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

Fukutin antibody

The Rabbit Polyclonal anti-Fukutin antibody (ABIN7248716) specifically detects Fukutin in WB and ELISA. The antibody is reactive with Human and Mouse samples.
Catalog No. ABIN7248716
-15% Promotion 2026
$457.98
$538.80
save $80.82 (-15 %)
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for Fukutin antibody (ABIN7248716)

Target

See all Fukutin (FKTN) Antibodies
Fukutin (FKTN)

Reactivity

  • 48
  • 33
  • 18
  • 6
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Human, Mouse

Host

  • 48
  • 1
Rabbit

Clonality

  • 37
  • 12
Polyclonal

Conjugate

  • 25
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
This Fukutin antibody is un-conjugated

Application

  • 39
  • 26
  • 15
  • 6
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human FKTN

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.08 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    Fukutin (FKTN)

    Alternative Name

    FKTN

    Background

    The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 54 kDa

    UniProt

    O75072

    Pathways

    Regulation of Carbohydrate Metabolic Process
You are here:
Chat with us!