SOX14 antibody

Catalog No. ABIN2461192

This Rabbit Polyclonal antibody specifically detects SOX14 in WB and ELISA. It exhibits reactivity toward Human, Mouse, Rat, Zebrafish (Danio rerio) and Dog.

Quick Overview for SOX14 antibody (ABIN2461192)

Target: SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))

Reactivity: Human, Mouse, Rat, Zebrafish (Danio rerio), Dog

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SOX14 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-SOX14 Antibody

Purification: Antibody is purified by protein A chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SOX14.

Application Details

Application Notes: SOX14 antibody can be used for detection of SOX14 by ELISA at 1:62500. SOX14 antibody can be used for detection of SOX14 by western blot at 1.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

Storage Comment: For short periods of storage (days) store at 4 °C. For longer periods of storage, store SOX14 antibody at -20 °C.

Target Details for SOX14

Target: SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))

Alternative Name: SOX14

Background: SOX14 encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in SOX14 are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome.

Molecular Weight: 26 kDa

Gene ID: 8403

NCBI Accession: NP_004180

UniProt: O95416