SPTA1 recombinant monoclonal antibody, clone R04-4Z1

Catalog # RAB05628

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Price

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Quantity

Size:100 uL
Price: USD $ 531.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Rabbit recombinant monoclonal antibody raised against human SPTA1.Recombinant Antibody,Recombinant Antibodies,Recombinant Monoclonal Antibody,RecomAb,Recombinant Ab,Recombinant Monoclonal Antibodies,Recombinant Abs

    Antibody Species

    Rabbit

    Immunogen

    Original antibody is raised against corresponding to human SPTA1.

    Theoretical MW (kDa)

    Calculated MW: 280 k

    Reactivity

    Human, Mouse, Rat

    Form

    Liquid

    Isotype

    IgG

    Recommend Usage

    Flow Cytometry (1/50-1/100)
    Immunofluorescence (1/50-1/200)
    Western Blot (1/500-1/1000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, 150mM NaCl, pH 7.4 (50% glycerol and 0.02% sodium azide)

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot

    Immunofluorescence

    Flow Cytometry

  • Gene Info — SPTA1

    Entrez GeneID

    6708

    Gene Name

    SPTA1

    Gene Alias

    EL2, SPTA

    Gene Description

    spectrin, alpha, erythrocytic 1 (elliptocytosis 2)

    Omim ID

    130600 182860 266140 270970

    Gene Ontology

    Hyperlink

    Gene Summary

    Spectrin is an actin crosslinking and molecular scaffold protein that links the plasma membrane to the actin cytoskeleton, and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. It is a tetramer made up of alpha-beta dimers linked in a head-to-head arrangement. This gene is one member of a family of alpha-spectrin genes. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms weaker tetramer interactions than non-erythrocytic alpha spectrin, which may increase the plasma membrane elasticity and deformability of red blood cells. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis type 2, pyropoikilocytosis, and spherocytic hemolytic anemia. [provided by RefSeq

    Other Designations

    OTTHUMP00000021115|alpha-I spectrin|erythrocyte alpha-spectrin|erythroid alpha-spectrin|spectrin alpha chain, erythrocyte|spectrin, alpha, erythrocytic 1

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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