MITF monoclonal antibody, clone C5

Catalog # MAB1955

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Size:100 ug
Price: USD $ 850.00
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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 usin MITF monoclonal antibody, clone C5 (Cat # MAB1955) on formalin fixed, paraffin embedded human melanoma.

  • Specification

    Product Description

    Mouse monoclonal antibody raised against partial recombinant MITF.

    Immunogen

    Recombinant protein corresponding to N-terminus of human MITF.

    Host

    Mouse

    Reactivity

    Human, Mouse, Rat

    Form

    Liquid

    Isotype

    IgG1

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Recommend Usage

    Western blot (1 ug/mL)
    Immunoprecipitation (2 ug/mg of protein lysate)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS (0.08% sodium azide)

    Storage Instruction

    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

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

    Immunohistochemical staining usin MITF monoclonal antibody, clone C5 (Cat # MAB1955) on formalin fixed, paraffin embedded human melanoma.

    Immunohistochemistry (Frozen sections)

    Immunoprecipitation

    Gel Supershift Assay

  • Gene Info — MITF

    Entrez GeneID

    4286

    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
  • 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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