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

GLDC antibody (N-Term)

This anti-GLDC antibody is a Rabbit Polyclonal antibody detecting GLDC in WB. Suitable for Human and Mouse.
Catalog No. ABIN653448

Quick Overview for GLDC antibody (N-Term) (ABIN653448)

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
  • 1
Western Blotting (WB)

Clone

RB23981
  • Binding Specificity

    • 15
    • 7
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 49-77, N-Term

    Purification

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

    Immunogen

    This GLDC antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 49-77 amino acids from the N-terminal region of human GLDC.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. 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

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • 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).

    Molecular Weight

    112730

    Gene ID

    2731

    NCBI Accession

    NP_000161

    UniProt

    P23378
You are here:
Chat with us!