GBA Human
目录号 : GP21663Beta-Glucocerebrosidase Human Recombinant
Sample solution is provided at 25 µL, 10mM.
GBA produced in Sf9 Baculovirus cells is a single, glycosylated polypeptide chain containing 503 amino acids (40-536a.a.) and having a molecular mass of 56.4kDa (Molecular size on SDS-PAGE will appear at approximately 50-70kDa).GBA is expressed with a 6 amino acid His tag at C-Terminus and purified by proprietary chromatographic techniques.
Purity | Greater than 80% as determined by SDS-PAGE. | Source | Sf9,Baculovirus cells. |
Phycical Appearance | Sterile Filtered colorless solution. | Shipping Condition | Shipped with Ice Packs. |
Synonyms | Glucosidase; Beta; Acid; D-Glucosyl-N-Acylsphingosine Glucohydrolase; Beta-Glucocerebrosidase; Acid Beta-Glucosidase; Glucosylceramidase; Alglucerase; EC 3.2.1.45; Beta-GC; GLUC; Glucosidase; Beta; Acid (Includes Glucosylceramidase); Glucosylceramidase-Like Protein; Lysosomal Glucocerebrosidase; GBA1; GCB; GC; Glucosylceramidase. | ||
Amino Acid Sequence | ARPCIPKSFG YSSVVCVCNA TYCDSFDPPT FPALGTFSRY ESTRSGRRMELSMGPIQANH TGTGLLLTLQ PEQKFQKVKG FGGAMTDAAA LNILALSPPA QNLLLKSYFS EEGIGYNIIRVPMASCDFSI RTYTYADTPD DFQLHNFSLP EEDTKLKIPL IHRALQLAQR PVSLLASPWTSPTWLKTNGA VNGKGSLKGQ PGDIYHQTWA RYFVKFLDAY AEHKLQFWAVTAENEPSAGL LSGYPFQCLG FTPEHQRDFI ARDLGPTLAN STHHNVRLLM LDDQRLLLPH WAKVVLTDPEAAKYVHGIAV HWYLDFLAPA KATLGETHRL FPNTMLFASE ACVGSKFWEQ SVRLGSWDRGMQYSHSIITN LLYHVVGWTD WNLALNPEGG PNWVRNFVDS PIIVDITKDTFYKQPMFYHL GHFSKFIPEG SQRVGLVASQ KNDLDAVALM HPDGSAVVVV LNRSSKDVPL TIKDPAVGFLETISPGYSIH TYLWRRQHHH HHH. | ||
Stability | Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).Avoid multiple freeze-thaw cycles. | ||
Formulation | GBA protein solution (0.5mg/ml) contains Phosphate Buffered Saline (pH7.4) and 10% glycerol. |
Beta-Glucocerebrosidase, also known as GBA is amember of the glycosylhydrolase 30 family. GBA is a lysosomal enzyme which requires a signal peptidefor transport across the membrane of the rough endoplasmic reticulum as well asglycosylation for transport into lysosomes. Furthermore, Gaucher disease iscaused by a deficiency in the activity of the enzyme glucocerebrosidase.
Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).Avoid multiple freeze-thaw cycles.