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Recombinant Human GBA1

CAT: 0710-P1780-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0710-P1780-01Size:50 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Product Name Alternative
Acid beta glucosidase, Alglucerase, Beta glucocerebrosidase, GBA, GBA1, GC, GCB, GLUC, Glucosylceramidase, Imiglucerase
UniProt
P04062
Expression Region
362-512
Host
E.Coli
Tag
N-terminal His-IF2DI Tag
Applications
Western Blot, ELISA
Field of Research
Neuroscience, Metabolism
Purity
Greater than 90% as determined by SDS-PAGE.
Form
Lyophilized powder
Reconstitution
Centrifuge the vial before opening, reconstitute in sterile distilled water to a concentration of 0.1-1 mg/ml by gently pipetting 2-3 times, don't vortex.
Molecular Weight
37.6 kDa
Shipping Conditions
4°C with ice bag
Storage Conditions
The lyophilized protein is stable at -20 °C for up to 1 year. For extended storage, it is recommended to further dilute in working aliquots after reconstitution. The protein solution is stable at ≤ -20 °C for 3 months, or 2-7 days at 2-8 °C under sterile conditions.Avoid repeated freeze/thaw cycle.
Formulation
Lyophilized from a 0.2 μm filtered solution of 10 mM Hepes, 150 mM NaCl with 5% trehalose, pH 7.4.
Organism Species
Human

UniProtKB · P04062

Lysosomal acid glucosylceramidase

GBA1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P04062
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
GBA1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
Lysosomal acid GCase
EC number
3.2.1.45
Processing
Precursor
Secondary accessions
A8K796, B7Z5G2, B7Z6S1, J3KQG4, J3KQK9, Q16545, Q4VX22, Q6I9R6, Q9UMJ8
Protein keywords

Technical term

3D-structureDirect protein sequencingPharmaceuticalProteomics identificationReference proteome

Coding sequence diversity

Alternative initiationAlternative splicing

Biological process

Cholesterol metabolismLipid metabolismSphingolipid metabolismSteroid metabolismSterol metabolism

Disease

Disease variantGaucher diseaseIchthyosisNeurodegenerationParkinson diseaseParkinsonism

PTM

Disulfide bondGlycoprotein

Molecular function

GlycosidaseGlycosyltransferaseHydrolaseTransferase

Cellular component

LysosomeMembrane

Domain

Signal

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