Recombinant Human Natriuretic Peptide Receptor B protein (ab114435)

製品の概要

製品の詳細

  • 由来Recombinant
  • 由来Wheat germ
  • アミノ酸配列
    • アクセッション番号P20594
    • 生物種Human
    • 配列AKNDHYRTLVRTGPSAPKLGEFVVTLHGHFNWTARAALLYLDARTDDRPH YFTIEGVFEALQGSNLSVQHQVYAREPGGPEQATHFIRANGRIVYICGPL
    • 分子量37 kDa including tags
    • 領域131 to 230

特性

Our Abpromise guarantee covers the use of ab114435 in the following tested applications.

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

  • アプリケーション

    ELISA

    SDS-PAGE

    Western blot

  • 製品の状態Liquid
  • 備考Protein concentration is above or equal to 0.05 mg/ml.
    Best use within three months from the date of receipt of this protein.
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

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

    pH: 8.00
    Constituents: 0.3% Glutathione, 0.79% Tris HCl

関連情報

  • 別名
    • AMDM
    • ANP-B
    • ANPB
    • ANPR-B
    • ANPRB
    • ANPRB_HUMAN
    • Atrial natriuretic peptide B type receptor
    • Atrial natriuretic peptide receptor 2
    • Atrial natriuretic peptide receptor type B
    • Atrionatriuretic peptide receptor B
    • GC-B
    • GCB
    • Guanylate cyclase B
    • GUC 2B
    • GUC2B
    • GUCY2B
    • Natriuretic peptide receptor B
    • Natriuretic peptide receptor B/guanylate cyclase B
    • NPR-B
    • Npr2
    • NPRB
    • NPRBi
    see all
  • 機能Receptor for the C-type natriuretic peptide NPPC/CNP hormone. Has guanylate cyclase activity upon binding of its ligand. May play a role in the regulation of skeletal growth.
  • 関連疾患Defects in NPR2 are the cause of acromesomelic dysplasia Maroteaux type (AMDM) [MIM:602875]. Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDM is an autosomal recessive form characterized by axial skeletal involvement with wedging of vertebral bodies. In AMDM all skeletal elements are present but show abnormal rates of linear growth.
  • 配列類似性Belongs to the adenylyl cyclase class-4/guanylyl cyclase family.
    Contains 1 guanylate cyclase domain.
    Contains 1 protein kinase domain.
  • 翻訳後修飾Phosphorylation of the protein kinase-like domain is required for full activation by CNP.
  • 細胞内局在Membrane.
  • Information by UniProt

Recombinant Human Natriuretic Peptide Receptor B protein 画像

  • ab114435 analysed on a 12.5% SDS-PAGE gel stained with Coomassie Blue.

Recombinant Human Natriuretic Peptide Receptor B protein (ab114435) 使用論文

ab114435 has not yet been referenced specifically in any publications.

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