×
For best experience we recommend to activate Javascript in your browser.
Tricellulin antibody
MARVELD2
Reactivity: Human, Rat, Mouse
WB, IHC, ELISA
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-Tricellulin Antibody
(hide)
Target
See all Tricellulin (MARVELD2) Antibodies
Tricellulin (MARVELD2)
Reactivity
All reactivities for Tricellulin antibodies
Human, Rat, Mouse
Host
All hosts for Tricellulin antibodies
Rabbit
Clonality
All clonalities for Tricellulin antibodies
Polyclonal
Conjugate
All conjugates for Tricellulin antibodies
This Tricellulin antibody is un-conjugated
Application
All applications for Tricellulin antibodies
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
Purification
Immunogen affinity purified
Purity
≥95 % as determined by SDS-PAGE
Immunogen
MARVEL domain containing 2
Isotype
IgG
Top Product
Discover our top product MARVELD2 Primary Antibody
Alternatives
(show)
Application Details
(hide)
Application Notes
WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
Restrictions
For Research Use only
Handling
(hide)
Format
Liquid
Buffer
PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
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
-20°C for 12 months (Avoid repeated freeze / thaw cycles.)
Expiry Date
12 months
Target Details for Tricellulin
(hide)
Target
Tricellulin (MARVELD2)
Alternative Name
MARVELD2 (MARVELD2 Products )
Synonyms
Mrvldc2 antibody, BC003296 antibody, MARVD2 antibody, Tric antibody, Trica antibody, Tricb antibody, Tricc antibody, DFNB49 antibody, MRVLDC2 antibody, MARVEL domain containing 2 antibody, MARVEL (membrane-associating) domain containing 2 antibody, Marveld2 antibody, MARVELD2 antibody
Background
Synonyms:TRIC 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.
Molecular Weight
69 kDa
Gene ID
153562
UniProt
Q8N4S9
Pathways
Sensory Perception of Sound , Cell-Cell Junction Organization
Recently viewed
(hide)