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MALD2 rabbit pAb

The protein encoded by this gene 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 this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011],

Product Specifications

Background

The protein encoded by this gene 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 this gene are a cause of deafness autosomal recessive type 49 (DFNB49) . Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]

UniProt

Q8N4S9

Swiss Prot

Q8N4S9

Reactivity

Human; Mouse

Immunogen

Synthesized peptide derived from human protein . at AA range: 170-250

Clonality

Polyclonal

Source

Rabbit

Applications

WB; ELISA

Concentration

1 mg/ml

Dilution

WB 1:500-2000 ELISA 1:5000-20000

Molecular Weight

61kD

Storage Conditions

-20°C/1 year

Observed Molecular Weight

61kD

Fragment

IgG

Subcellular Location

Cell membrane ; Multi-pass membrane protein . Cell junction, tight junction . Located at tricellular contacts. .

Gene ID (Human)

153562

Available Sizes

Curated Selection

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