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Glycogen Synthase 1 antibody

Cited in 1 publication. The Mouse Monoclonal anti-Glycogen Synthase 1 antibody (Clone 3A7) (ABIN969183) specifically detects Glycogen Synthase 1 in WB, ELISA and FACS. The antibody is reactive with Human samples.
Catalog No. ABIN969183
$548.16
Plus shipping costs $50.00
100 μL
Shipping to: United States
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Quick Overview for Glycogen Synthase 1 antibody (ABIN969183)

Target

See all Glycogen Synthase 1 (GYS1) Antibodies
Glycogen Synthase 1 (GYS1) (Glycogen Synthase 1 (Muscle) (GYS1))

Reactivity

  • 82
  • 58
  • 32
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 82
  • 1
Mouse

Clonality

  • 46
  • 37
Monoclonal

Conjugate

  • 42
  • 5
  • 5
  • 5
  • 5
  • 5
  • 5
  • 5
  • 3
  • 3
This Glycogen Synthase 1 antibody is un-conjugated

Application

  • 68
  • 37
  • 33
  • 26
  • 24
  • 9
  • 7
  • 6
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Clone

3A7
  • Purpose

    GYS1 Antibody

    Purification

    Ascitic fluid

    Immunogen

    Purified recombinant fragment of human GYS1 expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Ascitic fluid containing 0.03 % 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

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Luttjeboer, Harada, Hughes, Johnson, Lilford, Mol: "Tubal flushing for subfertility." in: Cochrane database of systematic reviews (Online), Issue 3, pp. CD003718, (2007) (PubMed).

  • Target

    Glycogen Synthase 1 (GYS1) (Glycogen Synthase 1 (Muscle) (GYS1))

    Alternative Name

    GYS1

    Background

    Glycogen synthase, skeletal muscle, the rate limiting enzyme of the insulin-induced glycogenesis. The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1, 4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Muscle GS is expressed in several tissues.

    Molecular Weight

    85 kDa

    Gene ID

    2997

    UniProt

    P13807

    Pathways

    PI3K-Akt Signaling, AMPK Signaling, Cellular Glucan Metabolic Process
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