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Methylglyoxal Modified Proteins antibody

The Mouse Monoclonal anti-Methylglyoxal Modified Proteins antibody (Clone MGO-1) (ABIN1108230) specifically detects Methylglyoxal Modified Proteins in IHC (p), WB and EIA. The antibody is reactive with Various Species samples.
Catalog No. ABIN1108230
$942.00
Plus shipping costs $50.00
0.1 mg
Shipping to: United States
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Quick Overview for Methylglyoxal Modified Proteins antibody (ABIN1108230)

Target

Methylglyoxal Modified Proteins

Reactivity

Various Species

Host

  • 1
Mouse

Clonality

  • 1
Monoclonal

Conjugate

  • 1
Un-conjugated

Application

Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB), Enzyme Immunoassay (EIA)

Clone

MGO-1
  • Cross-Reactivity (Details)

    Species reactivity (tested):Human. Multispecies cross reactant.

    Purification

    Protein G

    Immunogen

    MGO-modified KLH

    Isotype

    IgG1
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    0.1 mg/mL

    Buffer

    PBS, 0.02 % sodium azide, 0.1 % bovine serum albumin

    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

    Storage Comment

    Store at 2 - 8 °C.
  • Target

    Methylglyoxal Modified Proteins

    Background

    Methylglyoxal (MGO) is an endogenous product of glucose metabolism. Increased production and accumulation of methylglyoxal (MGO), as well as increased modification of proteins by glycoxidation, are hallmarks of aging and diabetes. MGO was shown to modify proteins and to contribute to the accumulation of damaged proteins that can be toxic to cells. A number of studies have shown that MGO levels are significantly elevated in patients with Type 2 Diabetes and correlates well with fasting plasma glucose and hemoglobin A1c (HbA1c) levels. Moreover, increased formation of the MGO is implicated in renal dysfunction and is known to be involved in the development of DN (diabetic nephropathy).
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