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BMPR1A Protein (His tag,Fc Tag)

This Recombinant BMPR1A protein is expressed in Human Cells.
Catalog No. ABIN7318202

Quick Overview for BMPR1A Protein (His tag,Fc Tag) (ABIN7318202)

Target

See all BMPR1A Proteins
BMPR1A (Bone Morphogenetic Protein Receptor 1A (BMPR1A))

Protein Type

Recombinant

Origin

  • 19
  • 5
  • 2
  • 1
  • 1
Human

Source

  • 9
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human Cells

Purity

> 95 % as determined by reducing SDS-PAGE.
  • Purification tag / Conjugate

    This BMPR1A protein is labelled with His tag,Fc Tag.

    Purpose

    Recombinant Human BMPRIA/ALK-3 Protein (Fc & His Tag)

    Sequence

    Gln24-Arg152

    Characteristics

    Recombinant Human Bone Morphogenetic Protein Receptor Type IA/Activin Receptor-like Kinase 3 is produced by our Mammalian expression system and the target gene encoding Gln24-Arg152 is expressed with a Fc, 6His tag at the C-terminus.

    Endotoxin Level

    < 1.0 EU per μg as determined by the LAL method.
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  • Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Please refer to the printed manual for detailed information.

    Buffer

    Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Target

    BMPR1A (Bone Morphogenetic Protein Receptor 1A (BMPR1A))

    Alternative Name

    BMPRIA/ALK-3

    Background

    Background: Bone Morphogenetic Protein Receptor Type-1A (BMPR1A) belongs to the TKL Ser/Thr protein kinase family and TGFB receptor subfamily, including the type I receptors BMPR1A and BMPR1B and the type II receptor BMPR2. BMPR1A is a single-pass type I membrane protein and highly expressed in skeletal muscle. BMPR1A contains one GS domain and one protein protein kinase domain. BMPR1A is necessary for the extracellular matrix depostition by osteoblasts. BMPR1A can activate SMAD transcriptional regulators, binding with ligands. Defects in BMPR1A are a cause of juvenile polyposis syndrome, Cowden disease and hereditary mixed polyposis syndrome 2 (HMPS2).

    Synonym: Bone Morphogenetic Protein Receptor Type-1A, BMP Type-1A Receptor, BMPR-1A, Activin Receptor-Like Kinase 3, ALK-3, Serine/Threonine-Protein Kinase Receptor R5, SKR5, CD292, BMPR1A, ACVRLK3, ALK3,10q23del

    Molecular Weight

    42.1 kDa

    UniProt

    P36894

    Pathways

    Stem Cell Maintenance
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