RB12B抗体应用：WB 1:500-2000

RB22A抗体应用：WB 1:500-2000 ELISA 1:5000-20000RAB22A, member RAS oncogene family(RAB22A) Homo sapiens The protein encoded by this gene is a member of the RAB family of small GTPases. The GTP-bound form of the encoded protein has been shown to interact with early-endosomal antigen 1, and may be involved in the trafficking of and interaction between endosomal compartments. [provided by RefSeq, Jul 2008],

RB27A抗体应用：WB 1:500-2000 ELISA 1:5000-20000RAB27A, member RAS oncogene family(RAB27A) Homo sapiens The protein encoded by this gene belongs to the small GTPase superfamily, Rab family. The protein is membrane-bound and may be involved in protein transport and small GTPase mediated signal transduction. Mutations in this gene are associated with Griscelli syndrome type 2. Alternative splicing occurs at this locus and four transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008],

RB33B抗体应用：WB 1:500-2000 ELISA 1:5000-20000RAB33B, member RAS oncogene family(RAB33B) Homo sapiens This gene encodes a small GTP-binding protein of the Rab GTPase family, whose members function in vesicle transport during protein secretion and endocytosis. Rab GTPases are active, membrane-associated proteins that recruit effector proteins in the GTP-bound state and inactive cytosolic proteins when in a GDP-bound state. The protein encoded by this gene is ubiquitously expressed and has been implicated in Golgi to endoplasmic reticulum cycling of Golgi enzymes. In addition, this protein regulates Golgi homeostasis and coordinates intra-Golgi retrograde trafficking. Allelic variants in this gene have been associated with Dyggve-Melchior-Clausen syndrome and Smith-McCort dysplasia 2, which are autosomal recessive spondyloepimetaphyseal dysplasias characterized by skeletal abnormalities. [provided by RefSeq, Sep 2016],

RB39A抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:May be involved in vesicular trafficking.,similarity:Belongs to the small GTPase superfamily. Rab family.,

RB39B抗体应用：WB 1:500-2000 ELISA 1:5000-20000RAB39B, member RAS oncogene family(RAB39B) Homo sapiens This gene encodes a member of the Rab family of proteins. Rab proteins are small GTPases that are involved in vesicular trafficking. Mutations in this gene are associated with X-linked mental retardation. [provided by RefSeq, Aug 2013],

RB40A抗体应用：WB 1:500-2000 ELISA 1:5000-20000RAB40A, member RAS oncogene family(RAB40A) Homo sapiens This gene encodes a member of the Rab40 subfamily of Rab small GTP-binding proteins that contains a C-terminal suppressors of cytokine signaling box. [provided by RefSeq, Apr 2010],

RB40C抗体应用：WB 1:500-2000 ELISA 1:5000-20000domain:The SOCS box domain mediates the interaction with the Elongin BC complex, an adapter module in different E3 ubiquitin ligase complexes.,function:Probable substrate-recognition component of a SCF-like ECS (Elongin-Cullin-SOCS-box protein) E3 ubiquitin ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins.,pathway:Protein modification; protein ubiquitination.,similarity:Belongs to the small GTPase superfamily. Rab family.,similarity:Contains 1 SOCS box domain.,subunit:Component of the probable SCF-like ECS(RAB40C) E3 ubiquitin-protein ligase complex which contains CUL5, RNF7/RBX2, Elongin BC complex and RAB40C. Interacts with CUL5, RNF7, TCEB1 and TCEB2.,

RB40L抗体应用：WB 1:500-2000 ELISA 1:5000-20000RAB40A, member RAS oncogene family-like(RAB40AL) Homo sapiens This gene encodes a member of the Rab40 subfamily of Rab small GTP-binding proteins that contains a C-terminal suppressors of cytokine signaling box. Disruptions in this gene are associated with Duchenne muscular dystrophy. [provided by RefSeq, Apr 2010],

RB6I2抗体应用：WB 1:500-2000 ELISA 1:5000-20000ELKS/RAB6-interacting/CAST family member 1(ERC1) Homo sapiens The protein encoded by this gene is a member of a family of RIM-binding proteins. RIMs are active zone proteins that regulate neurotransmitter release. This gene has been found fused to the receptor-type tyrosine kinase gene RET by gene rearrangement due to the translocation t(10;12)(q11;p13) in thyroid papillary carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014],