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

DMGDH antibody (C-Term)

This anti-DMGDH antibody is a Rabbit Polyclonal antibody detecting DMGDH in WB. Suitable for Human.
Catalog No. ABIN1537626

Quick Overview for DMGDH antibody (C-Term) (ABIN1537626)

Target

See all DMGDH Antibodies
DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Reactivity

  • 31
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 31
Rabbit

Clonality

  • 31
Polyclonal

Conjugate

  • 16
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DMGDH antibody is un-conjugated

Application

  • 21
  • 18
  • 6
  • 3
  • 1
  • 1
Western Blotting (WB)

Clone

RB23867
  • Binding Specificity

    • 7
    • 7
    • 6
    • 1
    • 1
    • 1
    • 1
    AA 836-864, C-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This DMGDH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 836-864 amino acids from the C-terminal region of human DMGDH.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    DMGDH Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • Target

    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

    Alternative Name

    DMGDH

    Background

    This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum.

    Molecular Weight

    96811

    Gene ID

    29958

    NCBI Accession

    NP_037523

    UniProt

    Q9UI17
You are here:
Chat with us!