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PITPNM Family Member 3 (PITPNM3) antibody Primary Antibody

PITPNM3 Reactivity: Human, Mouse, Rat IF (p), IHC (p), WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1387251
$339.90
Plus shipping costs $45.00
100 μL
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  • Target
    PITPNM Family Member 3 (PITPNM3)
    Reactivity
    Human, Mouse, Rat
    Host
    • 7
    • 4
    Rabbit
    Clonality
    • 11
    Polyclonal
    Conjugate
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Un-conjugated
    Application
    • 8
    • 7
    • 4
    • 2
    • 1
    Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human NIR1/RDGBA3
    Isotype
    IgG
  • Application Notes
    WB 1:100-1000
    IHC-P 1:100-500
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.
    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 -20°C
    Expiry Date
    12 months
  • Target
    PITPNM Family Member 3 (PITPNM3)
    Alternative Name
    NIR1 (PITPNM3 Antibody Abstract)
    Synonyms
    ACKR6, CORD5, NIR1, RDGBA3, A330068P14Rik, AI848332, Ackr6, Gm880, PITPNM family member 3, PITPNM3, Pitpnm3
    Background

    Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro) (By similarity). Binds calcium ions.Involvement in disease:Defects in PITPNM3 are the cause of cone-rod dystrophy type 5 (CORD5) . CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration.

    Synonyms: membrane-associated 3, CORD5, Membrane associated phosphatidylinositol transfer protein 3, Membrane-associated phosphatidylinositol transfer protein 3, NIR 1, NIR-1, NIR1, Phosphatidylinositol transfer protein, Phosphatidylinositol transfer protein, membrane-associated 3, PITM3_HUMAN, PITPnm 3, PITPNM, PITPNM family member 3, Pitpnm3, PYK2 N terminal domain interacting receptor 1, PYK2 N-terminal domain-interacting receptor 1, RDGBA3, retinal degeneration B alpha 3.

    Gene ID
    83394
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