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Human GBA / Glucosidase Beta Acid Recombinant (GST) Protein LS-G28588

Ordering

Wt. Vol. Conc. Price
10 µg - - $415
Inquire for larger quantities
LSBio (USA Sales Only) LSBio (USA Sales Only)
206-374-1102
866-206-6909
Orders@LSBio.com
 

Most Popular GBA / Glucosidase Beta Acid Proteins

Human GBA / Glucosidase Beta Acid Recombinant (His) Protein - LS-G14960
E. coli Expression System
His
Unpurified
Human GBA / Glucosidase Beta Acid Recombinant (His) Protein - LS-G14962
E. coli Expression System
His
Unpurified
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Rat GBA / Glucosidase Beta Acid Recombinant (His + GST) Protein - LS-G14965
E. coli Expression System
His + GST
Unpurified
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image

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LS-G28588
Recombinant Protein
GBA / Glucosidase Beta Acid
Human
84.7 kDa
MEFSSPSREE CPKPLSRVSI IAGSLTGLLL LQAVSWASGA
RPCIPKSFGY SSVVCVCNAT YCDSFDPPTF PALGTFSRYE
STRSGRRMEL SMGPIQANHT GTGLLLTLQP EQKFQKVKGF
GGAMTDAAAL NILALSPPAQ NLLLKSYFSE EGIGYNIIRV
PMASCDFSIR TYTYADTPDD FQLHNFSLPE EDTKLKIPLI
HRALQLAQRP VSLLASPWTS PTWLKTNGAV NGKGSLKGQP
GDIYHQTWAR YFVKFLDAYA EHKLQFWAVT AENEPSAGLL
SGYPFQCLGF TPEHQRDFIA RDLGPTLANS THHNVRLLML
DDQRLLLPHW AKVVLTDPEA AKYVHGIAVH WYLDFLAPAK
ATLGETHRLF PNTMLFASEA CVGSKFWEQS VRLGSWDRGM
QYSHSIITNL LYHVVGWTDW NLALNPEGGP NWVRNFVDSP
IIVDITKDTF YKQPMFYHLG HFSKFIPEGS QRVGLVASQK
NDLDAVALMH PDGSAVVVVL NRSSKDVPLT IKDPAVGFLE
TISPGYSIHT YLWRRQ
Wheat Germ Extract
Wheat
GST
Glutathione Sepharose
50 mM Tris-HCl, pH 8.0, 10 mM reduced glutathione
Store at -80°C. Avoid freeze-thaw cycles.
For research use only.

About GBA / Glucosidase Beta Acid

P04062 NM_000157 NP_000148.2

GBA Protein, Acid beta-glucosidase Protein, Alglucerase Protein, Beta-glucocerebrosidase Protein, GBA1 Protein, Glucosidase, beta, acid Protein, GLUC Protein, GCB Protein, Lysosomal glucocerebrosidase Protein, Metaxin Protein, MTXN Protein, Glucosylceramidase Protein, Imiglucerase Protein

GBA / Glucosidase Beta Acid encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.

Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis

Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis
12.5% SDS-PAGE of human GBA stained with Coomassie Blue
 

Requested From: United States
Date Requested: 12/10/2016

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