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NSDHL antibody

NSDHL Reactivity: Human, Rat WB, IF, IF (cc) Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6989853
  • Target See all NSDHL Antibodies
    NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))
    Reactivity
    • 18
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Rat
    Host
    • 14
    • 4
    Rabbit
    Clonality
    • 16
    • 2
    Polyclonal
    Conjugate
    • 14
    • 2
    • 1
    • 1
    This NSDHL antibody is un-conjugated
    Application
    • 14
    • 9
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF), Immunofluorescence (Cultured Cells) (IF (cc))
    Cross-Reactivity
    Human, Rat
    Purification
    Purified by Protein A.
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-240 of human NSDHL (NP_057006.1).
    Isotype
    IgG
    Top Product
    Discover our top product NSDHL Primary Antibody
  • Application Notes
    WB 1:300-5000
    IF(ICC) 1:50-200
    IF()
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C for 12 months.
    Expiry Date
    12 months
  • Target
    NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))
    Alternative Name
    NSDHL (NSDHL Products)
    Synonyms
    zgc:112474 antibody, H105E3 antibody, SDR31E1 antibody, XAP104 antibody, AI747449 antibody, Bpa antibody, Str antibody, NAD(P) dependent steroid dehydrogenase-like antibody, NAD(P) dependent steroid dehydrogenase-like L homeolog antibody, NSDHL antibody, nsdhl antibody, nsdhl.L antibody, Nsdhl antibody
    Background

    Synonyms: NSDHL,H105E3,SDR31E1,XAP104

    Background: The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene.

    Gene ID
    50814
    UniProt
    Q15738
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