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PINK1 antibody (AA 493-526)

This anti-PINK1 antibody is a Rabbit Polyclonal antibody detecting PINK1 in WB and ELISA. Suitable for Human and Mouse.
Catalog No. ABIN3032403

Quick Overview for PINK1 antibody (AA 493-526) (ABIN3032403)

Target

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

Reactivity

  • 82
  • 27
  • 10
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 55
  • 35
  • 1
Rabbit

Clonality

  • 59
  • 34
Polyclonal

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

  • 71
  • 51
  • 42
  • 20
  • 20
  • 6
  • 6
  • 6
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 22
    • 8
    • 7
    • 6
    • 5
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 493-526

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 493-526 from the human protein was used as the immunogen for this PINK1 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the PINK1 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 PINK1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    PINK1 (PTEN Induced Putative Kinase 1 (PINK1))

    Alternative Name

    PINK1

    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. The mutation is the most common cause of Parkinson disease identified to date. Defects in PINK1 are the cause of autosomal recessive early-onset Parkinson's disease 6 (PARK6). Six novel pathogenic PINK1 mutations suggest that PINK1 may be the second most common causative gene next to parkin in parkinsonism with the recessive mode of inheritance. 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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