VSX1 antibody

Catalog No. ABIN7232124

The Rabbit Polyclonal anti-VSX1 antibody (ABIN7232124) specifically detects VSX1 in WB and ELISA. The antibody is reactive with Human and Mouse samples.

Quick Overview for VSX1 antibody (ABIN7232124)

Target: VSX1 (Visual System Homeobox 1 (VSX1))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This VSX1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-VSX1 Antibody

Purpose: Rabbit Anti-VSX1 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of VSX1 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human VSX1 protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for VSX1

Target: VSX1 (Visual System Homeobox 1 (VSX1))

Alternative Name: VSX1

Background: Visual system homeobox 1, Homeodomain protein RINX, Retinal inner nuclear layer homeobox protein, Transcription factor VSX1VSX1 encoded by this gene contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described. VSX1 (Visual System Homeobox 1) is a Protein Coding gene. Diseases associated with VSX1 include Keratoconus 1 and Craniofacial Anomalies And Anterior Segment Dysgenesis Syndrome.

Molecular Weight: 40kD

Gene ID: 30813

UniProt: Q9NZR4