VSX2 antibody (AA 70-150)

Catalog No. ABIN7232126

The Rabbit Polyclonal anti-VSX2 antibody is suitable to detect VSX2 in samples from Human and Mouse. It has been validated for WB and ELISA.

Quick Overview for VSX2 antibody (AA 70-150) (ABIN7232126)

Target: VSX2 (Visual System Homeobox 2 (VSX2))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This VSX2 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-VSX2 Antibody

Binding Specificity: AA 70-150

Purpose: Rabbit Anti-VSX2 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of VSX2 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 VSX2 protein at AA range: 70-150

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 VSX2

Target: VSX2 (Visual System Homeobox 2 (VSX2))

Alternative Name: VSX2

Background: Visual system homeobox 2, Ceh-10 homeodomain-containing homolog Homeobox protein CHX10VSX2 (Visual System Homeobox 2) is a Protein Coding gene. Diseases associated with VSX2 include Microphthalmia, Isolated 2 and Microphthalmia With Coloboma 3. VSX2 encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in VSX2 are associated with microphthalmia, cataracts and iris abnormalities.

Molecular Weight: 39kD

Gene ID: 338917

UniProt: P58304

Pathways: Dopaminergic Neurogenesis