code for arginine Search Results


96
Biosynth Carbosynth cyclic tripeptide arginine glycine aspartate
Cyclic Tripeptide Arginine Glycine Aspartate, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Millipore linolenic acid (lna) isomers cod 47792
Ingredients, <t> chemical </t> composition, and fatty acids profile of the experimental concentrates and of the hay and rolled barley administered to the ewes.
Linolenic Acid (Lna) Isomers Cod 47792, supplied by Millipore, 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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Qiagen lna u6 positive control probe
In situ hybridisation showing miR-206 localization in transversal section of vastus lateralis muscle from one DM1 patient and one control subject . 4a: Tissue distribution of miR-206 in an healthy subject. miR-206 was expressed mostly in nuclear regions. 4b: Tissue distribuition of miR-206 in a DM1 patient. The miR-206 strongest signal corresponds to nuclear clumps (red arrow). Expression of miR-206 was also observed in nuclear regions of centralized nuclei. 4c: hybridization of <t>U6-siRNA</t> <t>LNA</t> used as positive control. 4d: LNA probe with a scrambled sequence, which is not present in the human genome, has been used to test the specificity of the probes. Green signal corresponds to lipofuscin-derived autofluorescence of the muscle tissue and does not localize with the nuclei.
Lna U6 Positive Control Probe, supplied by Qiagen, 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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Colgate-Palmolive prorelief (cpr
In situ hybridisation showing miR-206 localization in transversal section of vastus lateralis muscle from one DM1 patient and one control subject . 4a: Tissue distribution of miR-206 in an healthy subject. miR-206 was expressed mostly in nuclear regions. 4b: Tissue distribuition of miR-206 in a DM1 patient. The miR-206 strongest signal corresponds to nuclear clumps (red arrow). Expression of miR-206 was also observed in nuclear regions of centralized nuclei. 4c: hybridization of <t>U6-siRNA</t> <t>LNA</t> used as positive control. 4d: LNA probe with a scrambled sequence, which is not present in the human genome, has been used to test the specificity of the probes. Green signal corresponds to lipofuscin-derived autofluorescence of the muscle tissue and does not localize with the nuclei.
Prorelief (Cpr, supplied by Colgate-Palmolive, 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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Average 90 stars, based on 1 article reviews
prorelief (cpr - by Bioz Stars, 2026-04
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Millipore nα-benzoyl-dl-arginine 4-nitroanilide hydrochloride (code b4875)
In situ hybridisation showing miR-206 localization in transversal section of vastus lateralis muscle from one DM1 patient and one control subject . 4a: Tissue distribution of miR-206 in an healthy subject. miR-206 was expressed mostly in nuclear regions. 4b: Tissue distribuition of miR-206 in a DM1 patient. The miR-206 strongest signal corresponds to nuclear clumps (red arrow). Expression of miR-206 was also observed in nuclear regions of centralized nuclei. 4c: hybridization of <t>U6-siRNA</t> <t>LNA</t> used as positive control. 4d: LNA probe with a scrambled sequence, which is not present in the human genome, has been used to test the specificity of the probes. Green signal corresponds to lipofuscin-derived autofluorescence of the muscle tissue and does not localize with the nuclei.
Nα Benzoyl Dl Arginine 4 Nitroanilide Hydrochloride (Code B4875), supplied by Millipore, 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 arg l-arginine hydrochloride salt
In situ hybridisation showing miR-206 localization in transversal section of vastus lateralis muscle from one DM1 patient and one control subject . 4a: Tissue distribution of miR-206 in an healthy subject. miR-206 was expressed mostly in nuclear regions. 4b: Tissue distribuition of miR-206 in a DM1 patient. The miR-206 strongest signal corresponds to nuclear clumps (red arrow). Expression of miR-206 was also observed in nuclear regions of centralized nuclei. 4c: hybridization of <t>U6-siRNA</t> <t>LNA</t> used as positive control. 4d: LNA probe with a scrambled sequence, which is not present in the human genome, has been used to test the specificity of the probes. Green signal corresponds to lipofuscin-derived autofluorescence of the muscle tissue and does not localize with the nuclei.
Arg L Arginine Hydrochloride Salt, supplied by Millipore, 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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Qiagen fluorescein-labelled lna oligonucleotides
<t>miR-17/20a</t> and Trp53inp1 role in NSC self-renewal. ( A ) Bright-field images of secondary neurosphere-forming assay of NSC transfected with <t>LNA-anti-miR-17/20a</t> alone or in combination with siTrp53inp1 (scale bar, 50 mm). ( B ) Histogram shows the percentage of neurosphere-forming cells after single or combined LNA anti-miR, their combination and the association with siTrp53inp1. Bars represent the mean of three independent experiments ±s.d. * P <0.05 versus siCtrl ** P <0.05 versus LNA miR-17/20a. ( C ) Secondary neurosphere-forming assay after silencing of Nanog alone (siNanog) or in combination with siTrp53inp1 or overexpression of miR-17/20a, compared with siCtrl. Graph error bars indicate s.d. calculated on at least three independent experiments. * P <0.05 versus LNA-siCtrl ** P <0.05 versus siNanog. ( D ) Model illustrating the coordinated loop among Nanog, p53 and Trp53inp1, centred on miR-17-92 cluster. In NSC, miR-17-92 cluster is regulated by Nanog that is in turn controlled by Hh signalling and p53 . Additional activities of p53 are the direct repression of miR-17/92 cluster and Hh/Gli . In turn, miR-17 and miR-20a, members of miR-17-92 cluster, target and inhibit Trp53inp1 (this study) that inhibits stem cell self-renewal. Red double-arrow line shows the induction of Trp53inp1 by p53 and the backward positive regulation of p53 by Trp53inp1. For further details, see text and references herein.
Fluorescein Labelled Lna Oligonucleotides, supplied by Qiagen, 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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Qiagen mircury lna mirna pcr assay
Correlation coefficients between <t> miRNA </t> expression and independent variables in the WEA cohort according to Spearman.
Mircury Lna Mirna Pcr Assay, supplied by Qiagen, 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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Gene Codes Inc arg-gingipain
Correlation coefficients between <t> miRNA </t> expression and independent variables in the WEA cohort according to Spearman.
Arg Gingipain, supplied by Gene Codes 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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Thermo Fisher isotope-labeling dmem media (with 13 c6 l-lysine and 13 c6, 15 n4 l-arginine)
Correlation coefficients between <t> miRNA </t> expression and independent variables in the WEA cohort according to Spearman.
Isotope Labeling Dmem Media (With 13 C6 L Lysine And 13 C6, 15 N4 L Arginine), supplied by Thermo Fisher, 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/result/isotope-labeling dmem media (with 13 c6 l-lysine and 13 c6, 15 n4 l-arginine)/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
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Peptide Institute 4-methyl-7-coumarylamide (mca) peptide substrates, z-phe-arg-mca
Correlation coefficients between <t> miRNA </t> expression and independent variables in the WEA cohort according to Spearman.
4 Methyl 7 Coumarylamide (Mca) Peptide Substrates, Z Phe Arg Mca, supplied by Peptide Institute, 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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Average 90 stars, based on 1 article reviews
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Cambridge Isotope Laboratories l-arginine-hcl
Correlation coefficients between <t> miRNA </t> expression and independent variables in the WEA cohort according to Spearman.
L Arginine Hcl, supplied by Cambridge Isotope Laboratories, 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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Image Search Results


