�ݺ�ߣshows by User: manglam91

�ݺ�ߣshows by User: manglam91 / http://www.slideshare.net/images/logo.gif �ݺ�ߣshows by User: manglam91 / Fri, 23 Sep 2016 06:22:38 GMT �ݺ�ߣShare feed for �ݺ�ߣshows by User: manglam91 Advances in stem cell technology /slideshow/advances-in-stem-cell-technology/66330188 advancesinstemcell-160923062238
Stem cells are one of the important cells present in both plant and animals. these cells have ability to regenerate any part of the body work similarily as meristem cells in plant. The advances in the stem cell technology has open a new era in medical field. the advances in this technology has been presented here and their important application has been included in this present in this presentation.]]>
Stem cells are one of the important cells present in both plant and animals. these cells have ability to regenerate any part of the body work similarily as meristem cells in plant. The advances in the stem cell technology has open a new era in medical field. the advances in this technology has been presented here and their important application has been included in this present in this presentation.]]> Fri, 23 Sep 2016 06:22:38 GMT /slideshow/advances-in-stem-cell-technology/66330188 manglam91@slideshare.net(manglam91) Advances in stem cell technology manglam91 Stem cells are one of the important cells present in both plant and animals. these cells have ability to regenerate any part of the body work similarily as meristem cells in plant. The advances in the stem cell technology has open a new era in medical field. the advances in this technology has been presented here and their important application has been included in this present in this presentation. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/advancesinstemcell-160923062238-thumbnail.jpg?width=120&height=120&fit=bounds" /> Stem cells are one of the important cells present in both plant and animals. these cells have ability to regenerate any part of the body work similarily as meristem cells in plant. The advances in the stem cell technology has open a new era in medical field. the advances in this technology has been presented here and their important application has been included in this present in this presentation.

Advances in stem cell technology from MANGLAM ARYA

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0 Micro and Nanofludics /manglam91/micro-and-nanofludics manjesh-microfluids-150518064121-lva1-app6891
this slide will to know about micro and nanofludic- what it is? and what are all its application in nanobiotechnology and biotechnology.]]>
this slide will to know about micro and nanofludic- what it is? and what are all its application in nanobiotechnology and biotechnology.]]> Mon, 18 May 2015 06:41:21 GMT /manglam91/micro-and-nanofludics manglam91@slideshare.net(manglam91) Micro and Nanofludics manglam91 this slide will to know about micro and nanofludic- what it is? and what are all its application in nanobiotechnology and biotechnology. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/manjesh-microfluids-150518064121-lva1-app6891-thumbnail.jpg?width=120&height=120&fit=bounds" /> this slide will to know about micro and nanofludic- what it is? and what are all its application in nanobiotechnology and biotechnology.

Micro and Nanofludics from MANGLAM ARYA

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0 Single Nucleotide Polymorphism Genotyping Using �Kompetitive Allele Specific PCR (KASP) /slideshow/kasp-47154996/47154996 kasp-150418225932-conversion-gate01
Single Nucleotide Polymorphism Single nucleotide polymorphism (SNP) refers to a single base change in a DNA sequence SNP: Commonly biallelic Two types(Based on presence in genome) Synonymus Non-synonymus SNPs have largely replaced simple sequence repeats (SSRs) Advantage of using SNPs Low assay cost High genomic abundance Locus specificity co-dominant inheritance Simple documentation Potential for high-throughput Analysis Relatively low genotyping error rates SNP genotyping platforms BeadXpressTM,GoldenGateTM and Infinium from Illumina GeneChipTM and GenFlexTM Tag array from Affimetrix SNaPshotTM and TaqManTM from the Applied Biosystems SNPWaveTM from KeyGene iPLEX GoldTM Assay and Mass-RRAYTM from Sequonome Variables to be considered Throughput Data turnaround Time Ease of use Performance (sensitivity, reliability, reproducibility, and accuracy), Flexibility (genotyping few samples with many snps or many samples with few snps), Number of markers