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SIX Homeobox 1 antibody (AA 1-284)

The Mouse Monoclonal anti-SIX Homeobox 1 antibody (Clone 1H4) (ABIN2732097) specifically detects SIX Homeobox 1 in WB. The antibody is reactive with Human samples.
Catalog No. ABIN2732097
$608.40
Plus shipping costs $50.00
0.1 mL
Shipping to: United States
Delivery in 6 to 9 Business Days

Quick Overview for SIX Homeobox 1 antibody (AA 1-284) (ABIN2732097)

Target

See all SIX Homeobox 1 (SIX1) Antibodies
SIX Homeobox 1 (SIX1)

Reactivity

  • 31
  • 20
  • 14
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 27
  • 4
Mouse

Clonality

  • 28
  • 3
Monoclonal

Conjugate

  • 20
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SIX Homeobox 1 antibody is un-conjugated

Application

  • 17
  • 13
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB)

Clone

1H4
  • Binding Specificity

    • 6
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-284

    Characteristics

    Homo sapiens SIX homeobox 1 (SIX1)

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Human recombinant protein fragment corresponding to amino acids 1-284 of human SIX1(NP_005973) produced in E.coli.

    Isotype

    IgG1
  • Application Notes

    WB 1:2000,

    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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

    -20 °C
  • Target

    SIX Homeobox 1 (SIX1)

    Alternative Name

    SIX1

    Background

    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).

    Molecular Weight

    32 kDa

    Gene ID

    6495

    NCBI Accession

    NM_005982

    HGNC

    6495

    Pathways

    Sensory Perception of Sound, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
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