TPP1 anticorps (AA 66-294)
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- Antigène Voir toutes TPP1 Anticorps
- TPP1 (Tripeptidyl Peptidase I (TPP1))
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Épitope
- AA 66-294
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp TPP1 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
- Purification
- Purified by antigen-affinity chromatography.
- Immunogène
- Recombinant protein fragment contain a sequence corresponding to a region within amino acids 66 and 294 of human TPP1
- Top Product
- Discover our top product TPP1 Anticorps primaire
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- Indications d'application
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Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.250
Immunofluorescence: 1.100-1.200 - Restrictions
- For Research Use only
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- 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.
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- Antigène
- TPP1 (Tripeptidyl Peptidase I (TPP1))
- Autre désignation
- CLN2 (TPP1 Produits)
- Synonymes
- anticorps cln2, anticorps fa01b09, anticorps im:7149243, anticorps wu:fa01b09, anticorps CLN2, anticorps LPIC, anticorps TPP-1, anticorps TPP-I, anticorps Cln2, anticorps tripeptidyl peptidase I, anticorps tripeptidyl-peptidase 1, anticorps tripeptidyl peptidase 1, anticorps tpp1, anticorps NAEGRDRAFT_78259, anticorps MCYG_00184, anticorps MGYG_05881, anticorps MGYG_00757, anticorps TPP1, anticorps Tpp1
- Sujet
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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
- Pathways
- Cycle Cellulaire, ER-Nucleus Signaling
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