ALS2 (NM_001135745) Human Recombinant Protein

CAT:
882-PH31205E1
Size:
50 µg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
ALS2 (NM_001135745) Human Recombinant Protein - image 1

ALS2 (NM_001135745) Human Recombinant Protein

  • Background:

    The protein encoded by this gene contains an ATS1/RCC1-like domain, a RhoGEF domain, and a vacuolar protein sorting 9 (VPS9) domain, all of which are guanine-nucleotide exchange factors that activate members of the Ras superfamily of GTPases. The protein functions as a guanine nucleotide exchange factor for the small GTPase RAB5. The protein localizes with RAB5 on early endosomal compartments, and functions as a modulator for endosomal dynamics. Mutations in this gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]
  • Synonyms:

    ALS2CR6; ALSJ; IAHSP; PLSJ
  • Gene ID:

    57679
  • UniProt:

    Q96Q42
  • Accession Number mRNA:

    NM_001135745
  • Chromosomal Location:

    2q33.1
  • Expression System:

    E. coli
  • Tag:

    N-His
  • Related Pathways:

    Amyotrophic lateral sclerosis (ALS)
  • Field of Research:

    Amyotrophic lateral sclerosis (ALS)
  • Concentration:

    >50 ug/mL as determined by microplate BCA method
  • Purity:

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

    Liquid
  • Buffer:

    50mM Tris, 8M Urea, pH8.0.
  • Function:

    Druggable Genome
  • Molecular Weight:

    42.4 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:

    ALS2
  • Species:

    Human
  • Protein ID:

    NP_001129217
  • Overview:

    Purified recombinant protein of Human amyotrophic lateral sclerosis 2 (juvenile) (ALS2), transcript variant 2, full length, with N-terminal HIS tag, expressed in E. coli, 50ug
  • Gene ID URL:

    https://www.ncbi.nlm.nih.gov/gene/57679
  • Uniprot URL:

    https://www.uniprot.org/uniprot/Q96Q42
  • Accession Number mRNA URL:

    https://www.ncbi.nlm.nih.gov/nuccore/NM_001135745
  • Protein ID Link:

    https://www.ncbi.nlm.nih.gov/nuccore/NP_001129217