generated per run (uniplex versus multiplex assay capability) Assay development requirements and genotyping cost per sample or data point. KASP KBioscience Competitive Allele-Specific PCR Homogenous, Fluorescence-based genotyping technology, based on Allele-specific oligo extension (primer) Fluorescence resonance energy transfer KASP Applications Genotyping a wide range of species for various purposes. KASP for Quality analysis, QTL mapping, MARS, and allele mining Quality Control Analysis QC analysis should be done for two reasons by genotyping the parents and F1s with the same subset of SNPs, in order to confirm if F1s contains true-to-type alleles from their parents check the genetic purity of the inbred parents. F1s with true-to-type parental alleles for at least 90 % of the SNPs that were polymorphic between the parents should be advanced, while those with less than 10 % nonparental alleles should be discarded. QTL Mapping QTL mapping identifies a subset of markers that are significantly associated with one or more QTL influencing the expression of the trait of interest. 1) Select or develop a bi-parental mapping population. 2) Phenotype the population for a trait under greenhouse or field conditions. 3) Choose a molecular marking system – genotype parents of the mapping population and F1s with large numbers of markers, then select 200-400 markers exhibiting polymorphism between the parents. 4) Choose a genotyping approach, then generate molecular data for polymorphic markers 5) Identify the molecular markers associated with major QTL using statistical programs. Large-scale allele mining Allele mining is a promising approach to dissecting naturally occurring allelic variation at candidate genes controlling key agronomic traits. KASP platform at CIMMYT has been used for the systematic mining of large germplasm collections for specific functional polymorphisms. SNPs or small indels that]]>
Single Nucleotide Polymorphism Single nucleotide polymorphism (SNP) refers to a single base change in a DNA sequence SNP: Commonly biallelic Two types(Based on presence in genome) Synonymus Non-synonymus SNPs have largely replaced simple sequence repeats (SSRs) Advantage of using SNPs Low assay cost High genomic abundance Locus specificity co-dominant inheritance Simple documentation Potential for high-throughput Analysis Relatively low genotyping error rates SNP genotyping platforms BeadXpressTM,GoldenGateTM and Infinium from Illumina GeneChipTM and GenFlexTM Tag array from Affimetrix SNaPshotTM and TaqManTM from the Applied Biosystems SNPWaveTM from KeyGene iPLEX GoldTM Assay and Mass-RRAYTM from Sequonome Variables to be considered Throughput Data turnaround Time Ease of use Performance (sensitivity, reliability, reproducibility, and accuracy), Flexibility (genotyping few samples with many snps or many samples with few snps), Number of markers generated per run (uniplex versus multiplex assay capability) Assay development requirements and genotyping cost per sample or data point. KASP KBioscience Competitive Allele-Specific PCR Homogenous, Fluorescence-based genotyping technology, based on Allele-specific oligo extension (primer) Fluorescence resonance energy transfer KASP Applications Genotyping a wide range of species for various purposes. KASP for Quality analysis, QTL mapping, MARS, and allele mining Quality Control Analysis QC analysis should be done for two reasons by genotyping the parents and F1s with the same subset of SNPs, in order to confirm if F1s contains true-to-type alleles from their parents check the genetic purity of the inbred parents. F1s with true-to-type parental alleles for at least 90 % of the SNPs that were polymorphic between the parents should be advanced, while those with less than 10 % nonparental alleles should be discarded. QTL Mapping QTL mapping identifies a subset of markers that are significantly associated with one or more QTL influencing the expression of the trait of interest. 1) Select or develop a bi-parental mapping population. 2) Phenotype the population for a trait under greenhouse or field conditions. 3) Choose a molecular marking system – genotype parents of the mapping population and F1s with large numbers of markers, then select 200-400 markers exhibiting polymorphism between the parents. 