NPHS2 polyclonal antibody

Catalog # PAB14847

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Price

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Quantity

Size:100 ug
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Tissue lysate)
Application

Western Blot (Tissue lysate)

Western blot analysis of rat kidney tissue lysate with NPHS2 polyclonal antibody (Cat # PAB14847).

  • Specification

    Product Description

    Rabbit polyclonal antibody raised against synthetic peptide of NPHS2.

    Immunogen

    A synthetic peptide corresponding to amino acids at internal region of human NPHS2.

    Host

    Rabbit

    Theoretical MW (kDa)

    42, 34

    Reactivity

    Human, Mouse, Rat

    Specificity

    Different from the mouse sequence by one aminoacid.

    Form

    Lyophilized

    Purification

    Affinity purification

    Isotype

    IgG

    Recommend Usage

    Western Blot (1 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    Lyophilized from 0.9 mg NaCl, 0.2 mg Na2HPO4 (5 mg BSA, 0.05 mg sodium azide, 0.05 mg Thimerosal)

    Storage Instruction

    Store at -20°C on dry atmosphere.
    After reconstitution with 200 uL of deionized water and concentration will be 500 ug/mL, store at -20°C or lower.
    Aliquot to avoid repeated freezing and thawing.

    Note

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

  • Applications

    Western Blot (Tissue lysate)

    Western blot analysis of rat kidney tissue lysate with NPHS2 polyclonal antibody (Cat # PAB14847).
  • Gene Info — NPHS2

    Entrez GeneID

    7827

    Gene Name

    NPHS2

    Gene Alias

    PDCN, SRN1

    Gene Description

    nephrosis 2, idiopathic, steroid-resistant (podocin)

    Omim ID

    600995 604766

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes the glomerular protein podocin which plays a role in the regulation of glomerular permeability, and acts as a linker between the plasma membrane and the cytoskeleton. Defects in this gene are the cause of autosomal recessive steroid-resistant nephrotic syndrome (SRN). SRN is characterized by onset between three months and five years, resistance to steroid therapy and rapid progression to end-stage renal disease. An alternative splice variant has been described but its full length sequence has not been determined. [provided by RefSeq

    Other Designations

    OTTHUMP00000033186|podocin

  • 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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