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TMC6 antibody (AA 1-772) (Fluoro488)

This Rabbit Polyclonal antibody specifically detects TMC6 in FACS. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN8048879
$590.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for TMC6 antibody (AA 1-772) (Fluoro488) (ABIN8048879)

Target

See all TMC6 Antibodies
TMC6 (Transmembrane Channel-Like 6 (TMC6))

Reactivity

Human, Mouse, Rat

Host

  • 26
Rabbit

Clonality

  • 26
Polyclonal

Conjugate

  • 12
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
This TMC6 antibody is conjugated to Fluoro488

Application

  • 19
  • 13
  • 10
  • 5
  • 4
  • 3
  • 3
  • 1
Flow Cytometry (FACS)
  • Binding Specificity

    • 12
    • 8
    • 4
    • 2
    • 2
    • 2
    • 1
    AA 1-772

    Purpose

    Anti-TMC6 Antibody Fluoro488 Conjugated

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins

    Predicted Reactivity

    Human TMC6 shares 76.7% amino acid (aa) sequence identity with mouse TMC6.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human TMC6 recombinant protein (Position: M1-H772). Human TMC6 shares 76.7% amino acid (aa) sequence identity with mouse TMC6.

    Isotype

    IgG
  • Application Notes

    Flow Cytometry, Optimal dilutions should be determined by end users.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    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

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    Expiry Date

    12 months
  • Target

    TMC6 (Transmembrane Channel-Like 6 (TMC6))

    Alternative Name

    TMC6

    Background

    Background: Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25.3. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane channels. This gene encodes a transmembrane channel-like protein with 10 transmembrane domains and 2 leucine zipper motifs.

    Gene Full Name: transmembrane channel like 6

    Gene ID

    11322

    UniProt

    Q7Z403
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