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PDCD10 antibody

This anti-PDCD10 antibody is a Rabbit Polyclonal antibody detecting PDCD10 in WB and IF. Suitable for Human and Mouse.
Catalog No. ABIN6989859

Quick Overview for PDCD10 antibody (ABIN6989859)

Target

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

Reactivity

  • 40
  • 27
  • 12
Human, Mouse

Host

  • 53
  • 2
Rabbit

Clonality

  • 53
  • 2
Polyclonal

Conjugate

  • 17
  • 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

  • 20
  • 19
  • 13
  • 13
  • 5
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Cross-Reactivity

    Human, Mouse

    Purification

    Purified by Protein A.

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-212 of human PDCD10 (NP_009148.2).

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    IF()

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C for 12 months.

    Expiry Date

    12 months
  • Target

    PDCD10 (Programmed Cell Death 10 (PDCD10))

    Alternative Name

    PDCD10

    Background

    Synonyms: PDCD10,CCM3,TFAR15

    Background: 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.

    Gene ID

    11235

    UniProt

    Q9BUL8
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