Invitrogen™ GBA Monoclonal Antibody (660CT8.6.6.2)

Mouse Monoclonal Antibody

Supplier:  Invitrogen™ MA537615

Catalog No. PIMA537615

Description

GBA Monoclonal Antibody for Western Blot

GBA 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.

Specifications

• Antigen: GBA
• Classification: Monoclonal
• Concentration: Conc. Not Determined
• Formulation: ascites with 0.09% sodium azide; pH 7.4
• Gene Accession No.: P04062
• Gene Symbols: GBA
• Immunogen: KLH conjugated synthetic peptide between 337-365 amino acids from the Central region of human GC.
• Regulatory Status: RUO
• Gene ID (Entrez): 2629
• Content And Storage: Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
• Form: Liquid

• Applications: Western Blot
• Clone: 660CT8.6.6.2
• Conjugate: Unconjugated
• Gene: GBA
• Gene Alias: acid beta glucosidase; acid beta-glucosidase; Alglucerase; betaGC; beta-GC; Beta-glucocerebrosidase; Cholesterol glucosyltransferase; Cholesteryl-beta-glucosidase; D-glucosyl-N-acylsphingosine glucohydrolase; Gba; GBA1; GBAP; GBAP1; GC; GCase; GCB; GLUC; glucocerebrosidase; glucosidase, beta, acid; glucosylceramidase; glucosylceramidase beta; glucosylceramidase beta pseudogene 1; glucosylceramidase-like protein; imiglucerase; Lysosomal acid GCase; Lysosomal acid glucosylceramidase; lysosomal glucocerebrosidase; SGTase
• Host Species: Mouse
• Quantity: 100 μL
• Primary or Secondary: Primary
• Target Species: Human
• Product Type: Antibody
• Isotype: IgM