TYRP1 monoclonal antibody, clone TYRP1/807

Catalog # MAB14624

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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
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human melanoma with TYRP1 monoclonal antibody, clone TYRP1/807 (Cat # MAB14624).

  • Specification

    Product Description

    Mouse monoclonal antibody raised against full length recombinant human TYRP1.

    Immunogen

    Recombinant protein corresponding to full length human TYRP1.

    Host

    Mouse

    Theoretical MW (kDa)

    75

    Reactivity

    Human

    Form

    Liquid

    Purification

    Protein A/G purification

    Isotype

    IgG2a, kappa

    Recommend Usage

    Flow Cytometry (0.5-1 ug/million cells)
    Immunofluorescence (1-2 ug/mL)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (3-6 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 10 mM PBS.

    Storage Instruction

    Store at -20 to -80°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human melanoma with TYRP1 monoclonal antibody, clone TYRP1/807 (Cat # MAB14624).

    Immunofluorescence

    Flow Cytometry

  • Gene Info — TYRP1

    Entrez GeneID

    7306

    Protein Accession#

    P17643

    Gene Name

    TYRP1

    Gene Alias

    CAS2, CATB, GP75, TRP, TYRP, b-PROTEIN

    Gene Description

    tyrosinase-related protein 1

    Omim ID

    115501 203290 278400

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a melanosomal enzyme that belongs to the tyrosinase family and plays an important role in the melanin biosynthetic pathway. Defects in this gene are the cause of rufous oculocutaneous albinism and oculocutaneous albinism type III. [provided by RefSeq

    Other Designations

    associated with iris pigmentation

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