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  1. Link

    recombinant-rat-gnas-mutated-q212l--d280n-protein-ab90410.pdf

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Signal Transduction Signaling Pathway G Protein Signaling Heterotrimeric G Proteins G Proteins
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Recombinant Rat GNAS (mutated Q212L + D280N) protein (ab90410)

  • Datasheet
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Key features and details

  • Expression system: Baculovirus infected Sf9 cells
  • Suitable for: Functional Studies

Description

  • Product name

    Recombinant Rat GNAS (mutated Q212L + D280N) protein
    See all GNAS proteins and peptides
  • Expression system

    Baculovirus infected Sf9 cells
  • Protein length

    Full length protein
  • Animal free

    No
  • Nature

    Recombinant
    • Species

      Rat

Specifications

Our Abpromise guarantee covers the use of ab90410 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • Applications

    Functional Studies

  • Form

    Liquid
  • Additional notes


    In contrast to all other known G protein alpha D/N mutants, the exchange of Asp280 to Asn280 in GGsalphaS does not lead to an inactivation in nucleotide binding. Mutation of Gln212 to Leu212 inhibits the intrinsic GTPase activity, resulting in a constitutively activated GsalphaS. This mutation also increases the GDP-affinity of GsalphaS.

  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 7.40
    Constituents: 0.11875% Magnesium chloride, 1.185% Tris HCl, 0.0292% EDTA

General Info

  • Alternative names

    • Adenylate cyclase stimulating G alpha protein
    • AHO
    • Alternative gene product encoded by XL exon
    • C20orf45
    • dJ309F20.1.1
    • dJ806M20.3.3
    • Extra large alphas protein
    • GNAS
    • GNAS complex locus
    • GNAS1
    • GPSA
    • Gs alpha subunit
    • GSA
    • GSP
    • Guanine nucleotide binding protein (G protein) alpha stimulating activity polypeptide 1
    • Guanine nucleotide binding protein alpha stimulating activity polypeptide 1
    • Guanine nucleotide binding protein G(s) subunit alpha isoforms short
    • Guanine nucleotide binding protein G(s) subunit alpha isoforms XLas
    • Guanine nucleotide regulatory protein
    • MGC33735
    • NESP
    • NESP55
    • Neuroendocrine secretory protein
    • PHP1A
    • PHP1B
    • PHP1C
    • POH
    • Protein ALEX
    • Protein GNAS
    • Protein NESP55
    • SCG6
    • Secretogranin VI
    • XLalphas
    • XLas
    see all
  • Relevance

    Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. The Gs protein is involved in hormonal regulation of adenylate cyclase: it activates the cyclase in response to beta-adrenergic stimuli. Alternative splicing of downstream exons of the GNAS gene is observed, which results in different forms of the stimulatory G protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Multiple transcript variants have been found for this gene, but the full-length nature and/or biological validity of some variants have not been determined. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors.
  • Cellular localization

    Cell Membrane

Protocols

To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

Click here to view the general protocols

Datasheets and documents

    • Datasheet
  • References (0)

    Publishing research using ab90410? Please let us know so that we can cite the reference in this datasheet.

    ab90410 has not yet been referenced specifically in any publications.

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