3-GTP to the inactive form Rab3-GDP. Required for normal eye and brain development. May participate in neurodevelopmental processes such as proliferation, migration and differentiation before synapse formation, and non-synaptic vesicular release of neurotransmitters.,similarity:Belongs to the Rab3-GAP regulatory subunit family.,subcellular location:In neurons, it is enriched in the synaptic soluble fraction.,subunit:The Rab3 GTPase-activating complex is a heterodimer composed of RAB3GAP and RAB3-GAP150. The Rab3 GTPase-activating complex interacts with DMXL2.,tissue specificity:Ubiquitous.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Cytoplasm. In neurons, it is enriched in the synaptic soluble fraction.
组织表达： Ubiquitous.
科研货号： PLA017792

Rab 3 GAP p150 Polyclonal Antibody

Catalog No PLA017792

Product information

基因名称： RAB3GAP2
蛋白名称： Rab3 GTPase-activating protein non-catalytic subunit
Human_gene_id： 25782
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=25782
Human_swiss_prot_no： Q9H2M9
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q9H2M9/entry
Mouse_gene_id： 98732
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=98732
Mouse_swiss_prot_no： Q8BMG7
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q8BMG7
Rat_gene_id： 289350
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=289350
Rat_swiss_prot_no： Q5U1Z0
Rat_swiss_link： http://www.uniprot.org/uniprot/Q5U1Z0
特异性： Rab 3 GAP p150 Polyclonal Antibody detects endogenous levels of Rab 3 GAP p150 protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： RAB3GAP2; KIAA0839; Rab3 GTPase-activating protein non-catalytic subunit; RGAP-iso; Rab3 GTPase-activating protein 150 kDa subunit; Rab3-GAP p150; Rab3-GAP150; Rab3-GAP regulatory subunit
实测条带： 156kD
功能： disease:Defects in RAB3GAP2 are the cause of Martsolf syndrome [MIM:212720]. Martsolf syndrome is characterized by congenital cataracts, mental retardation, and hypogonadism. Inheritance is autosomal recessive.,function:Regulatory subunit of a GTPase activating protein that has specificity for Rab3 subfamily (RAB3A, RAB3B, RAB3C and RAB3D). Rab3 proteins are involved in regulated exocytosis of neurotransmitters and hormones. Rab3 GTPase-activating complex specifically converts active Rab3-GTP to the inactive form Rab3-GDP. Required for normal eye and brain development. May participate in neurodevelopmental processes such as proliferation, migration and differentiation before synapse formation, and non-synaptic vesicular release of neurotransmitters.,similarity:Belongs to the Rab3-GAP regulatory subunit family.,subcellular location:In neurons, it is enriched in the synaptic soluble fraction.,subunit:The Rab3 GTPase-activating complex is a heterodimer composed of RAB3GAP and RAB3-GAP150. The Rab3 GTPase-activating complex interacts with DMXL2.,tissue specificity:Ubiquitous.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Cytoplasm. In neurons, it is enriched in the synaptic soluble fraction.
组织表达： Ubiquitous.
科研货号： PLA017792

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