Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

L2HGDH antibody

L2HGDH Reactivity: Human, Mouse WB, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6293250
  • Target See all L2HGDH Antibodies
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Reactivity
    • 31
    • 15
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 36
    Rabbit
    Clonality
    • 36
    Polyclonal
    Conjugate
    • 18
    • 6
    • 4
    • 4
    • 2
    • 2
    This L2HGDH antibody is un-conjugated
    Application
    • 26
    • 25
    • 9
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human L2HGDH
    Isotype
    IgG
    Top Product
    Discover our top product L2HGDH Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    IF 1:50 - 1:200
    Comment

    Widely expressed, Highly expressed in brain, testis and muscle, Expressed to a lower extent in lymphocytes, fibroblasts, keratinocytes, placenta, bladder, small intestine, liver and bone marrow

    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20C. Avoid freeze / thaw cycles.
  • Target
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Alternative Name
    L2HGDH (L2HGDH Products)
    Synonyms
    RGD1306250 antibody, C14orf160 antibody, BC016226 antibody, L-2-hydroxyglutarate dehydrogenase antibody, L2hgdh antibody, L2HGDH antibody
    Background
    This gene encodes L-2-hydroxyglutarate dehydrogenase, a FAD-dependent enzyme that oxidizes L-2-hydroxyglutarate to alpha-ketoglutarate in a variety of mammalian tissues. Mutations in this gene cause L-2-hydroxyglutaric aciduria, a rare autosomal recessive neurometabolic disorder resulting in moderate to severe mental retardation.
    Molecular Weight
    50.316 kDa
    Gene ID
    79944
    UniProt
    Q9H9P8
You are here:
Support