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TPP1 antibody (AA 66-294)

This anti-TPP1 antibody is a Rabbit Polyclonal antibody detecting TPP1 in WB, IHC and IF. Suitable for Human.
Catalog No. ABIN1886604

Quick Overview for TPP1 antibody (AA 66-294) (ABIN1886604)

Target

See all TPP1 Antibodies
TPP1 (Tripeptidyl Peptidase I (TPP1))

Reactivity

  • 64
  • 28
  • 11
Human

Host

  • 60
  • 6
  • 1
Rabbit

Clonality

  • 62
  • 5
Polyclonal

Conjugate

  • 34
  • 5
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TPP1 antibody is un-conjugated

Application

  • 52
  • 22
  • 13
  • 13
  • 13
  • 10
  • 8
  • 7
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 15
    • 9
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    • 1
    AA 66-294

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 66 and 294 of human TPP1
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.250
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    TPP1 (Tripeptidyl Peptidase I (TPP1))

    Alternative Name

    CLN2

    Background

    This gene encodes a member of the sedolisin family of serine proteases.The protease functions in the lysosome to cleave N-terminal tripeptides from substrates, and has weaker endopeptidase activity.It is synthesized as a catalytically-inactive enzyme which is activated and auto-proteolyzed upon acidification.Mutations in this gene result in late-infantile neuronal ceroid lipofuscinosis, which is associated with the failure to degrade specific neuropeptides and a subunit of ATP synthase in the lysosome.[provided by RefSeq]

    Molecular Weight

    61 kDa

    Gene ID

    1200

    Pathways

    Cell Division Cycle, ER-Nucleus Signaling
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