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PDCD10 antibody (AA 1-212)

This anti-PDCD10 antibody is a Rabbit Polyclonal antibody detecting PDCD10 in WB and ELISA. Suitable for Human, Rat and Mouse.
Catalog No. ABIN6654194

Quick Overview for PDCD10 antibody (AA 1-212) (ABIN6654194)

Target

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

Reactivity

Human, Rat, Mouse

Host

  • 55
  • 2
Rabbit

Clonality

  • 55
  • 2
Polyclonal

Conjugate

  • 19
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PDCD10 antibody is un-conjugated

Application

  • 21
  • 20
  • 13
  • 13
  • 6
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 15
    • 10
    • 7
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-212

    Purification

    Antigen affinity purified

    Immunogen

    Human PDCD10 recombinant protein (amino acids M1-A212) was used as the immunogen for the PDCD10 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the PDCD10 antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL,Direct ELISA: 0.1-0.5 μg/mL (human recombinant protein)

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    -20 °C

    Storage Comment

    After reconstitution, the PDCD10 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    PDCD10 (Programmed Cell Death 10 (PDCD10))

    Alternative Name

    PDCD10

    Background

    Programmed cell death protein 10 is a protein that in humans is encoded by the PDCD10 gene. This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified.

    UniProt

    Q9BUL8
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