SLC25A20 monoclonal antibody (M02), clone M2

Catalog # H00000788-M02

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Size:100 ug
Price: USD $ 335.00
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  • +1-909-264-1399
    +1-909-992-0619
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Images
Immunofluorescence
Application

Immunofluorescence

Immunofluorescence of monoclonal antibody to SLC25A20 on HeLa cell . [antibody concentration 10 ug/ml]

  • Specification

    Product Description

    Mouse monoclonal antibody raised against a full-length recombinant SLC25A20.

    Immunogen

    SLC25A20 (AAH01689, 1 a.a. ~ 301 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    MADQPKPISPLKNLLAGGFGGVCLVFAGHPLDTVKVRLQTQPPSLPGQPPMYSGTFDCFRKTLFREGITGLYRGMAAPIIGVTPMFAVCFFGFGLGKKLQQKHPEDVLSYPQLFAAGMLSGVFTTGIMTPGERIKCLLQIQASSGESKYTGTLDCAKKLYQEFGIRGIYKGTVLTLMRDVPASGMYFMTYEWLKNIFTPEGKRVSELSAPRILVAGGIAGIFNWAVAIPPDVLKSRFQTAPPGKYPNGFRDVLRELIRDEGVTSLYKGFNAVMIRAFPANAACFLGFEVAMKFLNWATPNL

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (93); Rat (91)

    Isotype

    IgG1 kappa

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    ELISA

    Immunofluorescence

    Immunofluorescence of monoclonal antibody to SLC25A20 on HeLa cell . [antibody concentration 10 ug/ml]
  • Gene Info — SLC25A20

    Entrez GeneID

    788

    GeneBank Accession#

    BC001689

    Protein Accession#

    AAH01689

    Gene Name

    SLC25A20

    Gene Alias

    CAC, CACT

    Gene Description

    solute carrier family 25 (carnitine/acylcarnitine translocase), member 20

    Omim ID

    212138

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. [provided by RefSeq

    Other Designations

    carnitine/acylcarnitine carrier protein|carnitine/acylcarnitine translocase

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