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Recombinant Human TPP1/CLN2 Protein (His Tag)(Active) - PKSH030613Recombinant Human TPP1 CLN2 Protein (His Tag)(Active) Size: 50g Catalogue Number: PKSH030613 50 Citations, Manuals and MSDS Available upon request. Abbreviation: TPP1; CLN2 Target Symptom: Tripeptidyl Peptidase 1; TPP 1; Cell Growth Inhibiting Gene 1 Protein; Lysosomal Pepstatin Insensitive Protease; LPIC; Tripeptidyl Aminopeptidase; TPP1; CLN2; GIG1; LPIC; SCAR7; TPP 1 Target Species: Human Expression Host: Baculovirus Insect Cells Application:
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Recombinant Human TPP1/CLN2 Protein (His Tag)(Active)

Size: 50μg

Catalogue Number: PKSH030613-50

Citations, Manuals and MSDS Available upon request.

Abbreviation: TPP1; CLN2

Target Symptom: Tripeptidyl-Peptidase 1; TPP-1; Cell Growth-Inhibiting Gene 1 Protein; Lysosomal Pepstatin-Insensitive Protease; LPIC; Tripeptidyl Aminopeptidase; TPP1; CLN2; GIG1; LPIC; SCAR7; TPP-1

Target Species: Human

Expression Host: Baculovirus-Insect Cells

Application: Enzyme

Fusion Tag: C-His

Accession: AAH14863.1

Background: Tripeptidyl-peptidase 1 (TPP1 / CLN2) is 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. TPP1 / CLN2 May act as a non-specific lysosomal peptidase which generates tripeptides from the breakdown products produced by lysosomal proteinases. Defects in TPP1 / CLN2 are the cause of neuronal ceroid lipofuscinosis type 2 (CLN2), a form of neuronal ceroid lipofuscinosis which is associated with the failure to degrade specific neuropeptides and a subunit of ATP synthase in the lysosome. Neuronal ceroid lipofuscinoses are progressive neurodegenerative, lysosomal storage diseases characterized by intracellular accumulation of autofluorescent liposomal material, and clinically by seizures, dementia, visual loss, and/or cerebral atrophy.

Activity: Measured by the cleavage of AlaAlaPheAMC. The specific activity is > 850 pmoles/min/μg.

Sequence: Met 1-Pro 563

Purity: > 95 % as determined by reducing SDS-PAGE.

Formulation: Lyophilized from sterile 20mM Tris, 500mM NaCl, pH 7.4, 10% glycerol
Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.

Reconstitution: Please refer to the printed manual for detailed information.

Endotoxin: < 1.0 EU per μg of the protein as determined by the LAL method.

Calculated MW: 60.7 kDa

Observed MW: 60 kDa

Storage: Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.

Shipping: This product is provided as lyophilized powder which is shipped with ice packs.

Research Use Only

Recombinant Human TPP1/CLN2 Protein (His Tag)(Active) - PKSH030613

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