GBA antibody (clone 200), anti-human
€435.00
In stock
SKU
AC-AT2167a
Catalog Number: AC-AT2167a
Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB, IHC, IF, E
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Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB, IHC, IF, E
Request Information AC-AT2167a">Request Information
Background:
This gene 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.
Other Names:
Glucosylceramidase, Acid beta-glucosidase, Alglucerase, Beta-glucocerebrosidase, Beta-GC, D-glucosyl-N-acylsphingosine glucohydrolase, Imiglucerase, GBA, GC, GLUC
Antigen Type:
Recombinant Protein
Gene Name: GBA1 (HGNC:4177)
Gene ID: 2629
NCBI Accession: NP_000148.2;NP_001005741.1;NP_001005742.1
Primary Accession: P04062
Other Accession: NM_000157
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
This gene 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.
Other Names:
Glucosylceramidase, Acid beta-glucosidase, Alglucerase, Beta-glucocerebrosidase, Beta-GC, D-glucosyl-N-acylsphingosine glucohydrolase, Imiglucerase, GBA, GC, GLUC
Antigen Type:
Recombinant Protein
Gene Name: GBA1 (HGNC:4177)
Gene ID: 2629
NCBI Accession: NP_000148.2;NP_001005741.1;NP_001005742.1
Primary Accession: P04062
Other Accession: NM_000157
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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