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Tricellulin antibody (AA 1-195)

This anti-Tricellulin antibody is a Rabbit Polyclonal antibody detecting Tricellulin in WB. Suitable for Human.
Catalog No. ABIN6143566

Quick Overview for Tricellulin antibody (AA 1-195) (ABIN6143566)

Target

See all Tricellulin (MARVELD2) Antibodies
Tricellulin (MARVELD2)

Reactivity

  • 28
  • 11
  • 11
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 28
Rabbit

Clonality

  • 28
Polyclonal

Conjugate

  • 15
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Tricellulin antibody is un-conjugated

Application

  • 20
  • 12
  • 11
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-195

    Sequence

    MSNDGRSRNR DRRYDEVPSD LPYQDTTIRT HPTLHDSERA VSADPLPPPP LPLQPPFGPD FYSSDTEEPA IAPDLKPVRR FVPDSWKNFF RGKKKDPEWD KPVSDIRYIS DGVECSPPAS PARPNHRSPL NSCKDPYGGS EGTFSSRKEA DAVFPRDPYG SLDRHTQTVR TYSEKVEEYN LRYSYMKSWA GLLRI

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-195 of human MARVELD2 (NP_001033692.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

    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.,MARVELD2,DFNB49,MARVD2,MRVLDC2,Tric,Signal Transduction,Cell Biology & Developmental Biology,Cell Adhesion,Tight Junctions,Cytoskeleton,MARVELD2

    Molecular Weight

    51 kDa/62 kDa/64 kDa

    Gene ID

    153562

    UniProt

    Q8N4S9

    Pathways

    Sensory Perception of Sound, Cell-Cell Junction Organization
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