Tricellulin antibody (AA 170-250)

Catalog No. ABIN7229556

The Rabbit Polyclonal anti-Tricellulin antibody (ABIN7229556) specifically detects Tricellulin in WB and ELISA. The antibody is reactive with Human and Mouse samples.

Quick Overview for Tricellulin antibody (AA 170-250) (ABIN7229556)

Target: Tricellulin (MARVELD2)

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Tricellulin antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-Tricellulin Antibody

Binding Specificity: AA 170-250

Purpose: Rabbit Anti-MALD2 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of MALD2 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 MALD2 protein at AA range: 170-250

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 Tricellulin

Target: Tricellulin (MARVELD2)

Alternative Name: MALD2

Background: MARVEL domain-containing protein 2, TricellulinThe protein encoded by MARVELD2 (MARVEL Domain Containing 2) is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in MARVELD2 are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for MARVELD2.

Molecular Weight: 61kD

Gene ID: 153562

UniProt: Q8N4S9

Pathways: Sensory Perception of Sound, Cell-Cell Junction Organization