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METTL7A antibody

This anti-METTL7A antibody is a Rabbit Polyclonal antibody detecting METTL7A in WB and IHC. Suitable for Human and Rat.
Catalog No. ABIN7264251

Quick Overview for METTL7A antibody (ABIN7264251)

Target

See all METTL7A Antibodies
METTL7A (Methyltransferase Like 7A (METTL7A))

Reactivity

  • 28
  • 6
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Rat

Host

  • 27
  • 1
Rabbit

Clonality

  • 28
Polyclonal

Conjugate

  • 13
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This METTL7A antibody is un-conjugated

Application

  • 15
  • 12
  • 9
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human METTL7A (NP_054752.3).

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000 IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    METTL7A (Methyltransferase Like 7A (METTL7A))

    Alternative Name

    METTL7A

    Background

    METTL7A (methyltransferase like 7A), also known as AAM-B, is a 244 amino acid protein that is thought to function as a methyltransferase and is encoded by a gene which maps to chromosome 12. Encoding over 1,100 genes, chromosome 12 comprises nearly 4.5 % of the human genome and is associated with a number of skeletal deformaties, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to both a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and a natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Additionally, Trisomy 12p (three copies of the p arm of chromosome 12) leads to facial developmental defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism.

    Molecular Weight

    Observed_MW: 28 kDa

    Calculated_MW: 28 kDa

    Gene ID

    25840

    UniProt

    Q9H8H3
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