Ingredients,  chemical  composition, and fatty acids profile of the experimental concentrates and of the hay and rolled barley administered to the ewes.

Journal: BioMed Research International

Article Title: Effect of Dietary Chestnut or Quebracho Tannin Supplementation on Microbial Community and Fatty Acid Profile in the Rumen of Dairy Ewes

doi: 10.1155/2017/4969076

Figure Lengend Snippet: Ingredients, chemical composition, and fatty acids profile of the experimental concentrates and of the hay and rolled barley administered to the ewes.

Article Snippet: Moreover, standard mix of linolenic acid (LNA) isomers (cod 47792, Supelco, Chemical Co., St. Louis, MO, USA) and of LA isomers (cod 47791, Supelco, Chemical Co., St. Louis, MO, USA) and published isomeric profiles [ ] were used to identify the isomers of interest (conjugated α -linolenic acid, CALNA, 18:3 cis 9, trans 11, cis 15; vaccelenic acid, VLA, 18:2 trans 11, cis 15).

Techniques: Control

In situ hybridisation showing miR-206 localization in transversal section of vastus lateralis muscle from one DM1 patient and one control subject . 4a: Tissue distribution of miR-206 in an healthy subject. miR-206 was expressed mostly in nuclear regions. 4b: Tissue distribuition of miR-206 in a DM1 patient. The miR-206 strongest signal corresponds to nuclear clumps (red arrow). Expression of miR-206 was also observed in nuclear regions of centralized nuclei. 4c: hybridization of U6-siRNA LNA used as positive control. 4d: LNA probe with a scrambled sequence, which is not present in the human genome, has been used to test the specificity of the probes. Green signal corresponds to lipofuscin-derived autofluorescence of the muscle tissue and does not localize with the nuclei.

Journal: Journal of Translational Medicine

Article Title: Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients

doi: 10.1186/1479-5876-8-48

Figure Lengend Snippet: In situ hybridisation showing miR-206 localization in transversal section of vastus lateralis muscle from one DM1 patient and one control subject . 4a: Tissue distribution of miR-206 in an healthy subject. miR-206 was expressed mostly in nuclear regions. 4b: Tissue distribuition of miR-206 in a DM1 patient. The miR-206 strongest signal corresponds to nuclear clumps (red arrow). Expression of miR-206 was also observed in nuclear regions of centralized nuclei. 4c: hybridization of U6-siRNA LNA used as positive control. 4d: LNA probe with a scrambled sequence, which is not present in the human genome, has been used to test the specificity of the probes. Green signal corresponds to lipofuscin-derived autofluorescence of the muscle tissue and does not localize with the nuclei.

