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Recombinant Human Beta-2 adrenergic receptor (ADRB2), Truncated

ACP01351

Number
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Specifications


Cat.No ACP01351 Target NameADRB2
FormLiquid or Lyophilized powderExpression SystemE.coli
Expression Range330-413aaMol Weight23.8 kDa
Protein LengthPartialPurityGreater than 90% as determined by SDS-PAGE.
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP07550
Background Information
  • Uniprot Id

    P07550

  • Target Species

    Human

  • Target Name

    ADRB2

  • Target Full Name

    Beta-2 adrenergic receptor

  • Target Function

    Beta-adrenergic receptors mediate the catecholamine-induced activation of adenylate cyclase through the action of G proteins. The beta-2-adrenergic receptor binds epinephrine with an approximately 30-fold greater affinity than it does norepinephrine.

  • Target Subcellular Location

    Cell membrane; Multi-pass membrane protein. Early endosome. Golgi apparatus.

  • Target Protein Families

    G-protein coupled receptor 1 family, Adrenergic receptor subfamily, ADRB2 sub-subfamily

  • Target Research Area

    Cardiovascular

  • Target Synonyms

    ADRB2; ADRB2R; B2AR; Beta-2 adrenergic receptor; Beta-2 adrenoreceptor; Beta-2 adrenoceptor

  • Target Background

    This gene encodes beta-2-adrenergic receptor which is a member of the G protein-coupled receptor superfamily. This receptor is directly associated with one of its ultimate effectors, the class C L-type calcium channel Ca(V)1.2. This receptor-channel complex also contains a G protein, an adenylyl cyclase, cAMP-dependent kinase, and the counterbalancing phosphatase, PP2A. The assembly of the signaling complex provides a mechanism that ensures specific and rapid signaling by this G protein-coupled receptor. This receptor is also a transcription regulator of the alpha-synuclein gene, and together, both genes are believed to be associated with risk of Parkinson's Disease. This gene is intronless. Different polymorphic forms, point mutations, and/or downregulation of this gene are associated with nocturnal asthma, obesity, type 2 diabetes and cardiovascular disease.

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