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Mouse Anti-VPS33B Recombinant Antibody (3E11) (CBMAB-V0044-YC)

Provided herein is a Mouse monoclonal antibody against Human VPS33B. The antibody can be used for immunoassay techniques, such as ELISA, WB.
See all VPS33B antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
3E11
Antibody Isotype
IgG2a, к
Application
ELISA, WB

Basic Information

Immunogen
VPS33B (NP_061138.2, aa 1-100) partial recombinant protein with GST tag. Immunogen sequence: MAFPHRPDAP ELPDFSMLKR LARDQLIYLL EQLPGKKDLF IEADLMSPLD RIANVSILKQ HEVDKLYKVE NKPALSSNEQ LCFLVRPRIK NMRYIASLVN
Specificity
Human
Antibody Isotype
IgG2a, к
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Storage
Store at 4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
vacuolar protein sorting 33 homolog B (yeast)
Introduction
VPS33B is a member of the Sec-1 domain family, and encodes the human ortholog of rat Vps33b which is homologous to the yeast class C Vps33 protein. The mammalian class C vacuolar protein sorting proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. Mutations in VPS33B are associated with arthrogryposis-renal dysfunction-cholestasis syndrome.
Entrez Gene ID
26276
UniProt ID
Q9H267
Alternative Names
VPS33B, Late Endosome And Lysosome Associated; Vacuolar Protein Sorting 33 Homolog B (Yeast); Vacuolar Protein Sorting 33B (Yeast Homolog); HVPS33B
Function
May play a role in vesicle-mediated protein trafficking to lysosomal compartments and in membrane docking/fusion reactions of late endosomes/lysosomes. Mediates phagolysosomal fusion in macrophages (PubMed:18474358).
Proposed to be involved in endosomal maturation implicating VIPAS39. In epithelial cells, the VPS33B:VIPAS39 complex may play a role in the apical recycling pathway and in the maintenance of the apical-basolateral polarity (PubMed:20190753).
Seems to be involved in the sorting of specific cargos from the trans-Golgi network to alpha-granule-destined multivesicular bodies (MVBs) promoting MVBs maturation in megakaryocytes (By similarity).
Biological Process
Biological Process collagen fibril organization Source:Ensembl
Biological Process collagen metabolic process Source:MGI1 Publication
Biological Process endosome organization Source:UniProtKB1 Publication
Biological Process intracellular protein transport Source:GO_Central1 Publication
Biological Process intracellular transport Source:ComplexPortal1 Publication
Biological Process lysosome localization Source:UniProtKB1 Publication
Biological Process megakaryocyte development Source:Ensembl
Biological Process melanosome localization Source:UniProtKB1 Publication
Biological Process membrane fusion Source:UniProtKB1 Publication
Biological Process peptidyl-lysine hydroxylation Source:MGI1 Publication
Biological Process phagosome-lysosome fusion Source:ComplexPortal1 Publication
Biological Process platelet alpha granule organization Source:UniProtKB1 Publication
Biological Process protein transport Source:UniProtKB1 Publication
Biological Process regulation of platelet aggregation Source:Ensembl
Biological Process vesicle-mediated transport Source:MGI1 Publication
Cellular Location
Late endosome membrane
Lysosome membrane
Early endosome
Cytoplasmic vesicle, clathrin-coated vesicle
Recycling endosome
Colocalizes in clusters with VIPAS39 at cytoplasmic organelles (PubMed:19109425).
Colocalizes with RAB11A and VIPAS39 on recycling endosomes (PubMed:22753090).
Colocalizes with AP-3, clathrin, Rab5 and Rab7b (PubMed:21411634).
Colocalizes with M.tuberculosis PtpA in the cytosol of tuberculosis-infected macrophages and associates with phagosomes (PubMed:18474358).
Involvement in disease
Arthrogryposis, renal dysfunction and cholestasis syndrome 1 (ARCS1):
A multisystem disorder, characterized by neurogenic arthrogryposis multiplex congenita, renal tubular dysfunction and neonatal cholestasis with bile duct hypoplasia and low gamma glutamyl transpeptidase activity. Platelet dysfunction is common.
PTM
Phosphorylated on tyrosine residues.
(Microbial infection) Dephosphorylated by M.tuberculosis PtpA, which induces the reduction of host phagolysosome fusion in M.tuberculosis-infected macrophages.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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