Article Snippet: EX100008999901), a LNA U6 positive control probe (Exiqon Cod.

Techniques: In Situ, Hybridization, Expressing, Positive Control, Sequencing, Derivative Assay

miR-17/20a and Trp53inp1 role in NSC self-renewal. ( A ) Bright-field images of secondary neurosphere-forming assay of NSC transfected with LNA-anti-miR-17/20a alone or in combination with siTrp53inp1 (scale bar, 50 mm). ( B ) Histogram shows the percentage of neurosphere-forming cells after single or combined LNA anti-miR, their combination and the association with siTrp53inp1. Bars represent the mean of three independent experiments ±s.d. * P <0.05 versus siCtrl ** P <0.05 versus LNA miR-17/20a. ( C ) Secondary neurosphere-forming assay after silencing of Nanog alone (siNanog) or in combination with siTrp53inp1 or overexpression of miR-17/20a, compared with siCtrl. Graph error bars indicate s.d. calculated on at least three independent experiments. * P <0.05 versus LNA-siCtrl ** P <0.05 versus siNanog. ( D ) Model illustrating the coordinated loop among Nanog, p53 and Trp53inp1, centred on miR-17-92 cluster. In NSC, miR-17-92 cluster is regulated by Nanog that is in turn controlled by Hh signalling and p53 . Additional activities of p53 are the direct repression of miR-17/92 cluster and Hh/Gli . In turn, miR-17 and miR-20a, members of miR-17-92 cluster, target and inhibit Trp53inp1 (this study) that inhibits stem cell self-renewal. Red double-arrow line shows the induction of Trp53inp1 by p53 and the backward positive regulation of p53 by Trp53inp1. For further details, see text and references herein.

Journal: The EMBO Journal

Article Title: microRNA-17-92 cluster is a direct Nanog target and controls neural stem cell through Trp53inp1

doi: 10.1038/emboj.2013.214

Figure Lengend Snippet: miR-17/20a and Trp53inp1 role in NSC self-renewal. ( A ) Bright-field images of secondary neurosphere-forming assay of NSC transfected with LNA-anti-miR-17/20a alone or in combination with siTrp53inp1 (scale bar, 50 mm). ( B ) Histogram shows the percentage of neurosphere-forming cells after single or combined LNA anti-miR, their combination and the association with siTrp53inp1. Bars represent the mean of three independent experiments ±s.d. * P <0.05 versus siCtrl ** P <0.05 versus LNA miR-17/20a. ( C ) Secondary neurosphere-forming assay after silencing of Nanog alone (siNanog) or in combination with siTrp53inp1 or overexpression of miR-17/20a, compared with siCtrl. Graph error bars indicate s.d. calculated on at least three independent experiments. * P <0.05 versus LNA-siCtrl ** P <0.05 versus siNanog. ( D ) Model illustrating the coordinated loop among Nanog, p53 and Trp53inp1, centred on miR-17-92 cluster. In NSC, miR-17-92 cluster is regulated by Nanog that is in turn controlled by Hh signalling and p53 . Additional activities of p53 are the direct repression of miR-17/92 cluster and Hh/Gli . In turn, miR-17 and miR-20a, members of miR-17-92 cluster, target and inhibit Trp53inp1 (this study) that inhibits stem cell self-renewal. Red double-arrow line shows the induction of Trp53inp1 by p53 and the backward positive regulation of p53 by Trp53inp1. For further details, see text and references herein.

Article Snippet: Antagomir-mediated miRNA knockdown was carried out using fluorescein-labelled LNA oligonucleotides (Exiqon, Vedbaek, Denmark; miR-17: code 426848-00, miR-20a: code 411929-08) or combination of these miRNAs and scrambled control (Exiqon mirCURY knockdown probe control A: code 199002-08) (Exiqon), transfected into NSC cells at a final concentration of 50 nM by Hiperfect reagent (Qiagen, Hilden, Germany).

Techniques: Neurosphere Assay, Transfection, Over Expression

Correlation coefficients between  miRNA  expression and independent variables in the WEA cohort according to Spearman.

Journal: Scientific Reports

Article Title: Circulating microRNA-197-3p as a potential biomarker for asbestos exposure

doi: 10.1038/s41598-021-03189-9

Figure Lengend Snippet: Correlation coefficients between miRNA expression and independent variables in the WEA cohort according to Spearman.

Article Snippet: Hsa-miR-197-3p concentrations were analyzed by qPCR techniques using the specific miRCURY LNA miRNA PCR Assay (Qiagen Cod.

Techniques: Expressing