Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Tricellulin antibody

MARVELD2 Reactivity: Human, Rat, Mouse WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7264717
  • Target See all Tricellulin (MARVELD2) Antibodies
    Tricellulin (MARVELD2)
    Reactivity
    • 32
    • 11
    • 10
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Rat, Mouse
    Host
    • 32
    Rabbit
    Clonality
    • 32
    Polyclonal
    Conjugate
    • 15
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Tricellulin antibody is un-conjugated
    Application
    • 24
    • 15
    • 14
    • 3
    • 2
    • 2
    Western Blotting (WB), Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide of human MARVELD2 (NP_001033692.2).
    Isotype
    IgG
  • Application Notes
    WB 1:500-1:2000 IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 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
    Store at -20°C. Avoid freeze / thaw cycles.
  • 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
    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

    Observed_MW: 64 kDa

    Calculated_MW: 51 kDa/62 kDa/64 kDa

    Gene ID
    153562
    UniProt
    Q8N4S9
    Pathways
    Sensory Perception of Sound, Cell-Cell Junction Organization
You are here:
Support