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NIR1 antibody (AA 237-478)

PITPNM3 Reactivity: Human ELISA, WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2686942
$202.21
Plus shipping costs $45.00
100 μL
Shipping to: United States
Delivery in 11 to 21 Business Days
  • Target See all NIR1 (PITPNM3) Antibodies
    NIR1 (PITPNM3) (PITPNM Family Member 3 (PITPNM3))
    Binding Specificity
    • 8
    • 2
    • 1
    AA 237-478
    Reactivity
    Human
    Host
    • 7
    • 4
    Rabbit
    Clonality
    • 11
    Polyclonal
    Conjugate
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NIR1 antibody is un-conjugated
    Application
    • 8
    • 7
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    ELISA, Western Blotting (WB)
    Specificity
    Humand and predicted against mouse and rat.
    Purification
    Affinity purified
    Immunogen
    Rabbit polyclonal PITPNM3 (1) antibody was raised against a recombinate human PITPNM3 protein 237-478aa (BC128583).
  • 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
    NIR1 (PITPNM3) (PITPNM Family Member 3 (PITPNM3))
    Alternative Name
    PITPNM3 (PITPNM3 Products)
    Synonyms
    ACKR6, CORD5, NIR1, RDGBA3, A330068P14Rik, AI848332, Ackr6, Gm880, PITPNM family member 3, PITPNM3, Pitpnm3
    Background
    This gene encodes a member of a family of membrane-associated phosphatidylinositol transfer domain-containing proteins. The calcium-binding protein has phosphatidylinositol (PI) transfer activity and interacts with the protein tyrosine kinase PTK2B (also known as PYK2). The protein is homologous to a Drosophila protein that is implicated in the visual transduction pathway in flies. Mutations in this gene result in autosomal dominant cone dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]
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