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The antibody against MARVELD2 was raised in rabbit using the Human MARVELD2 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.
The antibody against MARVELD2 was raised in rabbit using the Human MARVELD2 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.
$600.00
| Cat.No | ADC-48025A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | MARVELD2 |
| Target Synonyms | MARVELD2; TRIC; MARVEL domain-containing protein 2; Tricellulin | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.1% Sodium Azide | Purification Method | Antigen affinity purified |
| Conjugate | Non-conjugated | Application | ELISA, WB |
| Storage | Upon receipt |
| Immunogen Description | Human MARVELD2 | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | Q8N4S9 |
Uniprot Id
Q8N4S9
Target Species
Human
Target Name
MARVELD2
Target Full Name
MARVEL domain-containing protein 2
Target Function
Plays a role in the formation of tricellular tight junctions and of epithelial barriers. Required for normal hearing via its role in the separation of the endolymphatic and perilymphatic spaces of the organ of Corti in the inner ear, and for normal survival of hair cells in the organ of Corti.
Target Involvement
Deafness, autosomal recessive, 49 (DFNB49)
Target Subcellular Location
Cell membrane; Multi-pass membrane protein. Cell junction, tight junction.
Target Synonyms
MARVELD2; TRIC; MARVEL domain-containing protein 2; Tricellulin
Target 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.
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