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LAP3 antibody (PE)

This anti-LAP3 antibody is a Rabbit Polyclonal antibody detecting LAP3 in FACS. Suitable for Human, Mouse and Rat.
Catalog No. ABIN2177259

Quick Overview for LAP3 antibody (PE) (ABIN2177259)

Target

See all LAP3 Antibodies
LAP3 (Cytosol Aminopeptidase (LAP3))

Reactivity

  • 38
  • 8
  • 8
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
Human, Mouse, Rat

Host

  • 33
  • 5
Rabbit

Clonality

  • 35
  • 3
Polyclonal

Conjugate

  • 23
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This LAP3 antibody is conjugated to PE

Application

  • 23
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  • 5
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  • 2
  • 1
  • 1
Flow Cytometry (FACS)
  • Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human LAP3

    Isotype

    IgG
  • Application Notes

    FCM: (1:20-100)
    Optimal working dilution should be determined by the investigator.

    Comment

    Exitation/Emission: 480,565nm/578nm

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 100 μg/mL BSA, 50 % glycerol and 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

    Store at 4 °C for 12 months.
  • Target

    LAP3 (Cytosol Aminopeptidase (LAP3))

    Alternative Name

    Lap3

    Background

    LAP3 (leucine aminopeptidase 3), also known as LAPEP or PEPS, is a 519 amino acid protein that localizes to the cytoplasm and belongs to the peptidase M17 family. Existing as a homohexamer, LAP3 uses zinc as a cofactor to catalyze the release of an N-terminal proline from a target peptide and is, therefore, involved in the processing and turnover of intracellular proteins. Multiple isoforms of LAP3 exist due to alternative splicing events. The gene encoding LAP3 maps to human chromosome 4, which houses nearly 6 % of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
    Synonyms: Cytosol aminopeptidase, LAP 3, LAP, LAPEP, Leucine aminopeptidase 3, Leucyl aminopeptidase, PEPS, Peptidase S, Proline aminopeptidase, Prolyl aminopeptidase, AMPL_HUMAN.

    Gene ID

    51056
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