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Bar Harbor BioTechnology global pattern recognition software
Global Pattern Recognition Software, supplied by Bar Harbor BioTechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/global+pattern+recognition+software/global+pattern+recognition+data+analysis+tool/pmc03536038-95-9-14
Average 90 stars, based on 1 article reviews
global pattern recognition software - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Control:

Article Title: Fermented Mistletoe Extract as a Multimodal Antitumoral Agent in Gliomas
Article Snippet: For expression analysis of 96 genes involved in tumor cell motility and angiogenesis, Human Angiogenesis 96-well StellARray qPCR array (Lonza, Basel, Switzerland) was prepared according to manufacturer's instruction using SYBR green master mix (Thermo Fisher Scientific, MA, USA) on an ABI 7500 system. .. Data were analyzed with Global Pattern Recognition Data Analysis Tool (Bar Harbor Biotechnology, Trenton, ME, USA) using the internal array control housekeeping gene expression for normalization. .. The REMBRANDT database contains microarray data for probes from the Affymetrix U133 Plus 2.0 GeneChip (National Cancer Institute 2005; REMBRANDT home page: http://rembrandt.nci.nih.gov/ (accessed February 6, 2012)).

Article Title: Myeloperoxidase Oxidized LDL Interferes with Endothelial Cell Motility through miR-22 and Heme Oxygenase 1 Induction: Possible Involvement in Reendothelialization of Vascular Injuries
Article Snippet: For expression analysis of 94 preselected genes involved in angiogenesis, Human Angiogenesis 96-well StellARray qPCR array (Lonza Ltd., Switzerland) was used according to manufacturer's instruction with ABsolute qPCR SYBR Green ROX Mix (Thermo Scientific) on an ABI Prism 7900HT sequence detection system (Applied Biosystems). .. Data were analyzed with Global Pattern Recognition Data Analysis Tool (Bar Harbor Biotechnology, Trenton, ME, USA) using the internal array control housekeeping gene expression for normalization. .. The microRNA:mRNA target predictions were downloaded from public websites TargetScan algorithm release 4.1 ( http://www.targetscan.org ) and miRanda algorithm ( http://www.microrna.org ).

Gene Expression:

Article Title: Fermented Mistletoe Extract as a Multimodal Antitumoral Agent in Gliomas
Article Snippet: For expression analysis of 96 genes involved in tumor cell motility and angiogenesis, Human Angiogenesis 96-well StellARray qPCR array (Lonza, Basel, Switzerland) was prepared according to manufacturer's instruction using SYBR green master mix (Thermo Fisher Scientific, MA, USA) on an ABI 7500 system. .. Data were analyzed with Global Pattern Recognition Data Analysis Tool (Bar Harbor Biotechnology, Trenton, ME, USA) using the internal array control housekeeping gene expression for normalization. .. The REMBRANDT database contains microarray data for probes from the Affymetrix U133 Plus 2.0 GeneChip (National Cancer Institute 2005; REMBRANDT home page: http://rembrandt.nci.nih.gov/ (accessed February 6, 2012)).

Article Title: Myeloperoxidase Oxidized LDL Interferes with Endothelial Cell Motility through miR-22 and Heme Oxygenase 1 Induction: Possible Involvement in Reendothelialization of Vascular Injuries
Article Snippet: For expression analysis of 94 preselected genes involved in angiogenesis, Human Angiogenesis 96-well StellARray qPCR array (Lonza Ltd., Switzerland) was used according to manufacturer's instruction with ABsolute qPCR SYBR Green ROX Mix (Thermo Scientific) on an ABI Prism 7900HT sequence detection system (Applied Biosystems). .. Data were analyzed with Global Pattern Recognition Data Analysis Tool (Bar Harbor Biotechnology, Trenton, ME, USA) using the internal array control housekeeping gene expression for normalization. .. The microRNA:mRNA target predictions were downloaded from public websites TargetScan algorithm release 4.1 ( http://www.targetscan.org ) and miRanda algorithm ( http://www.microrna.org ).

other:

Article Title: Binge Ethanol Drinking Produces Sexually Divergent and Distinct Changes in Nucleus Accumbens Signaling Cascades and Pathways in Adult C57BL/6J Mice
Article Snippet: For the qPCR array data, Bar Harbor BioTechnology identified significantly changed genes in the data set using their Global Pattern Recognition (GPR) algorithm ( ).

Article Title: Molecular Mechanisms Underlying Delayed Apoptosis in Neutrophils from Multiple Trauma Patients with and without Sepsis
Article Snippet: Data were analyzed using Global Pattern Recognition (GPR) Analysis software (Bar Harbor Biotechnology), which normalizes the data of each analyzed gene to that of every other gene without dependence of single gene normalization ( 31 ).

Article Title: Coagulation Gene Expression Profiling in Infants With Necrotizing Enterocolitis
Article Snippet: Objectives: Coagulopathy and mesenteric thrombosis are common in premature neonates with necrotizing enterocolitis (NEC).. This pilot study aimed to investigate the hypothesis that there are changes in the gene expression related to the coagulation and anticoagulation systems in NEC.. Methods: Consecutive neonates (n=11) with NEC (Bell’s stages 2-3) were recruited.

