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PINK1 antibody (AA 112-273)

The Mouse Monoclonal anti-PINK1 antibody has been validated for IHC, ELISA and FACS. It is suitable to detect PINK1 in samples from Human.
Catalog No. ABIN7193447

Quick Overview for PINK1 antibody (AA 112-273) (ABIN7193447)

Target

See all PINK1 Antibodies
PINK1 (PTEN Induced Putative Kinase 1 (PINK1))

Reactivity

  • 82
  • 28
  • 10
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 56
  • 34
  • 1
Mouse

Clonality

  • 60
  • 33
Monoclonal

Conjugate

  • 51
  • 8
  • 6
  • 5
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PINK1 antibody is un-conjugated

Application

  • 72
  • 50
  • 42
  • 21
  • 20
  • 6
  • 6
  • 5
  • 5
  • 3
  • 1
  • 1
Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)

Clone

5F2B11
  • Binding Specificity

    • 22
    • 8
    • 7
    • 6
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 112-273

    Purpose

    PINK1 Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human PINK1 (AA: 112-273) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    PINK1 (PTEN Induced Putative Kinase 1 (PINK1))

    Alternative Name

    PINK1

    Background

    This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease.

    Molecular Weight

    62.8 kDa

    UniProt

    Q9BXM7

    Pathways

    Autophagy
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