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TPP1 anticorps (AA 224-562)

Cet anticorps anti-TPP1 est un anticorps Lapin Polyclonal détectant TPP1 dans WB. Adapté pour Humain.
N° du produit ABIN1886223

Aperçu rapide pour TPP1 anticorps (AA 224-562) (ABIN1886223)

Antigène

Voir toutes TPP1 Anticorps
TPP1 (Tripeptidyl Peptidase I (TPP1))

Reactivité

  • 63
  • 26
  • 11
Humain

Hôte

  • 57
  • 6
  • 1
Lapin

Clonalité

  • 59
  • 5
Polyclonal

Conjugué

  • 31
  • 5
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TPP1 est non-conjugé

Application

  • 49
  • 22
  • 13
  • 13
  • 11
  • 8
  • 7
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 9
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 224-562

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 224 and 562 of CLN2
  • Indications d'application

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    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.

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Stock

    4 °C/-20 °C

    Stockage commentaire

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

    TPP1 (Tripeptidyl Peptidase I (TPP1))

    Autre désignation

    CLN2

    Sujet

    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]

    Poids moléculaire

    61 kDa

    ID gène

    1200

    NCBI Accession

    NP_000382, NM_000391

    Pathways

    Cycle Cellulaire, ER-Nucleus Signaling
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