TPP1 Antikörper (AA 66-294)

Produktnummer ABIN1886604

Produktdetails anti-TPP1 Antikörper

Target: TPP1 (Tripeptidyl Peptidase I (TPP1))

Bindungsspezifität: AA 66-294

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TPP1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Aufreinigung: 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

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Thimerosal (Merthiolate)

Vorsichtsmaßnahmen: Biohazard Informations: This product contains thimerosal which is hazardous.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Details zu TPP1

Target: TPP1 (Tripeptidyl Peptidase I (TPP1))

Andere Bezeichnung: CLN2 (TPP1 Produkte)

Synonyme: cln2 antikoerper, fa01b09 antikoerper, im:7149243 antikoerper, wu:fa01b09 antikoerper, CLN2 antikoerper, LPIC antikoerper, TPP-1 antikoerper, TPP-I antikoerper, Cln2 antikoerper, tripeptidyl peptidase I antikoerper, tripeptidyl-peptidase 1 antikoerper, tripeptidyl peptidase 1 antikoerper, tpp1 antikoerper, NAEGRDRAFT_78259 antikoerper, MCYG_00184 antikoerper, MGYG_05881 antikoerper, MGYG_00757 antikoerper, TPP1 antikoerper, Tpp1 antikoerper

Hintergrund: 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]

Molekulargewicht: 61 kDa

Gen-ID: 1200

Pathways: Zellzyklus, ER-Nucleus Signaling