VPS13B (NM_181661) Human Recombinant Protein

• Background:

  This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

• Synonyms:

  CHS1; COH1

• Gene ID:

  157680

• UniProt:

  Q7Z7G8

• Accession Number mRNA:

  NM_181661

• Chromosomal Location:

  8q22.2

• Expression System:

  HEK293T

• Tag:

  C-Myc/DDK

• Concentration:

  >50 ug/mL as determined by microplate BCA method

• Purity:

  > 80% as determined by SDS-PAGE and Coomassie blue staining

• Form:

  Liquid

• Buffer:

  25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

• Molecular Weight:

  47 kDa

• Storage Conditions:

  Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.

• Symbol:

  VPS13B

• Species:

  Human

• Protein ID:

  NP_858047

• Overview:

  Recombinant protein of human vacuolar protein sorting 13 homolog B (yeast) (VPS13B), transcript variant 4

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/157680

• Uniprot URL:

  https://www.uniprot.org/uniprot/Q7Z7G8

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_181661

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_858047