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PINK1 antibody (AA 237-266)

The Rabbit Polyclonal anti-PINK1 antibody has been validated for WB and ELISA. It is suitable to detect PINK1 in samples from Human and Mouse.
Catalog No. ABIN3028955

Quick Overview for PINK1 antibody (AA 237-266) (ABIN3028955)

Target

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

Reactivity

  • 89
  • 28
  • 10
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 57
  • 44
  • 1
Rabbit

Clonality

  • 61
  • 43
Polyclonal

Conjugate

  • 58
  • 8
  • 6
  • 5
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PINK1 antibody is un-conjugated

Application

  • 77
  • 62
  • 43
  • 28
  • 20
  • 8
  • 6
  • 6
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 28
    • 8
    • 7
    • 6
    • 6
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 237-266

    Purification

    Purified

    Immunogen

    A portion of amino acids 237-266 from human PINK1 was used as the immunogen for this PINK antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the PINK antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % 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

    -20 °C

    Storage Comment

    Aliquot the PINK antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    PINK1 (PTEN Induced Putative Kinase 1 (PINK1))

    Alternative Name

    PINK

    Background

    Parkinson is the second most common neurodegenerative disease after Alzheimers. About 1 percent of people over the age of 65 and 3 percent of people over the age of 75 are affected by the disease. Defects in PINK1 are the cause of autosomal recessive early-onset Parkinson's disease 6 (PARK6). Strong evidence indicates that, although important in mendelian forms of Parkinson's disease (PD), PINK1 does not influence the cause of sporadic nonmendelian forms of PD.

    UniProt

    Q9BXM7

    Pathways

    Autophagy
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