GBA/glucocerebrosidase, His, Human

GBA/glucocerebrosidase, His, Human

Glucocerebrosidase (GBA) mutations are the most important genetic risk factor for the development of Parkinson disease (PD). GBA encodes the lysosomal enzyme glucocerebrosidase (GCase).
Z05334
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Product Introduction
Species Human
Protein Construction
GBA/glucocerebrosidase (Ala40-Gln536)
Accession # NP_000148.2
His
N-term C-term
Purity > 95% as determined by Bis­Tris PAGE 
> 95% as determined by HPLC
Endotoxin Level Less than 1EU per μg by the LAL method.
Biological Activity Measured by its ability to hydrolyze 4­methylumbelliferyl­beta­D­glucopyranoside. The specific activity is >200 pmol/min/μg. Test result meets the standard.
Expression System HEK293
Theoretical Molecular Weight 56.69 kDa
Apparent Molecular Weight Due to glycosylation, the protein migrates to 60-70 kDa based on Bis-Tris PAGE result.
Formulation Lyophilized from 0.22 μm filtered solution in PBS (pH 7.4).
Reconstitution Centrifuge the tube before opening. Reconstituting to a concentration more than 100 μg/ml is recommended. Dissolve the lyophilized protein in distilled water.
Storage & Stability Upon receiving, the product remains stable up to 6 months at -20 °C or below. Upon reconstitution, the product should be stable for 3 months at -80 °C. Avoid repeated freeze-thaw cycles.

Background
Target Background Glucocerebrosidase (GBA) mutations are the most important genetic risk factor for the development of Parkinson disease (PD). GBA encodes the lysosomal enzyme glucocerebrosidase (GCase).
Synonyms GBA; glucocerebrosidase; Alglucerase; Beta-GC; SGTase; GC; GLUC

For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use.