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

PMM2 antibody (AA 1-174)

The Rabbit Polyclonal anti-PMM2 antibody has been validated for WB and IHC. It is suitable to detect PMM2 in samples from Human.
Catalog No. ABIN1885691

Quick Overview for PMM2 antibody (AA 1-174) (ABIN1885691)

Target

See all PMM2 Antibodies
PMM2 (Phosphomannomutase 2 (PMM2))

Reactivity

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

Host

  • 26
  • 5
Rabbit

Clonality

  • 27
  • 3
Polyclonal

Conjugate

  • 25
  • 2
  • 1
  • 1
  • 1
  • 1
This PMM2 antibody is un-conjugated

Application

  • 30
  • 18
  • 6
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 10
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-174

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 174 (O15305) of PMM2
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.250

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    PMM2 (Phosphomannomutase 2 (PMM2))

    Alternative Name

    Phosphomannomutase 2

    Background

    The protein encoded by this gene catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate, which is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides.Mutations in this gene have been shown to cause defects in glycoprotein biosynthesis, which manifests as carbohydrate-deficient glycoprotein syndrome type I.[provided by RefSeq]

    Molecular Weight

    28 kDa

    Gene ID

    5373
You are here:
Chat with us!