mouse multiple-tissue northern blot (TaKaRa)
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mouse multiple-tissue northern blot
Mouse Multiple Tissue Northern Blot, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+multiple-tissue+northern+blot/Mouse+MTC+Panel+III/pmc04681538-157-10-14
Average 95 stars, based on 10 article reviews
Mouse Multiple Tissue Northern Blot, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+multiple-tissue+northern+blot/Mouse+MTC+Panel+III/pmc04681538-157-10-14
Average 95 stars, based on 10 article reviews
mouse multiple-tissue northern blot - by Bioz Stars,
2026-09
95/100 stars
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Expressing:Article Title: Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: interaction of its intracellular domain with Myt1l. Article Snippet: Lingo-1 (also known as Lern1) is a component of the Nogo receptor complex that mediates intracellular signaling in response to myelin associated inhibitors (MAIs): NogoA, MAG, and Omgp.. Signaling through Nogo receptor extends to more than its well known role in preventing axon regeneration after lesion in the CNS, being implicated in neuronal functional maturation.. Using Lingo-1-deficient mice, it has been demonstrated that Lingo-1 plays relevant roles in oligodendrocyte differentiation during brain development, and that treatment with Lingo-1 antagonists can improve axon regeneration after lesion in adult mice by decreasing MAI mediated signaling. Article Title: Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage. Article Snippet: Recently, we identified a susceptibility locus for human uric acid nephrolithiasis (UAN) on 10q21–q22 and demonstrated that a novel gene (ZNF365) included in this region produces through alternative splicing several transcripts coding for four protein isoforms.. Mutation analysis showed that one of them (Talanin) is associated with UAN.. We examined the evolutionary conservation of ZNF365 gene through a comparative genomic approach. Article Title: Mice Deficient in Glutathione Transferase Zeta/Maleylacetoacetate Isomerase Exhibit a Range of Pathological Changes and Elevated Expression of Alpha, Mu, and Pi Class Glutathione Transferases Article Snippet: Northern Blotting Analysis A Article Title: Hereditary Spastic Paraplegia-Linked REEP1 Modulates ER-Mitochondria Contacts Article Snippet: Adult tissue Northern blotting was performed as previously described using Article Title: Characterization of the murine gene corresponding to human Hermansky-Pudlak syndrome type 3: exclusion of the Subtle gray (sut) locus. Article Snippet: Hermansky-Pudlak syndrome (HPS) consists of oculocutaneous albinism and a bleeding diathesis due to absent platelet dense bodies.. In addition to exhibiting considerable phenotypic variation, this autosomal recessive disorder displays locus heterogeneity.. One causative gene is HPS1, codng for a protein of unknown function and resultng in HPS-1 disease, common in northwest uerto Rico. Article Title: claudin-18 , a Novel Downstream Target Gene for the T/EBP/NKX2.1 Homeodomain Transcription Factor, Encodes Lung- and Stomach-Specific Isoforms through Alternative Splicing Article Snippet: A Article Title: Slc25a13 -Knockout Mice Harbor Metabolic Deficits but Fail To Display Hallmarks of Adult-Onset Type II Citrullinemia Article Snippet: Wild-type mRNA expression was determined by using a Article Title: Reduction of all-trans-retinal in the mouse liver peroxisome fraction by the short-chain dehydrogenase/reductase RRD: induction by the PPAR alpha ligand clofibrate. Article Snippet: The mouse liver 16000g fraction, which contains peroxisomes, reduces all-trans-retinal, but has limited ability to dehydrogenate retinol enzymatically.. Feeding mice for 2 weeks with a diet containing clofibrate (0.5%, w/w), a PPARR ligand and peroxisome proliferator, increased the 16000g fraction ∼2fold in protein, ∼2-fold in specific activity of retinal reduction, and ∼4-fold in retinal reductase units compared to controls, and caused a 50% decrease in liver retinol.. An increase in both reductase specific activity and units indicates that clofibrate/PPARR induced expression of retinal-reducing enzymes(s), in addition to increasing reductase(s) content. Northern Blot:Article Title: Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: interaction of its intracellular domain with Myt1l. Article Snippet: Lingo-1 (also known as Lern1) is a component of the Nogo receptor complex that mediates intracellular signaling in response to myelin associated inhibitors (MAIs): NogoA, MAG, and Omgp.. Signaling through Nogo receptor extends to more than its well