SATB2 antibody (AA 650-730)

Catalog No. ABIN7231262

This Rabbit Polyclonal antibody specifically detects SATB2 in WB and ELISA. It exhibits reactivity toward Human and Mouse.

Quick Overview for SATB2 antibody (AA 650-730) (ABIN7231262)

Target: SATB2 (SATB Homeobox 2 (SATB2))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SATB2 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-SATB2 Antibody

Binding Specificity: AA 650-730

Purpose: Rabbit Anti-SATB2 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of SATB2 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 SATB2 protein at AA range: 650-730

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 SATB2

Target: SATB2 (SATB Homeobox 2 (SATB2))

Alternative Name: SATB2

Background: DNA-binding protein SATB2, Special AT-rich sequence-binding protein 2SATB2 (SATB Homeobox 2) is a Protein Coding gene. Diseases associated with SATB2 include Glass Syndrome and Satb2-Associated Syndrome. SATB2 encodes a DNA binding protein that specifically binds nuclear matrix attachment regions. The encoded protein is involved in transcription regulation and chromatin remodeling. Defects in SATB2 are associated with isolated cleft palate and cognitive disability. Alternate splicing results in multiple transcript variants that encode the same protein.

Molecular Weight: 80kD

Gene ID: 23314

UniProt: Q9UPW6