Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Microphthalmia-Associated Transcription Factor (MITF) (Middle Region) Peptide

MITF Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN2184035

Quick Overview for Microphthalmia-Associated Transcription Factor (MITF) (Middle Region) Peptide (ABIN2184035)

Target

MITF (Microphthalmia-Associated Transcription Factor (MITF))

Origin

Human

Source

  • 3
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Sequence

    NSNCEKEGFY KFEEQNRAES ECPGMNTHSR ASCMQMDDVI DDIISLESSY

    Characteristics

    This is a synthetic peptide designed for use in combination with anti-MITF Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handling Advice

    Avoid repeat freeze-thaw cycles.

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    MITF (Microphthalmia-Associated Transcription Factor (MITF))

    Background

    MITF is 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.

    Alias Symbols: CMM8, MI, WS2, WS2A, bHLHe32

    Protein Size: 357

    Molecular Weight

    39 kDa

    Gene ID

    4286

    NCBI Accession

    NM_198178, NP_937821
You are here:
Chat with us!