known role in preventing axon regeneration after lesion in the CNS, being implicated in neuronal functional maturation.. Using Lingo-1-deficient mice, it has been demonstrated that Lingo-1 plays relevant roles in oligodendrocyte differentiation during brain development, and that treatment with Lingo-1 antagonists can improve axon regeneration after lesion in adult mice by decreasing MAI mediated signaling. Article Title: Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage. Article Snippet: Recently, we identified a susceptibility locus for human uric acid nephrolithiasis (UAN) on 10q21–q22 and demonstrated that a novel gene (ZNF365) included in this region produces through alternative splicing several transcripts coding for four protein isoforms.. Mutation analysis showed that one of them (Talanin) is associated with UAN.. We examined the evolutionary conservation of ZNF365 gene through a comparative genomic approach. Article Title: Mice Deficient in Glutathione Transferase Zeta/Maleylacetoacetate Isomerase Exhibit a Range of Pathological Changes and Elevated Expression of Alpha, Mu, and Pi Class Glutathione Transferases Article Snippet: Northern Blotting Analysis A Article Title: Hereditary Spastic Paraplegia-Linked REEP1 Modulates ER-Mitochondria Contacts Article Snippet: Adult tissue Northern blotting was performed as previously described using Article Title: Characterization of the murine gene corresponding to human Hermansky-Pudlak syndrome type 3: exclusion of the Subtle gray (sut) locus. Article Snippet: Hermansky-Pudlak syndrome (HPS) consists of oculocutaneous albinism and a bleeding diathesis due to absent platelet dense bodies.. In addition to exhibiting considerable phenotypic variation, this autosomal recessive disorder displays locus heterogeneity.. One causative gene is HPS1, codng for a protein of unknown function and resultng in HPS-1 disease, common in northwest uerto Rico. Article Title: claudin-18 , a Novel Downstream Target Gene for the T/EBP/NKX2.1 Homeodomain Transcription Factor, Encodes Lung- and Stomach-Specific Isoforms through Alternative Splicing Article Snippet: A Article Title: Slc25a13 -Knockout Mice Harbor Metabolic Deficits but Fail To Display Hallmarks of Adult-Onset Type II Citrullinemia Article Snippet: Wild-type mRNA expression was determined by using a Article Title: Reduction of all-trans-retinal in the mouse liver peroxisome fraction by the short-chain dehydrogenase/reductase RRD: induction by the PPAR alpha ligand clofibrate. Article Snippet: The mouse liver 16000g fraction, which contains peroxisomes, reduces all-trans-retinal, but has limited ability to dehydrogenate retinol enzymatically.. Feeding mice for 2 weeks with a diet containing clofibrate (0.5%, w/w), a PPARR ligand and peroxisome proliferator, increased the 16000g fraction ∼2fold in protein, ∼2-fold in specific activity of retinal reduction, and ∼4-fold in retinal reductase units compared to controls, and caused a 50% decrease in liver retinol.. An increase in both reductase specific activity and units indicates that clofibrate/PPARR induced expression of retinal-reducing enzymes(s), in addition to increasing reductase(s) content. Dot Blot:Article Title: Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: interaction of its intracellular domain with Myt1l. Article Snippet: Lingo-1 (also known as Lern1) is a component of the Nogo receptor complex that mediates intracellular signaling in response to myelin associated inhibitors (MAIs): NogoA, MAG, and Omgp.. Signaling through Nogo receptor extends to more than its well known role in preventing axon regeneration after lesion in the CNS, being implicated in neuronal functional maturation.. Using Lingo-1-deficient mice, it has been demonstrated that Lingo-1 plays relevant roles in oligodendrocyte differentiation during brain development, and that treatment with Lingo-1 antagonists can improve axon regeneration after lesion in adult mice by decreasing MAI mediated signaling. Article Title: Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage. Article Snippet: Recently, we identified a susceptibility locus for human uric acid nephrolithiasis (UAN) on 10q21–q22 and demonstrated that a novel gene (ZNF365) included in this region produces through alternative splicing several transcripts coding for four protein isoforms.. Mutation analysis showed that one of them (Talanin) is associated with UAN.. We examined the evolutionary conservation of ZNF365 gene through a comparative genomic approach. Article Title: Mice Deficient in Glutathione Transferase Zeta/Maleylacetoacetate Isomerase Exhibit a Range of Pathological Changes and Elevated