MITF monoclonal antibody, clone D5 + MITF/915

Catalog # MAB21306

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Price

Stock

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 of human melanoma.

  • Specification

    Product Description

    Mouse monoclonal antibody raised against human MITF.

    Immunogen

    NH2 terminus fragment of human Mi protein (D5) and recombinant human MiTF protein (MITF/915).

    Host

    Mouse

    Reactivity

    Human

    Form

    Liquid

    Purification

    Protein A/G purification

    Isotype

    IgG

    Recommend Usage

    Flow Cytometry (0.5-1 ug/million cells in 0.1 mL)
    Immunofluorescence (0.5-1 ug/mL)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (0.5-1 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 1 mg/mL 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 of human melanoma.

    Immunofluorescence

    Flow Cytometry

  • Gene Info — MITF

    Entrez GeneID

    4286

    Protein Accession#

    O75030

    Gene Name

    MITF

    Gene Alias

    MI, WS2A, bHLHe32

    Gene Description

    microphthalmia-associated transcription factor

    Omim ID

    103470 103500 156845 193510

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. It regulates the differentiation and development of melanocytes retinal pigment epithelium and is also responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq

    Other Designations

    OTTHUMP00000195123|OTTHUMP00000195140|homolog of mouse microphthalmia

  • Interactome
  • Pathway
  • 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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