TPP1 anticorps (AA 284-563)

N° du produit ABIN6149442

Détail du produit anti-TPP1 anticorps

Antigène: TPP1 (Tripeptidyl Peptidase I (TPP1))

Épitope: AA 284-563

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TPP1 est non-conjugé

Application: Western Blotting (WB)

Séquence: GANISTWVYS SPGRHEGQEP FLQWLMLLSN ESALPHVHTV SYGDDEDSLS SAYIQRVNTE LMKAAARGLT LLFASGDSGA GCWSVSGRHQ FRPTFPASSP YVTTVGGTSF QEPFLITNEI VDYISGGGFS NVFPRPSYQE EAVTKFLSSS PHLPPSSYFN ASGRAYPDVA ALSDGYWVVS NRVPIPWVSG TSASTPVFGG ILSLINEHRI LSGRPPLGFL NPRLYQQHGA GLFDVTRGCH ESCLDEEVEG QGFCSGPGWD PVTGWGTPNF PALLKTLLNP

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 284-563 of human TPP1 (NP_000382.3).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur TPP1

Antigène: TPP1 (Tripeptidyl Peptidase I (TPP1))

Autre désignation: TPP1 (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: 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.,TPP1,CLN2,GIG1,LPIC,SCAR7,TPP-1,Cell Biology & Developmental Biology,Ubiquitin,Neuroscience,Neurodegenerative Diseases,TPP1

Poids moléculaire: 34 kDa/61 kDa

ID gène: 1200

UniProt: O14773

Pathways: Cycle Cellulaire, ER-Nucleus Signaling