POU3F4 antibody (AA 1-100) (Biotin)

Catalog No. ABIN6982778

The Rabbit Polyclonal anti-POU3F4 antibody is suitable to detect POU3F4 in samples from Human. It has been validated for WB, ELISA, IHC (fro) and IHC (p).

Quick Overview for POU3F4 antibody (AA 1-100) (Biotin) (ABIN6982778)

Target: POU3F4 (POU Domain, Class 3, Transcription Factor 4 (POU3F4))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This POU3F4 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-POU3F4 Antibody (Biotin)

Binding Specificity: AA 1-100

Predicted Reactivity: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human BRN4

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for POU3F4

Target: POU3F4 (POU Domain, Class 3, Transcription Factor 4 (POU3F4))

Alternative Name: BRN4,

Background:

Synonyms: class 3, transcription factor 4, Brain specific homeobox POU domain protein 4, Brain-4, Brain-specific homeobox/POU domain protein 4, BRAIN4, Brn-4, BRN4, DFN3, Oct-9, Octamer-binding protein 9, Octamer-binding transcription factor 9, OTF-9, OTF9, PO3F4_HUMAN, POU domain, POU domain class 3 transcription factor 4, POU3F4.,

Background: Probable transcription factor which exert its primary action widely during early neural development and in a very limited set of neurons in the mature brain.Defects in POU3F4 are a cause of deafness X-linked type 2 (DFNX2) . A mixed type of deafness characterized by both conductive hearing loss resulting from stapes (perilymphatic gusher) fixation and progressive sensorineural deafness.

Gene ID: 5456

UniProt: P49335

Pathways: Sensory Perception of Sound