CEACAM16 antibody (AA 201-300) (FITC)

Catalog No. ABIN889912

This Rabbit Polyclonal antibody specifically detects CEACAM16 in WB, IF (cc) and IF (p). It exhibits reactivity toward Human.

Quick Overview for CEACAM16 antibody (AA 201-300) (FITC) (ABIN889912)

Target: CEACAM16 (Carcinoembryonic Antigen-Related Cell Adhesion Molecule 16 (CEACAM16))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CEACAM16 antibody is conjugated to FITC

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-CEACAM16 Antibody (FITC)

Binding Specificity: AA 201-300

Predicted Reactivity: Human,Mouse,Rat,Cow,Pig,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CEACAM16

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for CEACAM16

Target: CEACAM16 (Carcinoembryonic Antigen-Related Cell Adhesion Molecule 16 (CEACAM16))

Alternative Name: CEACAM16

Background:

Synonyms: Carcinoembryonic antigen like 2, Carcinoembryonic antigen like 2 protein, Carcinoembryonic antigen related cell adhesion molecule 16, CEAL2, CEA16_HUMAN.

Background: The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012].

Gene ID: 388551

Pathways: Sensory Perception of Sound