Expression of Alpha, Mu, and Pi Class Glutathione Transferases Article Snippet: Northern Blotting Analysis A Article Title: Hereditary Spastic Paraplegia-Linked REEP1 Modulates ER-Mitochondria Contacts Article Snippet: Adult tissue Northern blotting was performed as previously described using Article Title: Characterization of the murine gene corresponding to human Hermansky-Pudlak syndrome type 3: exclusion of the Subtle gray (sut) locus. Article Snippet: Hermansky-Pudlak syndrome (HPS) consists of oculocutaneous albinism and a bleeding diathesis due to absent platelet dense bodies.. In addition to exhibiting considerable phenotypic variation, this autosomal recessive disorder displays locus heterogeneity.. One causative gene is HPS1, codng for a protein of unknown function and resultng in HPS-1 disease, common in northwest uerto Rico. Article Title: claudin-18 , a Novel Downstream Target Gene for the T/EBP/NKX2.1 Homeodomain Transcription Factor, Encodes Lung- and Stomach-Specific Isoforms through Alternative Splicing Article Snippet: A Article Title: Slc25a13 -Knockout Mice Harbor Metabolic Deficits but Fail To Display Hallmarks of Adult-Onset Type II Citrullinemia Article Snippet: Wild-type mRNA expression was determined by using a Article Title: Reduction of all-trans-retinal in the mouse liver peroxisome fraction by the short-chain dehydrogenase/reductase RRD: induction by the PPAR alpha ligand clofibrate. Article Snippet: The mouse liver 16000g fraction, which contains peroxisomes, reduces all-trans-retinal, but has limited ability to dehydrogenate retinol enzymatically.. Feeding mice for 2 weeks with a diet containing clofibrate (0.5%, w/w), a PPARR ligand and peroxisome proliferator, increased the 16000g fraction ∼2fold in protein, ∼2-fold in specific activity of retinal reduction, and ∼4-fold in retinal reductase units compared to controls, and caused a 50% decrease in liver retinol.. An increase in both reductase specific activity and units indicates that clofibrate/PPARR induced expression of retinal-reducing enzymes(s), in addition to increasing reductase(s) content. Mutagenesis:Article Title: Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: interaction of its intracellular domain with Myt1l. Article Snippet: Lingo-1 (also known as Lern1) is a component of the Nogo receptor complex that mediates intracellular signaling in response to myelin associated inhibitors (MAIs): NogoA, MAG, and Omgp.. Signaling through Nogo receptor extends to more than its well known role in preventing axon regeneration after lesion in the CNS, being implicated in neuronal functional maturation.. Using Lingo-1-deficient mice, it has been demonstrated that Lingo-1 plays relevant roles in oligodendrocyte differentiation during brain development, and that treatment with Lingo-1 antagonists can improve axon regeneration after lesion in adult mice by decreasing MAI mediated signaling. Article Title: Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage. Article Snippet: Recently, we identified a susceptibility locus for human uric acid nephrolithiasis (UAN) on 10q21–q22 and demonstrated that a novel gene (ZNF365) included in this region produces through alternative splicing several transcripts coding for four protein isoforms.. Mutation analysis showed that one of them (Talanin) is associated with UAN.. We examined the evolutionary conservation of ZNF365 gene through a comparative genomic approach. Article Title: Mice Deficient in Glutathione Transferase Zeta/Maleylacetoacetate Isomerase Exhibit a Range of Pathological Changes and Elevated Expression of Alpha, Mu, and Pi Class Glutathione Transferases Article Snippet: Northern Blotting Analysis A Article Title: Hereditary Spastic Paraplegia-Linked REEP1 Modulates ER-Mitochondria Contacts Article Snippet: Adult tissue Northern blotting was performed as previously described using Article Title: Characterization of the murine gene corresponding to human Hermansky-Pudlak syndrome type 3: exclusion of the Subtle gray (sut) locus. Article Snippet: Hermansky-Pudlak syndrome (HPS) consists of oculocutaneous albinism and a bleeding diathesis due to absent platelet dense bodies.. In addition to exhibiting considerable phenotypic variation, this autosomal recessive disorder displays locus heterogeneity.. One causative gene is HPS1, codng for a protein of unknown function and resultng in HPS-1 disease, common in northwest uerto Rico. Article Title: claudin-18 , a Novel Downstream Target Gene for the T/EBP/NKX2.1 Homeodomain Transcription Factor, Encodes Lung- and Stomach-Specific Isoforms through Alternative Splicing Article Snippet: A Article Title: Slc25a13 -Knockout Mice Harbor Metabolic Deficits but Fail To Display Hallmarks of Adult-Onset Type II Citrullinemia Article Snippet: Wild-type mRNA expression was determined by using a Article Title: Reduction of all-trans-retinal in the mouse liver peroxisome fraction by the short-chain dehydrogenase/reductase RRD: induction by the PPAR alpha ligand clofibrate. Article Snippet: The mouse liver 16000g fraction, which contains peroxisomes, reduces all-trans-retinal, but has limited ability to dehydrogenate retinol enzymatically.. Feeding mice for 2 weeks with a diet containing clofibrate (0.5%, w/w), a PPARR ligand and peroxisome proliferator, increased the 16000g fraction ∼2fold in protein, ∼2-fold in specific activity of retinal reduction, and ∼4-fold in retinal reductase units compared to controls, and caused a 50% decrease in liver retinol.. An increase in both reductase specific activity and units indicates that clofibrate/PPARR induced expression of retinal-reducing enzymes(s), in addition to increasing reductase(s) content. Reverse Transcription Polymerase Chain Reaction:Article Title: Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: interaction of its intracellular domain with Myt1l. Article Snippet: Lingo-1 (also known as Lern1) is a component of the Nogo receptor complex that mediates intracellular signaling in response to myelin associated inhibitors (MAIs): NogoA, MAG, and Omgp.. Signaling through Nogo receptor extends to more than its well known role in preventing axon regeneration after lesion in the CNS, being implicated in neuronal functional maturation.. Using Lingo-1-deficient mice, it has been demonstrated that Lingo-1 plays relevant roles in oligodendrocyte differentiation during brain development, and that treatment with Lingo-1 antagonists can improve axon regeneration after lesion in adult mice by decreasing MAI mediated signaling. Article Title: Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage. Article Snippet: Recently, we identified a susceptibility locus for human uric acid nephrolithiasis (UAN) on 10q21–q22 and demonstrated that a novel gene (ZNF365) included in this region produces through alternative splicing several transcripts coding for four protein isoforms.. Mutation analysis showed that one of them (Talanin) is associated with UAN.. We examined the evolutionary conservation of ZNF365 gene through a comparative genomic approach. Article Title: Mice Deficient in Glutathione Transferase Zeta/Maleylacetoacetate Isomerase Exhibit a Range of Pathological Changes and Elevated Expression of Alpha, Mu, and Pi Class Glutathione Transferases Article Snippet: Northern Blotting Analysis A Article Title: Hereditary Spastic Paraplegia-Linked REEP1 Modulates ER-Mitochondria Contacts Article Snippet: Adult tissue Northern blotting was performed as previously described using Article Title: Characterization of the murine gene corresponding to human Hermansky-Pudlak syndrome type 3: exclusion of the Subtle gray (sut) locus. Article Snippet: Hermansky-Pudlak syndrome (HPS) consists of oculocutaneous albinism and a bleeding diathesis due to absent platelet dense bodies.. In addition to exhibiting considerable phenotypic variation, this autosomal recessive disorder displays locus heterogeneity.. One causative gene is HPS1, codng for a protein of unknown function and resultng in HPS-1 disease, common in northwest uerto Rico. Article Title: claudin-18 , a Novel Downstream Target Gene for the T/EBP/NKX2.1 Homeodomain Transcription Factor, Encodes Lung- and Stomach-Specific Isoforms through Alternative Splicing Article Snippet: A Article Title: Slc25a13 -Knockout Mice Harbor Metabolic Deficits but Fail To Display Hallmarks of Adult-Onset Type II Citrullinemia Article Snippet: Wild-type mRNA expression was determined by using a Article Title: Reduction of all-trans-retinal in the mouse liver peroxisome fraction by the short-chain dehydrogenase/reductase RRD: induction by the PPAR alpha ligand clofibrate. Article Snippet: The mouse liver 16000g fraction, which contains peroxisomes, reduces all-trans-retinal, but has limited ability to dehydrogenate retinol enzymatically.. Feeding mice for 2 weeks with a diet containing clofibrate (0.5%, w/w), a PPARR ligand and peroxisome proliferator, increased the 16000g fraction ∼2fold in protein, ∼2-fold in specific activity of retinal reduction, and ∼4-fold in retinal reductase units compared to controls, and caused a 50% decrease in liver retinol.. An increase in both reductase specific activity and units indicates that clofibrate/PPARR induced expression of retinal-reducing enzymes(s), in addition to increasing reductase(s) content. |
