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Rabbit anti-Human PMM2 Polyclonal Antibody

The antibody against PMM2 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-246 of human PMM2 (NP_000294.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

ADA-04020A

The antibody against PMM2 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-246 of human PMM2 (NP_000294.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

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Specifications


Cat.No ADA-04020A ClonalityPolyclonal
Host SpeciesRabbitTarget NamePMM2
Target SynonymsPMI; CDG1; CDGS; PMI1; CDG1a; PMM 2; PMM2FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesHeLa, NIH/3T3, Rat brain, 293T, A-549, HepG2, Mouse intestine, Mouse liverApplicationELISA, WB, IF/ICC

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 1-246 of human PMM2 (NP_000294.1).Target SpeciesHuman
Uniprot IDO15305Immunogen Sequence
Background Information
  • Uniprot Id

    O15305

  • Target Species

    Human

  • Target Name

    PMM2

  • Target Full Name

    Phosphomannomutase 2

  • Target Function

    Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions.

  • Target Involvement

    Congenital disorder of glycosylation 1A (CDG1A)

  • Target Subcellular Location

    Cytoplasm.

  • Target Protein Families

    Eukaryotic PMM family

  • Target Research Area

    Signal Transduction

  • Target Synonyms

    AI585868; BOS_22465; C86848; CDG 1; CDG1; CDG1a; CDGS; MGC127449; Phosphomannomutase 2; PMM 2; Pmm2; PMM2_HUMAN

  • Target 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.

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