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Six5 antibody (AA 257-286)

This Rabbit Polyclonal antibody specifically detects Six5 in WB, IF and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN656668

Quick Overview for Six5 antibody (AA 257-286) (ABIN656668)

Target

See all Six5 (SIX5) Antibodies
Six5 (SIX5) (Homeobox protein SIX5 (SIX5))

Reactivity

  • 22
  • 12
  • 1
Human

Host

  • 23
Rabbit

Clonality

  • 23
Polyclonal

Conjugate

  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Six5 antibody is un-conjugated

Application

  • 16
  • 13
  • 8
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB32413
  • Binding Specificity

    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 257-286

    Predicted Reactivity

    M

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This SIX5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 257-286 amino acids from the Central region of human SIX5.

    Isotype

    Ig Fraction
  • Application Notes

    IF: 1:10~50. WB: 1:1000. IHC-P: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    SIX5 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Expiry Date

    6 months
  • Target

    Six5 (SIX5) (Homeobox protein SIX5 (SIX5))

    Alternative Name

    SIX5

    Background

    The protein encoded by this gene is a homeodomain-containing transcription factor that appears to function in the regulation of organogenesis. This gene is located downstream of the dystrophia myotonica-protein kinase gene. Mutations in this gene are a cause of branchiootorenal syndrome type 2.

    Molecular Weight

    74562

    Gene ID

    147912

    NCBI Accession

    NP_787071

    UniProt

    Q8N196
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