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VRK1 Protein

This Recombinant VRK1 protein is expressed in Baculovirus infected Insect Cells.
Catalog No. ABIN7317539

Quick Overview for VRK1 Protein (ABIN7317539)

Target

See all VRK1 Proteins
VRK1 (Vaccinia Related Kinase 1 (VRK1))

Protein Type

Recombinant

Origin

  • 6
  • 1
  • 1
Human

Source

  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Baculovirus infected Insect Cells

Purity

> 95 % as determined by reducing SDS-PAGE.
  • Purpose

    Recombinant Human VRK1 Protein

    Sequence

    Met 1-Lys 396

    Characteristics

    A DNA sequence encoding the human VRK1 (Q99986) (Met 1-Lys 396) was expressed and purified with two additional amino acids (Gly & Pro ) at the N-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 sterile 20 mM Tris, 500 mM NaCl, 10 % glycerol, 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

    VRK1 (Vaccinia Related Kinase 1 (VRK1))

    Alternative Name

    VRK1

    Background

    Background: VRK1 is a member of the vaccinia-related kinase (VRK) family of serine/threonine protein kinases. Serine/threonine protein kinases are tumor suppressor that controls the activity of AMP-activated protein kinase family members, thereby playing a role in various processes such as cell metabolism, cell polarity, apoptosis and DNA damage response. VRK1 contains 1 protein kinase domain and localizes to the nucleus. VRK1 gene is widely expressed in human tissues and has increased expression in actively dividing cells, such as those in testis, thymus, fetal liver, and carcinomas. As a serine/threonine kinase, VRK1 phosphorylates 'Thr-18' of p53/TP53 and may thereby prevent the interaction between p53/TP53 and MDM2. Defects in VRK1 are the cause of pontocerebellar hypoplasia type 1 (PCH1), also called pontocerebellar hypoplasia with infantile spinal muscular atrophy or pontocerebellar hypoplasia with anterior horn cell disease. PCH1 is characterized by an abnormally small cerebellum and brainstem, central and peripheral motor dysfunction from birth, gliosis and anterior horn cell degeneration resembling infantile spinal muscular atrophy.

    Synonym: PCH1,PCH1A

    Molecular Weight

    45.6 kDa

    UniProt

    Q99986
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