4) Choose a genotyping approach, then generate molecular data for polymorphic markers 5) Identify the molecular markers associated with major QTL using statistical programs. Large-scale allele mining Allele mining is a promising approach to dissecting naturally occurring allelic variation at candidate genes controlling key agronomic traits. KASP platform at CIMMYT has been used for the systematic mining of large germplasm collections for specific functional polymorphisms. SNPs or small indels that]]> Sat, 18 Apr 2015 22:59:32 GMT /slideshow/kasp-47154996/47154996 manglam91@slideshare.net(manglam91) Single Nucleotide Polymorphism Genotyping Using �Kompetitive Allele Specific PCR (KASP) manglam91 Single Nucleotide Polymorphism Single nucleotide polymorphism (SNP) refers to a single base change in a DNA sequence SNP: Commonly biallelic Two types(Based on presence in genome) Synonymus Non-synonymus SNPs have largely replaced simple sequence repeats (SSRs) Advantage of using SNPs Low assay cost High genomic abundance Locus specificity co-dominant inheritance Simple documentation Potential for high-throughput Analysis Relatively low genotyping error rates SNP genotyping platforms BeadXpressTM,GoldenGateTM and Infinium from Illumina GeneChipTM and GenFlexTM Tag array from Affimetrix SNaPshotTM and TaqManTM from the Applied Biosystems SNPWaveTM from KeyGene iPLEX GoldTM Assay and Mass-RRAYTM from Sequonome Variables to be considered Throughput Data turnaround Time Ease of use Performance (sensitivity, reliability, reproducibility, and accuracy), Flexibility (genotyping few samples with many snps or many samples with few snps), Number of markers generated per run (uniplex versus multiplex assay capability) Assay development requirements and genotyping cost per sample or data point. KASP KBioscience Competitive Allele-Specific PCR Homogenous, Fluorescence-based genotyping technology, based on Allele-specific oligo extension (primer) Fluorescence resonance energy transfer KASP Applications Genotyping a wide range of species for various purposes. KASP for Quality analysis, QTL mapping, MARS, and allele mining Quality Control Analysis QC analysis should be done for two reasons by genotyping the parents and F1s with the same subset of SNPs, in order to confirm if F1s contains true-to-type alleles from their parents check the genetic purity of the inbred parents. F1s with true-to-type parental alleles for at least 90 % of the SNPs that were polymorphic between the parents should be advanced, while those with less than 10 % nonparental alleles should be discarded. QTL Mapping QTL mapping identifies a subset of markers that are significantly associated with one or more QTL influencing the expression of the trait of interest. 1) Select or develop a bi-parental mapping population. 2) Phenotype the population for a trait under greenhouse or field conditions. 3) Choose a molecular marking system – genotype parents of the mapping population and F1s with large numbers of markers, then select 200-400 markers exhibiting polymorphism between the parents. 4) Choose a genotyping approach, then generate molecular data for polymorphic markers 5) Identify the molecular markers associated with major QTL using statistical programs. Large-scale allele mining Allele mining is a promising approach to dissecting naturally occurring allelic variation at candidate genes controlling key agronomic traits. KASP platform at CIMMYT has been used for the systematic mining of large germplasm collections for specific functional polymorphisms. SNPs or small indels that <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/kasp-150418225932-conversion-gate01-thumbnail.jpg?width=120&height=120&fit=bounds" /> Single Nucleotide Polymorphism Single nucleotide polymorphism (SNP) refers to a single base change in a DNA sequence SNP: Commonly biallelic Two types(Based on presence in genome) Synonymus Non-synonymus SNPs have largely replaced simple sequence repeats (SSRs) Advantage of using SNPs Low assay cost High genomic abundance Locus specificity co-dominant inheritance Simple documentation Potential for high-throughput Analysis Relatively low genotyping error rates SNP genotyping platforms BeadXpressTM,GoldenGateTM and Infinium from Illumina GeneChipTM and GenFlexTM Tag array from Affimetrix SNaPshotTM and TaqManTM from the Applied Biosystems SNPWaveTM from KeyGene iPLEX GoldTM Assay and Mass-RRAYTM from Sequonome Variables to be considered Throughput Data turnaround Time Ease of use Performance (sensitivity, reliability, reproducibility, and accuracy), Flexibility (genotyping few samples with many snps or many samples with few snps), Number of markers generated per run (uniplex versus multiplex assay capability) Assay development requirements and genotyping cost per sample or data point. KASP KBioscience Competitive Allele-Specific PCR Homogenous, Fluorescence-based genotyping technology, based on Allele-specific oligo extension (primer) Fluorescence resonance energy transfer KASP Applications Genotyping a wide range of species for various purposes. KASP for Quality analysis, QTL mapping, MARS, and allele mining Quality Control Analysis QC analysis should be done for two reasons by genotyping the parents and F1s with the same subset of SNPs, in order to confirm if F1s contains true-to-type alleles from their parents check the genetic purity of the inbred parents. F1s with true-to-type parental alleles for at least 90 % of the SNPs that were polymorphic between the parents should be advanced, while those with less than 10 % nonparental alleles should be discarded. QTL Mapping QTL mapping identifies a subset of markers that are significantly associated with one or more QTL influencing the expression of the trait of interest. 1) Select or develop a bi-parental mapping population. 2) Phenotype the population for a trait under greenhouse or field conditions. 3) Choose a molecular marking system – genotype parents of the mapping population and F1s with large numbers of markers, then select 200-400 markers exhibiting polymorphism between the parents. 4) Choose a genotyping approach, then generate molecular data for polymorphic markers 5) Identify the molecular markers associated with major QTL using statistical programs. Large-scale allele mining Allele mining is a promising approach to dissecting naturally occurring allelic variation at candidate genes controlling key agronomic traits. KASP platform at CIMMYT has been used for the systematic mining of large germplasm collections for specific functional polymorphisms. SNPs or small indels that

Single Nucleotide Polymorphism Genotyping Using Kompetitive Allele Specific PCR (KASP) from MANGLAM ARYA

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0 micropropagation in dendribium /slideshow/new-microsoft-office-power-point-presentation-2-42888453/42888453 newmicrosoftofficepowerpointpresentation2-141219234135-conversion-gate01
Dendrobium Family – Orchidaceae Exhibits a vast diversity in vegetative and floral characteristics 1,600 Dendrobium species are recognized worldwide High value of crop – for flower and medicinal purpose D. husohanense- Anti-tumor and Anti- inflammatry D. longicornu - used to treat fever and coughs Micropropagation Seeds are minute and lack endosperm Micropropagation has been achieved using Shoot tip culture Seed culture (Immature and mature embryo) Auxiliary Bud culture Pseudobulb segment culture Shoot Tip culture Sterlization of Explant Shoot tips(0.5–0.8 cm) harvested from mother plants carefully washed in distilled water surface decontaminated with 0.1% streptomycin (20 s) 70% (v/v) ethanol (50 s) and 0.1% (w/v) HgCl2 (2 min) Thoroughly rinsed with sterilized distilled water Media Subculturing Micropropagation of Dendrobium From Pseudobulb segment Regeneration from Pseudobulb Segment Cultures Pseudobulb segments of about 0.5-1.0 cm excised from the 1 year old in vitro raised seedlings Any leaves or roots, if present, were removed from the segments prior to inoculation Each segment had one or two axillary buds. Single pseudobulb segment was cultured in test tubes (25 mm × 150 mm), each containing 12 mL half-strength MS basal medium supplemented with BAP 1.0 mg L-1 individually or in combination with NAA at 1 mg L-1 The medium was solidified with 4 g L-1 agar Rooting of Regenerated Shoots (Pseudobulbs) Small clumps of shoots having 2-3 pseudobulbs (3-4 cm in length) were cultured in test tubes (25 mm × 150 mm) Each containing 12 mL half-strength MS basal medium supplemented with or without 1.0 mg L-1 IAA or IBA or NAA. The cultures were incubated for 3 months under the conditions as described above. The pH was adjusted to 5.8 before autoclaving at 121°C, 15 lb in-2 for 15 min. Micropropagation of Dendrobium From Auxiliary bud Stem (1–2 cm long), each comprising a node and axillary bud are used as explant- wash in running tape water for 15-20 minute Surface sterilization with- - 10 % (v/v) NaClO solution for 10 minute - 0.1 % (w/v) HgCl2 for 2 min - washing 5–6 times with sterilized distilled water The explants were shortened to 3–4 mm after the removal of leaves, dry sheaths and other external tissues Micropropagation of Dendrobium from immature seeds Capsules collected from hand-pollinated plants after 8–14 wk of pollination Surface-disinfected in 70% ethanol for 30 s, followed by 1.0% sodium hypochlorite with two drops of Tween 20 per 100 ml for 10 min and rinsed five times with sterile distilled water After sterilization, the c]]>
