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GBA2 Antibody

CAT: 0864-A22865-100ULSize: 100 µLDry Ice: NoHazardous: No
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CAT#:0864-A22865-100ULSize:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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CAS Number
9007-83-4
Gene Aliases
GBA2, KIAA1605, SPG46, AD035Non-lysosomal glucosylceramidase, NLGase, EC 3.2.1.45, Beta-glucocerebrosidase 2, Beta-glucosidase 2, Bile acid beta-glucosidase GBA2, Bile acid glucosyl transferase GBA2, Cholesterol glucosyltransferase GBA2, EC 2.4.1.-, Cholesteryl-beta-glucosidase GBA2, EC 3.2.1.104, Glucosylceramidase 2
UniProt
Q9HCG7
Host
Rabbit
Antigen Species
Human
Reactivity
Human, Mouse, Rat
Target Antigen
Human GBA2
Target
GBA2
Clonality
Polyclonal
Conjugation
Non-conjugated
Applications
ELISA, WB
Field of Research
Signal Transduction
Purification Method
Antigen affinity purified
Form
Liquid
Buffer
PBS, 0.02% sodium azide, 50% glycerol, pH 7.3.
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Fragment
IgG

UniProtKB · Q9HCG7

Non-lysosomal glucosylceramidase

GBA2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9HCG7
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
GBA2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
NLGase
EC number
3.2.1.45
Processing
—
Secondary accessions
D3DRP2, Q5TCV6, Q96A51, Q96LY1, Q96SJ2, Q9H2L8
Protein keywords

Coding sequence diversity

Alternative splicing

Biological process

Cholesterol metabolismLipid metabolismSphingolipid metabolismSteroid metabolismSterol metabolism

Technical term

Direct protein sequencingProteomics identificationReference proteome

Disease

Disease variantHereditary spastic paraplegiaNeurodegeneration

Cellular component

Endoplasmic reticulumGolgi apparatusMembrane

Molecular function

GlycosidaseGlycosyltransferaseHydrolaseTransferase

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