Tricellulin antibody (AA 170-250)

Catalog No. ABIN7229556

This anti-Tricellulin antibody is a Rabbit Polyclonal antibody detecting Tricellulin in WB and ELISA. Suitable for Human and Mouse.

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: MALD2 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of MALD2 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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 (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: 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.

Target Details for Tricellulin

Target: Tricellulin (MARVELD2)

Alternative Name: MALD2

Background: Rabbit Anti-MALD2 Polyclonal Antibody,MARVEL domain-containing protein 2, Tricellulin,The 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.,MALD2

Molecular Weight: observerd band 61kDa

Gene ID: 153562

UniProt: Q8N4S9

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