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GLDC antibody (N-Term)

The Rabbit Polyclonal anti-GLDC antibody has been validated for WB and EIA. It is suitable to detect GLDC in samples from Human and Mouse.
Catalog No. ABIN952523

Quick Overview for GLDC antibody (N-Term) (ABIN952523)

Target

See all GLDC Antibodies
GLDC (Glycine Dehydrogenase (GLDC))

Reactivity

  • 46
  • 17
  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 50
  • 2
Rabbit

Clonality

  • 50
  • 2
Polyclonal

Conjugate

  • 26
  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GLDC antibody is un-conjugated

Application

  • 48
  • 18
  • 15
  • 14
  • 13
  • 13
  • 12
  • 5
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 15
    • 8
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 56-85, N-Term

    Specificity

    This antibody recpognizes Human and Mouse GLDC (N-term).

    Purification

    Protein A column, followed by peptide affinity purification

    Immunogen

    KLH conjugated synthetic peptide between 56~85 amino acids from the N-terminal region of Human GLDC

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    GLDC (Glycine Dehydrogenase (GLDC))

    Alternative Name

    GLDC

    Background

    Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).Synonyms: GCSP, Glycine cleavage system P protein, Glycine decarboxylase, Glycine dehydrogenase [decarboxylating], mitochondrial

    Molecular Weight

    112730 Da

    Gene ID

    2731

    NCBI Accession

    NP_000161
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