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          • Primary Antibodies ›
          • GBA Antibodies

          Fabgennix

          GBA Polyclonal Antibody

          View all (25) GBA antibodies

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          Cite GBA Polyclonal Antibody

          Additional Information:
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          • Antibody Testing Data (1)
          GBA Antibody in Western Blot (WB)
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          GBA Antibody in Western Blot (WB)
          Group 53 Created with Sketch.

          FIGURE: 1 / 1

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          GBA Antibody (GLCM-101AP) in WB

          Western blot of GBA antibody (GLCM-101AP) with GBA positive control (PC-GLCM). Various quantities of GBA Positive control was used. {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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          GBA Antibody in Western Blot (WB)

          Product Details

          GLCM-101AP

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          1:500-1:1,000
          -

          Immunohistochemistry (IHC)

          1:50-1:250
          -

          ELISA (ELISA)

          1:10,000
          -

          Immunoprecipitation (IP)

          1:50-1:250
          -
          Product Specifications

          Species Reactivity

          Human, Mouse

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          Recombinant Glucosylceramidase protein.

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          0.5-1.5 mg/mL

          Purification

          Affinity chromatography

          Storage buffer

          proprietary buffer, pH 7.4-7.8, with 30% glycerol, 0.5% BSA

          Contains

          0.02% sodium azide

          Storage conditions

          -20°C

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          Target Information

          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.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          References (0)

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          Cite this product

          Bioinformatics

          Protein Aliases: acid beta glucosidase; Acid beta-glucosidase; Alglucerase; Beta-GC; Beta-glucocerebrosidase; Beta-glucosylceramidase 1; Cholesterol glucosyltransferase; Cholesteryl-beta-glucosidase; D-glucosyl-N-acylsphingosine glucohydrolase; glucocerebrosidase; glucocerebrosidase precursor (5' end put.); putative; glucosidase, beta, acid; glucosylceramidase; Glucosylceramidase beta 1; glucosylceramidase-like protein; Imiglucerase; Lysosomal acid GCase; Lysosomal acid glucosylceramidase; Lysosomal cholesterol glycosyltransferase; Lysosomal galactosylceramidase; lysosomal glucocerebrosidase; Lysosomal glycosylceramidase; SGTase; unnamed protein product

          View more View less

          Gene Aliases: betaGC; GBA; GBA1; GC; GCase; GCB; GLUC

          View more View less

          UniProt ID: (Human) P04062, (Mouse) P17439

          View more View less

          Entrez Gene ID: (Human) 2629, (Mouse) 14466

          View more View less

          Function(s)
          galactosylceramidase activity glucosylceramidase activity receptor binding scavenger receptor binding protein binding beta-glucosidase activity transferase activity transferase activity, transferring glycosyl groups hydrolase activity hydrolase activity, acting on glycosyl bonds glucosyltransferase activity steryl-beta-glucosidase activity
          Process(es)
          carbohydrate metabolic process lipid metabolic process sphingolipid metabolic process glucosylceramide catabolic process metabolic process response to pH termination of signal transduction negative regulation of interleukin-6 production regulation of water loss via skin response to testosterone positive regulation of protein dephosphorylation negative regulation of MAP kinase activity skin morphogenesis response to estrogen sphingosine biosynthetic process ceramide biosynthetic process response to glucocorticoid cellular response to tumor necrosis factor response to thyroid hormone positive regulation of proteolysis involved in cellular protein catabolic process mitophagy glucosylceramide metabolic process autophagy mitochondrion organization lysosome organization central nervous system development steroid metabolic process cholesterol metabolic process determination of adult lifespan cellular response to starvation negative regulation of macromolecule metabolic process microglia differentiation regulation of macroautophagy antigen processing and presentation lipid storage cerebellar Purkinje cell layer formation pyramidal neuron differentiation respiratory electron transport chain lipid glycosylation neuron projection development negative regulation of protein complex assembly regulation of TOR signaling positive regulation of proteasomal ubiquitin-dependent protein catabolic process T cell differentiation in thymus regulation of protein catabolic process regulation of membrane potential proteasome-mediated ubiquitin-dependent protein catabolic process negative regulation of MAPK cascade negative regulation of neuron apoptotic process cell maturation brain morphogenesis homeostasis of number of cells negative regulation of inflammatory response neurological system process neuromuscular process regulation of protein metabolic process positive regulation of protein metabolic process negative regulation of protein metabolic process neuron apoptotic process establishment of skin barrier microglial cell proliferation motor behavior hematopoietic stem cell proliferation response to dexamethasone lymphocyte migration skin epidermis development beta-glucoside catabolic process positive regulation of neuronal action potential autophagosome organization positive regulation of type 2 mitophagy lysosomal protein catabolic process regulation of lysosomal protein catabolic process
          It has to be done as per old AB suggested Products section.

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