SLC27A2 (Human) Recombinant Protein (Q01)

Catalog # H00011001-Q01

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Size:25 ug
Price: USD $ 510.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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  • Specification

    Product Description

    Human SLC27A2 partial ORF ( NP_003636, 25 a.a. - 123 a.a.) recombinant protein with GST-tag at N-terminal.

    Sequence

    YFFQDIGYFLKVAAVGRRVRSYGQRRPARTILRAFLEKARQTPHKPFLLFRDETLTYAQVDRRSNQVARALHDHLGLRQGDCVALLMGNEPAYVWLWLG

    Host

    Wheat Germ (in vitro)

    Theoretical MW (kDa)

    36.63

    Interspecies Antigen Sequence

    Mouse (76); Rat (76)

    Preparation Method

    in vitro wheat germ expression system

    Purification

    Glutathione Sepharose 4 Fast Flow

    Quality Control Testing

    12.5% SDS-PAGE Stained with Coomassie Blue.

    Storage Buffer

    50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

    Note

    Best use within three months from the date of receipt of this protein.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

    Western Blot (Recombinant protein)

    Antibody Production

    Protein Array

  • Gene Info — SLC27A2

    Entrez GeneID

    11001

    GeneBank Accession#

    NM_003645

    Protein Accession#

    NP_003636

    Gene Name

    SLC27A2

    Gene Alias

    ACSVL1, FACVL1, FATP2, HsT17226, VLACS, VLCS, hFACVL1

    Gene Description

    solute carrier family 27 (fatty acid transporter), member 2

    Omim ID

    603247

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq

    Other Designations

    very long-chain fatty-acid-coenzyme A ligase 1|very-long-chain acyl-CoA synthetase

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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