FOXC1 antibody (AA 392-554) (FITC)

Catalog No. ABIN7991375

The FITC-conjugated Rabbit Polyclonal anti-FOXC1 antibody (ABIN7991375) specifically detects FOXC1 in FACS. The antibody is reactive with Human samples.

Quick Overview for FOXC1 antibody (AA 392-554) (FITC) (ABIN7991375)

Target: FOXC1 (Forkhead Box C1 (FOXC1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FOXC1 antibody is conjugated to FITC

Application: Flow Cytometry (FACS)

Product Details anti-FOXC1 Antibody (FITC)

Binding Specificity: AA 392-554

Purpose: Anti-FOXC1 Antibody FITC Conjugated

Specificity: No cross reactivity with other proteins.

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

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human FOXC1 recombinant protein (Position: T392-F554).

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 FOXC1

Target: FOXC1 (Forkhead Box C1 (FOXC1))

Alternative Name: FOXC1

Background:

Background: Forkhead box C1, also known as?FOXC1, is a?protein?which in humans is encoded by the?FOXC1?gene. It is mapped to 6p25.3. This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined, however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.

Gene Full Name: forkhead box C1

Gene ID: 2296

UniProt: Q12948

Pathways: Chromatin Binding, Glycosaminoglycan Metabolic Process