Article Title: Molecular signatures of mood stabilisers highlight the role of the transcription factor REST/NRSF
Article Snippet: Changes in gene expression were analysed on the Lonza Web site ( http://array.lonza.com/gpr ), using the Global Pattern RecognitionTM (GPR) analysis software designed by Bar Harbor Biotechnology ( https://www.bhbio.com/BHB/dw/home.html ).

Saline:

Article Title: Opioid analgesics stop the development of clostridial gas gangrene.
Article Snippet: All cumulative threshold (Ct) values were standardized using Calqpelx (Eppendorf ). .. Data sets (saline tissues, compared with either wild-type or buprenorphine-pretreated wild-type tissues) were analyzed on the Lonza Web site (available at: http://array.lonza.com/gpr), using Global Pattern Recognition analysis software designed by Bar Harbor Biotechnology (available at: https://www.bhbio.com/BHB/dw/home.html), as previously described [27, 28], and as recommended by the manufacturer. ..

Software:

Article Title: Opioid analgesics stop the development of clostridial gas gangrene.
Article Snippet: All cumulative threshold (Ct) values were standardized using Calqpelx (Eppendorf ). .. Data sets (saline tissues, compared with either wild-type or buprenorphine-pretreated wild-type tissues) were analyzed on the Lonza Web site (available at: http://array.lonza.com/gpr), using Global Pattern Recognition analysis software designed by Bar Harbor Biotechnology (available at: https://www.bhbio.com/BHB/dw/home.html), as previously described [27, 28], and as recommended by the manufacturer. ..

Quantitative RT-PCR:

Article Title: Up-regulation of glutathione-related genes, enzyme activities and transport proteins in human cervical cancer cells treated with doxorubicin.
Article Snippet: Doxorubicin (DOX), one of the most effective anticancer drugs, acts in a variety of ways including DNA damage, enzyme inhibition and generation of reactive oxygen species.. Glutathione (GSH) and glutathione-related enzymes including: glutathione peroxidase (GPX), glutathione reductase (GSR) and glutathione S-transferases (GST) may play a role in adaptive detoxification processes in response to the oxidative stress, thus contributing to drug resistance phenotype.. In this study, we investigated effects of DOX treatment on expression and activity of GSH-related enzymes and multidrug resistanceassociated proteins in cultured human cervical cancer cells displaying different resistance against this drug (HeLa and KB-V1).



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( a – d ) CD11c dnR and wild type mice were injected ( i.p. ) twice a day with BrdU for 3 days. On day 3, mice were sacrificed and frequency of cycling cells was determined in the bone marrow. ( a – b ) FACS plots show the distribution of BrdU staining among total mNK cells ( a ) and gated mNK cells at stages D, E, and F ( b ). ( c ) Graph shows the frequency of cycling cells in pNK, iNK, and mNK cells from CD11c dnR (black circle) versus wild type (white circle) mice. ( d ) Graph shows the frequency of cycling cells in mNK cells at stages D, E, and F from CD11c dnR (black circle) versus wild type (white circle) mice. Data in a , d are representative of three independent experiments with n = 2 mice per experiment and results in c , d show all 6 individual mice. ( e – f ) mNK cells at stages D, E, and F were sorted from the bone marrow. mRNA was isolated and cDNA was subjected to pathway-specific qPCR for analysis of cell cycle genes ( e ) or SYBR Green qPCR for analysis of transcription factors T-bet, GATA-3, and IRF-2 ( f ). Data were analyzed using <t>Global</t> <t>Pattern</t> <t>Recognition</t> <t>analytical</t> <t>software</t> ( e ) or 2-33C3 method ( f ) and results were expressed as fold of change in CD11c dnR versus wild type samples. Data in e , f are representative of three independent cell sorting with samples pooled from n = 12 CD11c dnR and 25 WT mice.
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( a – d ) CD11c dnR and wild type mice were injected ( i.p. ) twice a day with BrdU for 3 days. On day 3, mice were sacrificed and frequency of cycling cells was determined in the bone marrow. ( a – b ) FACS plots show the distribution of BrdU staining among total mNK cells ( a ) and gated mNK cells at stages D, E, and F ( b ). ( c ) Graph shows the frequency of cycling cells in pNK, iNK, and mNK cells from CD11c dnR (black circle) versus wild type (white circle) mice. ( d ) Graph shows the frequency of cycling cells in mNK cells at stages D, E, and F from CD11c dnR (black circle) versus wild type (white circle) mice. Data in a , d are representative of three independent experiments with n = 2 mice per experiment and results in c , d show all 6 individual mice. ( e – f ) mNK cells at stages D, E, and F were sorted from the bone marrow. mRNA was isolated and cDNA was subjected to pathway-specific qPCR for analysis of cell cycle genes ( e ) or SYBR Green qPCR for analysis of transcription factors T-bet, GATA-3, and IRF-2 ( f ). Data were analyzed using <t>Global</t> <t>Pattern</t> <t>Recognition</t> <t>analytical</t> <t>software</t> ( e ) or 2-33C3 method ( f ) and results were expressed as fold of change in CD11c dnR versus wild type samples. Data in e , f are representative of three independent cell sorting with samples pooled from n = 12 CD11c dnR and 25 WT mice.
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( a – d ) CD11c dnR and wild type mice were injected ( i.p. ) twice a day with BrdU for 3 days. On day 3, mice were sacrificed and frequency of cycling cells was determined in the bone marrow. ( a – b ) FACS plots show the distribution of BrdU staining among total mNK cells ( a ) and gated mNK cells at stages D, E, and F ( b ). ( c ) Graph shows the frequency of cycling cells in pNK, iNK, and mNK cells from CD11c dnR (black circle) versus wild type (white circle) mice. ( d ) Graph shows the frequency of cycling cells in mNK cells at stages D, E, and F from CD11c dnR (black circle) versus wild type (white circle) mice. Data in a , d are representative of three independent experiments with n = 2 mice per experiment and results in c , d show all 6 individual mice. ( e – f ) mNK cells at stages D, E, and F were sorted from the bone marrow. mRNA was isolated and cDNA was subjected to pathway-specific qPCR for analysis of cell cycle genes ( e ) or SYBR Green qPCR for analysis of transcription factors T-bet, GATA-3, and IRF-2 ( f ). Data were analyzed using <t>Global</t> <t>Pattern</t> <t>Recognition</t> <t>analytical</t> <t>software</t> ( e ) or 2-33C3 method ( f ) and results were expressed as fold of change in CD11c dnR versus wild type samples. Data in e , f are representative of three independent cell sorting with samples pooled from n = 12 CD11c dnR and 25 WT mice.
Global Pattern Recognition Software, supplied by Bar Harbor BioTechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/global+pattern+recognition+software/global+pattern+recognition+data+analysis+tool/pmc03536038-95-9-14
Average 90 stars, based on 1 article reviews
global pattern recognition software - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

