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SIX Homeobox 1 (SIX1) (Middle Region) Peptid

SIX1 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN983778

Kurzübersicht für SIX Homeobox 1 (SIX1) (Middle Region) Peptid (ABIN983778)

Target

SIX Homeobox 1 (SIX1)

Spezies

Human

Quelle

  • 3
Synthetic

Applikation

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

    Middle Region

    Produktmerkmale

    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.

    Aufreinigung

    Purified
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Konzentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    SIX Homeobox 1 (SIX1)

    Hintergrund

    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

    Molekulargewicht

    32 kDa

    Gen-ID

    6495

    NCBI Accession

    NM_005982, NP_005973

    UniProt

    Q15475
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