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Pfizer Inc development termination
Development Termination, supplied by Pfizer Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/development termination/product/Pfizer Inc
Average 86 stars, based on 1 article reviews
development termination - by Bioz Stars, 2026-05
86/100 stars

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Pfizer Inc development termination
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Santa Cruz Biotechnology donkey polyclonal antibody developed against c-terminal calnexin peptide
a, comparison of MUGS activity (nanomoles/mg of total cell protein/h) in the postnuclear supernatant (PNS) and lysosome-enriched (Lyso.) fraction from untreated (open bar) and NGT (0.9 mM) treated (filled bar) ATSD fibroblasts. b, Western blots comparing the levels of α-subunits of Hex (α Hex), mature β-subunits of Hex (β Hex), glucocerebrosidase (Gcase), and <t>calnexin</t> in the PNS and lysosomal fractions (Lyso.) from untreated and NGT-treated ATSD cells. Position of relevant Mr markers (in kDa) are shown to the left of the blots. One microgram of total protein from each of the PNS and lysosomal fractions were analyzed.
Donkey Polyclonal Antibody Developed Against C Terminal Calnexin Peptide, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Millipore polyclonal antibody developed rabbit c-terminal actin fragment
a, comparison of MUGS activity (nanomoles/mg of total cell protein/h) in the postnuclear supernatant (PNS) and lysosome-enriched (Lyso.) fraction from untreated (open bar) and NGT (0.9 mM) treated (filled bar) ATSD fibroblasts. b, Western blots comparing the levels of α-subunits of Hex (α Hex), mature β-subunits of Hex (β Hex), glucocerebrosidase (Gcase), and <t>calnexin</t> in the PNS and lysosomal fractions (Lyso.) from untreated and NGT-treated ATSD cells. Position of relevant Mr markers (in kDa) are shown to the left of the blots. One microgram of total protein from each of the PNS and lysosomal fractions were analyzed.
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Vollrath post-developing rat photoreceptor terminals
a, comparison of MUGS activity (nanomoles/mg of total cell protein/h) in the postnuclear supernatant (PNS) and lysosome-enriched (Lyso.) fraction from untreated (open bar) and NGT (0.9 mM) treated (filled bar) ATSD fibroblasts. b, Western blots comparing the levels of α-subunits of Hex (α Hex), mature β-subunits of Hex (β Hex), glucocerebrosidase (Gcase), and <t>calnexin</t> in the PNS and lysosomal fractions (Lyso.) from untreated and NGT-treated ATSD cells. Position of relevant Mr markers (in kDa) are shown to the left of the blots. One microgram of total protein from each of the PNS and lysosomal fractions were analyzed.
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a, comparison of MUGS activity (nanomoles/mg of total cell protein/h) in the postnuclear supernatant (PNS) and lysosome-enriched (Lyso.) fraction from untreated (open bar) and NGT (0.9 mM) treated (filled bar) ATSD fibroblasts. b, Western blots comparing the levels of α-subunits of Hex (α Hex), mature β-subunits of Hex (β Hex), glucocerebrosidase (Gcase), and calnexin in the PNS and lysosomal fractions (Lyso.) from untreated and NGT-treated ATSD cells. Position of relevant Mr markers (in kDa) are shown to the left of the blots. One microgram of total protein from each of the PNS and lysosomal fractions were analyzed.

Journal:

Article Title: Pharmacological Enhancement of β -Hexosaminidase Activity in Fibroblasts from Adult Tay-Sachs and Sandhoff Patients *

doi: 10.1074/jbc.M308523200

Figure Lengend Snippet: a, comparison of MUGS activity (nanomoles/mg of total cell protein/h) in the postnuclear supernatant (PNS) and lysosome-enriched (Lyso.) fraction from untreated (open bar) and NGT (0.9 mM) treated (filled bar) ATSD fibroblasts. b, Western blots comparing the levels of α-subunits of Hex (α Hex), mature β-subunits of Hex (β Hex), glucocerebrosidase (Gcase), and calnexin in the PNS and lysosomal fractions (Lyso.) from untreated and NGT-treated ATSD cells. Position of relevant Mr markers (in kDa) are shown to the left of the blots. One microgram of total protein from each of the PNS and lysosomal fractions were analyzed.

Article Snippet: Donkey polyclonal antibody developed against a C-terminal calnexin peptide was purchased from Santa Cruz Biotechnology.

Techniques: Activity Assay, Western Blot