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NAD-ME antibody (C-Term)

This anti-NAD-ME antibody is a Rabbit Polyclonal antibody detecting NAD-ME in WB and IHC (p). Suitable for Human and Mouse.
Catalog No. ABIN656541

Quick Overview for NAD-ME antibody (C-Term) (ABIN656541)

Target

See all NAD-ME Antibodies
NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))

Reactivity

  • 31
  • 15
  • 5
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 29
  • 2
Rabbit

Clonality

  • 29
  • 2
Polyclonal

Conjugate

  • 22
  • 3
  • 2
  • 2
  • 1
  • 1
This NAD-ME antibody is un-conjugated

Application

  • 24
  • 19
  • 16
  • 7
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB32070
  • Binding Specificity

    • 7
    • 6
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 527-556, C-Term

    Purification

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

    Immunogen

    This ME2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 527-556 amino acids from the C-terminal region of human ME2.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. IHC-P: 1:10~50

    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

    ME2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Expiry Date

    6 months
  • Target

    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))

    Alternative Name

    ME2

    Background

    This gene encodes a mitochondrial NAD-dependent malic enzyme, a homotetrameric protein, that catalyzes the oxidative decarboxylation of malate to pyruvate. It had previously been weakly linked to a syndrome known as Friedreich ataxia that has since been shown to be the result of mutation in a completely different gene. Certain single-nucleotide polymorphism haplotypes of this gene have been shown to increase the risk for idiopathic generalized epilepsy. Alternatively spliced transcript variants encoding different isoforms found for this gene. [provided by RefSeq].

    Molecular Weight

    65444

    Gene ID

    4200

    NCBI Accession

    NP_001161807, NP_002387

    UniProt

    P23368

    Pathways

    Production of Molecular Mediator of Immune Response
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