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Solid+Phase+Extraction
Numéro de catalogue:
(R6830-02)
Fournisseur:
OMEGA BIO-TEK
Description:
RNA-Solv® Reagent est un système à un seul réactif pour isoler l'ARN total des cellules et des tissus. Le réactif, une solution monophasée constituée de phénol et d'isothiocyanate de guanidine, est une modification du procédé d'isolement de l'ARN en une seule étape développé par Chomczynski et Sacchi. L'échantillon est homogénéisé et lysé dans le réactif RNA-Solv® Reagent, qui maintient l'intégrité de l'ARN tout en interférant et dénaturant les RNases endogènes et autres composants cellulaires. L'extraction du lysat avec du chloroforme dénature davantage les protéines et divise le mélange en une phase organique et une phase aqueuse. L'ARN reste exclusivement dans la phase aqueuse, et est ensuite récupéré par isopropanol.
UOM:
1 * 200 mL
Numéro de catalogue:
(BOSSBS-1338R-FITC)
Fournisseur:
Bioss
Description:
Binding of anti-Fx1A to Heymann nephritis antigens (HA) on rat glomerular epithelial cells (GECs) in culture leads to capping and disappearance of antigens from the cell surface. This process may contribute to the formation of glomerular subepithelial immune deposits in vivo. The authors differentially extracted GECs to determine whether HA redistribution is mediated by cytoskeletal components. Observations were made by phase-contrast and immunofluorescence microscopy on primary and passaged GECs in monolayer culture and by spectrofluorimetry on GECs in suspension.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1338R-A680)
Fournisseur:
Bioss
Description:
Binding of anti-Fx1A to Heymann nephritis antigens (HA) on rat glomerular epithelial cells (GECs) in culture leads to capping and disappearance of antigens from the cell surface. This process may contribute to the formation of glomerular subepithelial immune deposits in vivo. The authors differentially extracted GECs to determine whether HA redistribution is mediated by cytoskeletal components. Observations were made by phase-contrast and immunofluorescence microscopy on primary and passaged GECs in monolayer culture and by spectrofluorimetry on GECs in suspension.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1338R-A750)
Fournisseur:
Bioss
Description:
Binding of anti-Fx1A to Heymann nephritis antigens (HA) on rat glomerular epithelial cells (GECs) in culture leads to capping and disappearance of antigens from the cell surface. This process may contribute to the formation of glomerular subepithelial immune deposits in vivo. The authors differentially extracted GECs to determine whether HA redistribution is mediated by cytoskeletal components. Observations were made by phase-contrast and immunofluorescence microscopy on primary and passaged GECs in monolayer culture and by spectrofluorimetry on GECs in suspension.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1338R-HRP)
Fournisseur:
Bioss
Description:
Binding of anti-Fx1A to Heymann nephritis antigens (HA) on rat glomerular epithelial cells (GECs) in culture leads to capping and disappearance of antigens from the cell surface. This process may contribute to the formation of glomerular subepithelial immune deposits in vivo. The authors differentially extracted GECs to determine whether HA redistribution is mediated by cytoskeletal components. Observations were made by phase-contrast and immunofluorescence microscopy on primary and passaged GECs in monolayer culture and by spectrofluorimetry on GECs in suspension.
UOM:
1 * 100 µl
Numéro de catalogue:
(590-0036)
Fournisseur:
VWR Collection
Description:
Extraction des solvants ou des phases mobiles en toute sécurité des flacons et réservoirs sans exposition aux gaz et vapeurs de solvants nocifs. Matériaux de haute qualité (PTFE et PP) garantissant une sécurité optimale pour l'environnement et le personnel de laboratoire.
UOM:
1 * 1 ST
Fournisseur:
LABCONCO
Description:
Solid epoxy work surface, black, 1830 mm width, 63 kg, Pour: —
Numéro de catalogue:
(BOSSBS-1338R-CY7)
Fournisseur:
Bioss
Description:
Binding of anti-Fx1A to Heymann nephritis antigens (HA) on rat glomerular epithelial cells (GECs) in culture leads to capping and disappearance of antigens from the cell surface. This process may contribute to the formation of glomerular subepithelial immune deposits in vivo. The authors differentially extracted GECs to determine whether HA redistribution is mediated by cytoskeletal components. Observations were made by phase-contrast and immunofluorescence microscopy on primary and passaged GECs in monolayer culture and by spectrofluorimetry on GECs in suspension.
UOM:
1 * 100 µl
Fournisseur:
Lenz Laborglas GmbH & CO.KG
Description:
DURAN®, Borosilicate glass.
