SIX Homeobox 1 antibody (C-Term) (FITC)

Catalog No. ABIN8037876

The Rabbit Polyclonal anti-SIX Homeobox 1 antibody is suitable to detect SIX Homeobox 1 in samples from Human. It has been validated for FACS.

Quick Overview for SIX Homeobox 1 antibody (C-Term) (FITC) (ABIN8037876)

Target: SIX Homeobox 1 (SIX1)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SIX Homeobox 1 antibody is conjugated to FITC

Application: Flow Cytometry (FACS)

Product Details anti-SIX Homeobox 1 Antibody (FITC)

Binding Specificity: C-Term

Purpose: Anti-SIX1 Antibody FITC Conjugated

Specificity: No cross reactivity with other proteins.

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Predicted Reactivity: different from the related mouse sequence by one amino acid.

Purification: Immunogen affinity purified.

Immunogen: A synthetic peptide corresponding to a sequence at the C-terminus of human SIX1, different from the related mouse sequence by one amino acid.

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Expiry Date: 12 months

Target Details for SIX Homeobox 1

Target: SIX Homeobox 1 (SIX1)

Alternative Name: SIX1

Background:

Background: Homeobox protein SIX1 (Sineoculis homeobox homolog 1) is a protein that in humans is encoded by the SIX1 gene. It is mapped to 14q23.1. 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).

Gene Full Name: SIX homeobox 1

Gene ID: 6495

UniProt: Q15475

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