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ATP13A2 antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects ATP13A2 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5530316

Quick Overview for ATP13A2 antibody (C-Term) (ABIN5530316)

Target

See all ATP13A2 Antibodies
ATP13A2 (ATPase Type 13A2 (ATP13A2))

Reactivity

  • 20
  • 18
  • 4
  • 1
Human

Host

  • 32
  • 3
Rabbit

Clonality

  • 33
  • 2
Polyclonal

Conjugate

  • 14
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ATP13A2 antibody is un-conjugated

Application

  • 15
  • 14
  • 13
  • 13
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 5
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1133-1161, C-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This ATP13A2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1133-1161 amino acids from the C-terminal region of human ATP13A2.

    Isotype

    Ig Fraction
  • Application Notes

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) 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 for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    ATP13A2 (ATPase Type 13A2 (ATP13A2))

    Alternative Name

    ATP13A2

    Background

    This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    129 kDa

    Gene ID

    23400

    UniProt

    Q9NQ11

    Pathways

    Ribonucleoside Biosynthetic Process
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