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SIX Homeobox 1 (SIX1) (Middle Region) Peptide

SIX1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN983778

Aperçu rapide pour SIX Homeobox 1 (SIX1) (Middle Region) Peptide (ABIN983778)

Antigène

SIX Homeobox 1 (SIX1)

Origine

Humain

Source

  • 3
Synthetic

Application

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

    Middle Region

    Attributs du produit

    This is a synthetic peptide designed for use in combination with anti-SIX1 antibody (Catalog #: ARP32375_P050). 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
  • Indications d'application

    Each Investigator should determine their own optimal working dilution for specific applications.

    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.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

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

    SIX Homeobox 1 (SIX1)

    Sujet

    SIX1 is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3).The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3). Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: BOS3, DFNA23, TIP39

    Protein Interaction Partner: AES,TLE1,AES,CCDC85B,DACH1,EYA1,EYA2,EYA3,EYA4,MDFI,SIX1,TLE1,CCDC85B,EYA1,EYA2,MDFI

    Protein Size: 284

    Poids moléculaire

    32 kDa

    ID gène

    6495

    NCBI Accession

    NM_005982, NP_005973

    UniProt

    Q15475
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