functions for the compression of a bivariate discrete measure Search Results


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Glaxo Smith ofa
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
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Konan Medical USA ofa
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
Ofa, supplied by Konan Medical USA, 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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Genmab Inc ofa
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
Ofa, supplied by Genmab Inc, 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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Emisphere ofa
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
Ofa, supplied by Emisphere, 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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Nacalai a. ureafaciens sialidase nacalai tesque
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
A. Ureafaciens Sialidase Nacalai Tesque, supplied by Nacalai, 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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Rieser GmbH ofa-ilrp
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
Ofa Ilrp, supplied by Rieser GmbH, 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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Dawley Inc sprague–dawley (ofa-sd) rat strain
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
Sprague–Dawley (Ofa Sd) Rat Strain, supplied by Dawley Inc, 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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Raytest GmbH minigita ofa probe
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
Minigita Ofa Probe, supplied by Raytest GmbH, 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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Raytest GmbH elysia-raytest minigita tlc reader with ofa probe and tungsten collimator
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
Elysia Raytest Minigita Tlc Reader With Ofa Probe And Tungsten Collimator, supplied by Raytest GmbH, 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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Thorlabs photodetector det01cfc/m
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
Photodetector Det01cfc/M, supplied by Thorlabs, 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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Rongcheng Mashan Group Co Ltd a. coerulea ephyrae
CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of <t>ofatumumab</t> <t>(OFA)</t> were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.
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CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of ofatumumab (OFA) were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.

Journal: Journal of immunology (Baltimore, Md. : 1950)

Article Title: Induced Resistance to Ofatumumab Mediated Cell Clearance Mechanisms, Including Complement Dependent Cytotoxicity, in Chronic Lymphocytic Leukemia

doi: 10.4049/jimmunol.1302954

Figure Lengend Snippet: CLL cells obtained from patients before treatment (0hr), and then at 8hr and 24hr after the start of the administration of the first dose of ofatumumab (OFA) were tested for in vitro CDC using saturating doses (10 μg/ml) of rituximab (RTX), OFA, or alemtuzumab (ALM)and 10% normal human serum (NHS) as a source of complement. RTX induced low levels of CDC. Compared to OFA CDC in pre-treatment specimens (median 37% cytotoxicity, range 0 – 83) there was a significant decrease in OFA CDC at 8hr (median 0%, range 0 – 5)(p<0.0001) and 24hr (median 0%, range 0 – 32) (p<0.0001). In contrast, ALM CDC was not decreased by in vivo exposure of CLL cells to OFA.

Article Snippet: OFA standards were prepared by serial dilutions of a commercial sample of OFA (GlaxoSmithKline, Research Triangle Park, NC) into pooled normal human serum.

Techniques: In Vitro, In Vivo