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( a – d ) CD11c dnR and wild type mice were injected ( i.p. ) twice a day with BrdU for 3 days. On day 3, mice were sacrificed and frequency of cycling cells was determined in the bone marrow. ( a – b ) FACS plots show the distribution of BrdU staining among total mNK cells ( a ) and gated mNK cells at stages D, E, and F ( b ). ( c ) Graph shows the frequency of cycling cells in pNK, iNK, and mNK cells from CD11c dnR (black circle) versus wild type (white circle) mice. ( d ) Graph shows the frequency of cycling cells in mNK cells at stages D, E, and F from CD11c dnR (black circle) versus wild type (white circle) mice. Data in a , d are representative of three independent experiments with n = 2 mice per experiment and results in c , d show all 6 individual mice. ( e – f ) mNK cells at stages D, E, and F were sorted from the bone marrow. mRNA was isolated and cDNA was subjected to pathway-specific qPCR for analysis of cell cycle genes ( e ) or SYBR Green qPCR for analysis of transcription factors T-bet, GATA-3, and IRF-2 ( f ). Data were analyzed using Global Pattern Recognition analytical software ( e ) or 2-33C3 method ( f ) and results were expressed as fold of change in CD11c dnR versus wild type samples. Data in e , f are representative of three independent cell sorting with samples pooled from n = 12 CD11c dnR and 25 WT mice.

Journal: Nature immunology

Article Title: TGF-β is responsible for NK cell immaturity during ontogeny and increased susceptibility to infection during mouse infancy

doi: 10.1038/ni.2388

Figure Lengend Snippet: ( a – d ) CD11c dnR and wild type mice were injected ( i.p. ) twice a day with BrdU for 3 days. On day 3, mice were sacrificed and frequency of cycling cells was determined in the bone marrow. ( a – b ) FACS plots show the distribution of BrdU staining among total mNK cells ( a ) and gated mNK cells at stages D, E, and F ( b ). ( c ) Graph shows the frequency of cycling cells in pNK, iNK, and mNK cells from CD11c dnR (black circle) versus wild type (white circle) mice. ( d ) Graph shows the frequency of cycling cells in mNK cells at stages D, E, and F from CD11c dnR (black circle) versus wild type (white circle) mice. Data in a , d are representative of three independent experiments with n = 2 mice per experiment and results in c , d show all 6 individual mice. ( e – f ) mNK cells at stages D, E, and F were sorted from the bone marrow. mRNA was isolated and cDNA was subjected to pathway-specific qPCR for analysis of cell cycle genes ( e ) or SYBR Green qPCR for analysis of transcription factors T-bet, GATA-3, and IRF-2 ( f ). Data were analyzed using Global Pattern Recognition analytical software ( e ) or 2-33C3 method ( f ) and results were expressed as fold of change in CD11c dnR versus wild type samples. Data in e , f are representative of three independent cell sorting with samples pooled from n = 12 CD11c dnR and 25 WT mice.

Article Snippet: For cell cycle genes, we used a customized cell cycle qPCR array according to the manufacturer’s instructions (Lonza), and data were analyzed using Global Pattern Recognition analytical software (Lonza).

Techniques: Injection, BrdU Staining, Isolation, SYBR Green Assay, Software, FACS