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PDCD10 Protein (His tag)

This Recombinant PDCD10 protein is expressed in Escherichia coli (E. coli).
Catalog No. ABIN1589742

Quick Overview for PDCD10 Protein (His tag) (ABIN1589742)

Target

See all PDCD10 Proteins
PDCD10 (Programmed Cell Death 10 (PDCD10))

Protein Type

Recombinant

Origin

  • 7
  • 2
  • 1
Human

Source

  • 3
  • 3
  • 2
  • 1
  • 1
Escherichia coli (E. coli)

Purity

> 95 % by SDS-PAGE
  • Purification tag / Conjugate

    This PDCD10 protein is labelled with His tag.

    Purpose

    CCM-3

    Sequence

    MGSSHHHHHH SSGLVPRGSM RMTMEEMKNE AETTSMVSMP LYAVMYPVFN ELERVNLSAA QTLRAAFIKA EKENPGLTQD IIMKILEKKS VEVNFTESLL RMAADDVEEY MIERPEPEFQ DLNEKARALK QILSKIPDEI NDRVRFLQTI KDIASAIKEL LDTVNNVFKK YQYQNRRALE HQKKEFVKYS KSFSDTLKTY FKDGKAINVF VSANRLIHQT NLILQTFKTV A

    Specificity

    Chromosomal location:3q26.1

    Characteristics

    Length (aa):231
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    Product
    Expression System
    Conjugate
    Origin
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    Expression System HEK-293 Cells
    Conjugate His tag
    Origin Human
    Price starts at $12,595.45
    Expression System Cell-free protein synthesis (CFPS)
    Conjugate Strep Tag
    Origin Human
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  • Comment

    Cytokines & Growth Factors

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    The lyophilized CCM3 is soluble in water and most aqueous buffers and should be reconstituted in water or PBS.

    Buffer

    PBS

    Storage

    -20 °C,-80 °C

    Storage Comment

    Lyophilized samples are stable for greater than six months at -20°C to -70°C. Reconstituted CCM-3 should be stored in working aliquots at -20°C.

    Expiry Date

    6 months
  • Target

    PDCD10 (Programmed Cell Death 10 (PDCD10))

    Alternative Name

    CCM-3

    Background

    Cerebral cavernous malformations (CCMs) are sporadically acquired or inherited vascular lesions of the central nervous system consisting of clusters of dilated thin-walled blood vessels that predispose individuals to seizures and stroke. Mutations in CCM1, CCM2, or CCM3 lead to cerebral cavernous malformations, one of the most common hereditary vascular diseases of the brain. Endothelial cells within these lesions are the main disease compartments. Here, we show that adenoviral CCM3 expression inhibits endothelial cell migration, proliferation, and tube formation while down regulation of endogenous CCM3 results in increased formation of tube-like structures. Adenoviral CCM3 expression does not induce apoptosis under normal endothelial cell culture conditions but protects endothelial cells from staurosporine-induced cell death. Tyrosine kinase activity profiling suggests that CCM3 supports PDPK-1/Akt-mediated endothelial cell quiescence and survival (Schleider et al, Neurogenetics 12, 2011). The CCM-3 is fused to a N-terminal His-tag (6x His).
    Synonyms: PDCD10, CCM3, TFAR15, programmed cell death 10

    Molecular Weight

    26.7 kDa

    Gene ID

    11235

    NCBI Accession

    NM_007217, NP_009148

    UniProt

    Q9BUL8
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