Numéro de catalogue:
(BOSSBS-1338R-A488)
Fournisseur:
Bioss
Description:
Binding of anti-Fx1A to Heymann nephritis antigens (HA) on rat glomerular epithelial cells (GECs) in culture leads to capping and disappearance of antigens from the cell surface. This process may contribute to the formation of glomerular subepithelial immune deposits in vivo. The authors differentially extracted GECs to determine whether HA redistribution is mediated by cytoskeletal components. Observations were made by phase-contrast and immunofluorescence microscopy on primary and passaged GECs in monolayer culture and by spectrofluorimetry on GECs in suspension.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1338R-A350)
Fournisseur:
Bioss
Description:
Binding of anti-Fx1A to Heymann nephritis antigens (HA) on rat glomerular epithelial cells (GECs) in culture leads to capping and disappearance of antigens from the cell surface. This process may contribute to the formation of glomerular subepithelial immune deposits in vivo. The authors differentially extracted GECs to determine whether HA redistribution is mediated by cytoskeletal components. Observations were made by phase-contrast and immunofluorescence microscopy on primary and passaged GECs in monolayer culture and by spectrofluorimetry on GECs in suspension.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1338R-A647)
Fournisseur:
Bioss
Description:
Binding of anti-Fx1A to Heymann nephritis antigens (HA) on rat glomerular epithelial cells (GECs) in culture leads to capping and disappearance of antigens from the cell surface. This process may contribute to the formation of glomerular subepithelial immune deposits in vivo. The authors differentially extracted GECs to determine whether HA redistribution is mediated by cytoskeletal components. Observations were made by phase-contrast and immunofluorescence microscopy on primary and passaged GECs in monolayer culture and by spectrofluorimetry on GECs in suspension.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13096R-CY7)
Fournisseur:
Bioss
Description:
ABT1 (activator of basal transcription 1) is a nuclear protein that associates with the TATA-binding protein (TBP) and enhances basal transcription activity of class II promoters. ABT1 associates with TBP in HeLa nuclear extracts in vitro. Another protein, designated ERF, is a member of the Ets family of transcription factors. The members of the Ets family are grouped because they share a highly conserved DNA binding domain. These factors are involved in growth factor pathways and regulate both proliferation and differentiation. ERF (Ets-2 repressor factor) is a ubiquitously expressed Ets-domain protein that exhibits strong transcriptional repressor activity, suppresses Ets-induced transformation and is regulated by MAPK phosphorylation. ERF transcription may be regulated by Ets-domain proteins. Additionally, modulation of ERF activity is involved in the transcriptional regulation of genes activated during entry into G1 phase.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1338R-A555)
Fournisseur:
Bioss
Description:
Binding of anti-Fx1A to Heymann nephritis antigens (HA) on rat glomerular epithelial cells (GECs) in culture leads to capping and disappearance of antigens from the cell surface. This process may contribute to the formation of glomerular subepithelial immune deposits in vivo. The authors differentially extracted GECs to determine whether HA redistribution is mediated by cytoskeletal components. Observations were made by phase-contrast and immunofluorescence microscopy on primary and passaged GECs in monolayer culture and by spectrofluorimetry on GECs in suspension.
UOM:
1 * 100 µl
Fournisseur:
Merck
Description:
La sélectivité de la colonne ZIC®-HILIC est idéale pour une vaste gamme de molécules contenant des groupes fonctionnels hydrophiles ou ionisables. Cela inclut les composés tels que les hydrates de carbone, les métabolites, les acides et les bases, les ions organiques et inorganiques, les complexes métalliques, les acides aminés, les peptides, les protéines dégradées, les extraits de plantes et de cellules, etc. Ces composés sont généralement caractérisés par une valeur LogP faible ou négative et ont une faible rétention sur les colonnes en phase inverse.
Numéro de catalogue:
(BOSSBS-13096R-CY3)
Fournisseur:
Bioss
Description:
ABT1 (activator of basal transcription 1) is a nuclear protein that associates with the TATA-binding protein (TBP) and enhances basal transcription activity of class II promoters. ABT1 associates with TBP in HeLa nuclear extracts in vitro. Another protein, designated ERF, is a member of the Ets family of transcription factors. The members of the Ets family are grouped because they share a highly conserved DNA binding domain. These factors are involved in growth factor pathways and regulate both proliferation and differentiation. ERF (Ets-2 repressor factor) is a ubiquitously expressed Ets-domain protein that exhibits strong transcriptional repressor activity, suppresses Ets-induced transformation and is regulated by MAPK phosphorylation. ERF transcription may be regulated by Ets-domain proteins. Additionally, modulation of ERF activity is involved in the transcriptional regulation of genes activated during entry into G1 phase.
UOM:
1 * 100 µl
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