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GBA2 Antibody (Biotin)

CAT: 0013-GTR17907346-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR17907346-01Size:50 µg
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Description
This GBA2 Antibody, Biotin conjugated is an Biotin polyclonal product. It tagets GBA2 using a Recombinant Human Non-lysosomal glucosylceramidase protein (656-867AA) as the immunogen. This antibody is suitable for ELISA. Purification: >95%, Protein G purified.
Product Name Alternative
GBA2 antibody; KIAA1605 antibody; SPG46 antibody; AD035Non-lysosomal glucosylceramidase antibody; NLGase antibody; EC 3.2.1.45 antibody; Beta-glucocerebrosidase 2 antibody; Beta-glucosidase 2 antibody; Bile acid beta-glucosidase GBA2 antibody; Bile acid glucosyl transferase GBA2 antibody; Cholesterol glucosyltransferase GBA2 antibody; EC 2.4.1.- antibody; Cholesteryl-beta-glucosidase GBA2 antibody; EC 3.2.1.104 antibody; Glucosylceramidase 2 antibody
UniProt
Q9HCG7
Reactivity
Human
Immunogen
Recombinant Human Non-lysosomal glucosylceramidase protein (656-867AA)
Target
GBA2
Clonality
Polyclonal
Conjugation
Biotin
Field of Research
Metabolism Research
Purification
>95%, Protein G purified
Dilution
ELISA
Form
Liquid
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Notes
For research use only.
Tested Applications
ELISA
Host or Source
Rabbit
Preservative
Preservative: 0.03% Proclin 300. Constituents: 50% Glycerol
Isotype
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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