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Rabbit anti-Human Phospho-GYS1-S641 Polyclonal Antibody

The antibody against Phospho-GYS1-S641 was raised in Rabbit using a synthetic phosphorylated peptide around S641 of human Glycogen synthase 1 (GYS1) (NP_002094.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-10355A

The antibody against Phospho-GYS1-S641 was raised in Rabbit using a synthetic phosphorylated peptide around S641 of human Glycogen synthase 1 (GYS1) (NP_002094.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-10355A ClonalityPolyclonal
Host SpeciesRabbitTarget NamePhospho-GYS1-S641
Target SynonymsGSY; GYS; Phospho-GYS1-S641FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.01% thimerosal, pH7.3.Purification MethodAffinity purification
Positive SamplesC6, NIH/3T3, 293TApplicationELISA, WB

Immunogen Information


Immunogen DescriptionA synthetic phosphorylated peptide around S641 of human Glycogen synthase 1 (GYS1) (NP_002094.2).Target SpeciesHuman
Immunogen SequencePASVPUniprot IDP13807
Background Information
  • Uniprot Id

    P13807

  • Target Species

    Human

  • Target Name

    GYS1

  • Target Full Name

    Glycogen [starch] synthase, muscle

  • Target Function

    Transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan.

  • Target Involvement

    Muscle glycogen storage disease 0 (GSD0b)

  • Target Protein Families

    Glycosyltransferase 3 family

  • Target Synonyms

    Glycogen [starch] synthase; Glycogen synthase 1 (muscle); Glycogen synthase 1; GSY; GYS; Gys1; GYS1_HUMAN; muscle

  • Target Background

    The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1, 4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

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