Glucosidase, beta (Bile Acid) 2 (GBA2) Kits ELISA

GBA2 encodes a microsomal beta-glucosidase that catalyzes the hydrolysis of bile acid 3-O-glucosides as endogenous compounds. De plus, nous expédions GBA2 Anticorps (39) et GBA2 Protéines (5) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
Anti-Souris GBA2 GBA2 230101 Q69ZF3
GBA2 298399  
GBA2 57704 Q9HCG7
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Top GBA2 Kits ELISA sur anticorps-enligne.fr

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Catalogue No. Reactivité Sensibilité Gamme Images Quantité Fournisseur Livraison Prix Détails
Rat 1.875 ng/mL 3.125 ng/mL - 200 ng/mL   96 Tests Connectez-vous pour afficher 11 to 18 Days
$724.89
Détails
Humain < 0.188 ng/mL 0.313 ng/mL - 20 ng/mL   96 Tests Connectez-vous pour afficher 11 to 18 Days
$810.17
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Plus Kits ELISA pour GBA2 partenaires d'interaction

Zebrafish Glucosidase, beta (Bile Acid) 2 (GBA2) interaction partners

  1. These results provide a foundation for the use of zebrafish in screening GBA2-targeting molecules, and for wider studies investigating GBA2 biology.

  2. GBA2 loss of function led to abnormal motor behavior and axonal shortening/branching of motoneurons.

Mouse (Murine) Glucosidase, beta (Bile Acid) 2 (GBA2) interaction partners

  1. sphingosine, the cytotoxic metabolite accumulating in Gaucher cells through the action of GBA2, directly binds to GBA2 and inhibits its activity.

  2. GBA2 is particularly abundant in Purkinje cells (PCs), one of the most affected neuronal populations in NPC (Montrer NPC1 Kits ELISA) disease.

  3. glucosylceramide accumulation in GBA2 knockout-mice alters cytoskeletal dynamics due to a more ordered lipid organization in the plasma membrane. Similar cytoskeletal defects were observed in male germ and Sertoli cells from GBA2 knockout-mice.

  4. the deletion of Gba2 significantly rescues the type 1 Gaucher disease clinical phenotype.

  5. redefine GBA2 activity as the beta-glucosidase that is sensitive to inhibition by N-butyldeoxygalactonojirimycin.

  6. GBA2 is localized at the ER and Golgi, which puts GBA2 in a key position for a lysosome-independent route of glucosylceramide-dependent signaling.

  7. The repression of IL-6 (Montrer IL6 Kits ELISA)/STAT3 (Montrer STAT3 Kits ELISA) signalling pathway seems to be one of the mechanisms for the delay of liver regeneration in GBA2-deficient mice.

  8. GBA1 (Montrer GBA Kits ELISA) and GBA2 activities had characteristic differences between the studied fibroblast, liver and brain samples.

  9. The coiled-coil structure of LIMP-2 (Montrer SCARB2 Kits ELISA) is required for its interaction with beta-glucocerebrosidase (Montrer GBA Kits ELISA).

  10. L-type calcium channel blockers have the ex vivo effects of increasing GCase (Montrer GBA Kits ELISA) activity and protein in mouse fibroblasts

Human Glucosidase, beta (Bile Acid) 2 (GBA2) interaction partners

  1. Demonstrate that GBA2 plays a role in the proinflammatory state characterizing cystic fibrosis (Montrer S100A8 Kits ELISA) cells. Report for the first time that Pseudomonas aeruginosa infection causes a recruitment of plasma membrane-associated glycosphingolipid hydrolases into lipid rafts of CuFi-1-infected cells.

  2. Our protocol showed high specificity and sensitivity for homozygosity detection and facilitated the identification of novel mutations in GAN, GBA2, and ZFYVE26 in four families affected by hereditary spastic paraplegia or Charcot-Marie-Tooth disease

  3. GBA (Montrer GBA Kits ELISA) mutations as risk factors for PD and point to lysosomal dysfunction as a mechanism contributing to PD etiology.

  4. GBA2 mutations causing a Marinesco-Sjogren-like syndrome in two Norwegian families, are reported.

  5. Mutagenic analysis of TxGH116 and structural modeling of GBA2 provide a detailed structural and functional rationale for pathogenic missense mutations of GBA2

  6. sphingosine, the cytotoxic metabolite accumulating in Gaucher cells through the action of GBA2, directly binds to GBA2 and inhibits its activity.

  7. Spastic paraplegia/cerebellar ataxia patients have a severe deficit in GBA2 activity, because the GBA2 mutants are intrinsically inactive and/or reduced in amount.

  8. The GBA2 gene shows a low mutation frequency in a general population of complicated hereditary spastic paraparesis

  9. Whole-exome and targeted sequencing have defined the genetic basis of dizziness including new genes causing ataxia: GBA2, TGM6, ANO10 and SYT14

  10. We hereby report a novel GBA2 mutation associated with spastic ataxia and suggest that GBA2 mutations may be a relatively frequent cause of autosomal recessive cerebellar ataxias.

GBA2 profil antigène

Antigen Summary

This gene encodes a microsomal beta-glucosidase that catalyzes the hydrolysis of bile acid 3-O-glucosides as endogenous compounds. Studies to determine subcellular localization of this protein in the liver indicated that the enzyme was mainly enriched in the microsomal fraction where it appeared to be confined to the endoplasmic reticulum. This putative transmembrane protein is thought to play a role in carbohydrate transport and metabolism.

Gene names and symbols associated with GBA2

  • talin 1 (TLN1) anticorps
  • glucosidase, beta (bile acid) 2 (gba2) anticorps
  • glucosylceramidase beta 2 (GBA2) anticorps
  • glucosidase beta 2 (Gba2) anticorps
  • glucosylceramidase beta 2 (Gba2) anticorps
  • F630034E04 anticorps
  • SPG46 anticorps
  • TLN1 anticorps

Protein level used designations for GBA2

bile acid beta-glucosidase , talin 1 , glucosidase, beta (bile acid) 2 , non-lysosomal glucosylceramidase-like , NLGase , beta-glucocerebrosidase 2 , beta-glucosidase 2 , bile acid , glucosylceramidase 2 , non-lysosomal glucosylceramidase

GENE ID SPECIES
465082 Pan troglodytes
559240 Danio rerio
696062 Macaca mulatta
100145361 Xenopus (Silurana) tropicalis
100438148 Pongo abelii
100476888 Ailuropoda melanoleuca
230101 Mus musculus
298399 Rattus norvegicus
57704 Homo sapiens
100859407 Gallus gallus
474760 Canis lupus familiaris
100155655 Sus scrofa
100139170 Bos taurus
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