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RIN2 antibody

RIN2 Reactivity: Human, Mouse WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6290905
  • Target See all RIN2 Antibodies
    RIN2 (Ras and Rab Interactor 2 (RIN2))
    Reactivity
    • 9
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Human, Mouse
    Host
    • 5
    • 4
    Rabbit
    Clonality
    • 6
    • 3
    Polyclonal
    Conjugate
    • 9
    This RIN2 antibody is un-conjugated
    Application
    • 9
    • 5
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human RIN2
    Isotype
    IgG
    Top Product
    Discover our top product RIN2 Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    Comment

    Widely expressed, Expressed in heart, kidney, lung placenta, Expressed at low level in skeletal muscle, spleen and peripheral blood

    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
    RIN2 (Ras and Rab Interactor 2 (RIN2))
    Alternative Name
    RIN2 (RIN2 Products)
    Synonyms
    RIN2 antibody, RINL antibody, rassf4 antibody, MACS antibody, RASSF4 antibody, 2010003K16Rik antibody, 4632403N06Rik antibody, AW821980 antibody, Ras and Rab interactor 2 antibody, Rin2 antibody, RIN2 antibody, rin2 antibody
    Background
    The RAB5 protein is a small GTPase involved in membrane trafficking in the early endocytic pathway. The protein encoded by this gene binds the GTP-bound form of the RAB5 protein preferentially over the GDP-bound form, and functions as a guanine nucleotide exchange factor for RAB5. The encoded protein is found primarily as a tetramer in the cytoplasm and does not bind other members of the RAB family. Mutations in this gene cause macrocephaly alopecia cutis laxa and scoliosis (MACS) syndrome, an elastic tissue disorder, as well as the related connective tissue disorder, RIN2 syndrome. Alternative splicing results in multiple transcript variants.
    Molecular Weight
    100.163 kDa
    Gene ID
    54453
    UniProt
    Q8WYP3
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