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FVT1 antibody (AA 63-218)

KDSR Reactivity: Human ELISA, WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2686701
$202.21
Plus shipping costs $45.00
100 μL
Shipping to: United States
Delivery in 11 to 21 Business Days
  • Target See all FVT1 (KDSR) Antibodies
    FVT1 (KDSR) (3-Ketodihydrosphingosine Reductase (KDSR))
    Binding Specificity
    • 15
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 63-218
    Reactivity
    • 29
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 27
    • 3
    Rabbit
    Clonality
    • 27
    • 3
    Polyclonal
    Conjugate
    • 11
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FVT1 antibody is un-conjugated
    Application
    • 13
    • 13
    • 12
    • 6
    • 6
    • 5
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    ELISA, Western Blotting (WB)
    Purification
    Affinity purified
    Immunogen
    Rabbit polyclonal KDSR(1)antibody was raised against a recombinate human KDSR protein 63-218aa(BC008797).
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    PBS, pH 7.4 with 0.02 % sodium azide.
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C,-20 °C
  • Target
    FVT1 (KDSR) (3-Ketodihydrosphingosine Reductase (KDSR))
    Alternative Name
    KDSR (KDSR Products)
    Synonyms
    fvt1, zgc:55947, FVT1, DHSR, SDR35C1, 6330410P18Rik, 9430079B08Rik, Fvt1, 3-ketodihydrosphingosine reductase, kdsr, KDSR, Kdsr
    Background
    This gene catalyzes the reduction of 3-ketodihydrosphingosine to dihydrosphingosine. The putative active site residues of the encoded protein are found on the cytosolic side of the endoplasmic reticulum membrane. A chromosomal rearrangement involving this gene is a cause of follicular lymphoma, also known as type II chronic lymphatic leukemia. The mutation of a conserved residue in the bovine ortholog causes spinal muscular atrophy. [provided by RefSeq, Jul 2008]
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