Dendrobium Family – Orchidaceae Exhibits a vast diversity in vegetative and floral characteristics 1,600 Dendrobium species are recognized worldwide High value of crop – for flower and medicinal purpose D. husohanense- Anti-tumor and Anti- inflammatry D. longicornu - used to treat fever and coughs Micropropagation Seeds are minute and lack endosperm Micropropagation has been achieved using Shoot tip culture Seed culture (Immature and mature embryo) Auxiliary Bud culture Pseudobulb segment culture Shoot Tip culture Sterlization of Explant Shoot tips(0.5–0.8 cm) harvested from mother plants carefully washed in distilled water surface decontaminated with 0.1% streptomycin (20 s) 70% (v/v) ethanol (50 s) and 0.1% (w/v) HgCl2 (2 min) Thoroughly rinsed with sterilized distilled water Media Subculturing Micropropagation of Dendrobium From Pseudobulb segment Regeneration from Pseudobulb Segment Cultures Pseudobulb segments of about 0.5-1.0 cm excised from the 1 year old in vitro raised seedlings Any leaves or roots, if present, were removed from the segments prior to inoculation Each segment had one or two axillary buds. Single pseudobulb segment was cultured in test tubes (25 mm × 150 mm), each containing 12 mL half-strength MS basal medium supplemented with BAP 1.0 mg L-1 individually or in combination with NAA at 1 mg L-1 The medium was solidified with 4 g L-1 agar Rooting of Regenerated Shoots (Pseudobulbs) Small clumps of shoots having 2-3 pseudobulbs (3-4 cm in length) were cultured in test tubes (25 mm × 150 mm) Each containing 12 mL half-strength MS basal medium supplemented with or without 1.0 mg L-1 IAA or IBA or NAA. The cultures were incubated for 3 months under the conditions as described above. The pH was adjusted to 5.8 before autoclaving at 121°C, 15 lb in-2 for 15 min. Micropropagation of Dendrobium From Auxiliary bud Stem (1–2 cm long), each comprising a node and axillary bud are used as explant- wash in running tape water for 15-20 minute Surface sterilization with- - 10 % (v/v) NaClO solution for 10 minute - 0.1 % (w/v) HgCl2 for 2 min - washing 5–6 times with sterilized distilled water The explants were shortened to 3–4 mm after the removal of leaves, dry sheaths and other external tissues Micropropagation of Dendrobium from immature seeds Capsules collected from hand-pollinated plants after 8–14 wk of pollination Surface-disinfected in 70% ethanol for 30 s, followed by 1.0% sodium hypochlorite with two drops of Tween 20 per 100 ml for 10 min and rinsed five times with sterile distilled water After sterilization, the c]]> Fri, 19 Dec 2014 23:41:35 GMT /slideshow/new-microsoft-office-power-point-presentation-2-42888453/42888453 manglam91@slideshare.net(manglam91) micropropagation in dendribium manglam91 Dendrobium Family – Orchidaceae Exhibits a vast diversity in vegetative and floral characteristics 1,600 Dendrobium species are recognized worldwide High value of crop – for flower and medicinal purpose D. husohanense- Anti-tumor and Anti- inflammatry D. longicornu - used to treat fever and coughs Micropropagation Seeds are minute and lack endosperm Micropropagation has been achieved using Shoot tip culture Seed culture (Immature and mature embryo) Auxiliary Bud culture Pseudobulb segment culture Shoot Tip culture Sterlization of Explant Shoot tips(0.5–0.8 cm) harvested from mother plants carefully washed in distilled water surface decontaminated with 0.1% streptomycin (20 s) 70% (v/v) ethanol (50 s) and 0.1% (w/v) HgCl2 (2 min) Thoroughly rinsed with sterilized distilled water Media Subculturing Micropropagation of Dendrobium From Pseudobulb segment Regeneration from Pseudobulb Segment Cultures Pseudobulb segments of about 0.5-1.0 cm excised from the 1 year old in vitro raised seedlings Any leaves or roots, if present, were removed from the segments prior to inoculation Each segment had one or two axillary buds. Single pseudobulb segment was cultured in test tubes (25 mm × 150 mm), each containing 12 mL half-strength MS basal medium supplemented with BAP 1.0 mg L-1 individually or in combination with NAA at 1 mg L-1 The medium was solidified with 4 g L-1 agar Rooting of Regenerated Shoots (Pseudobulbs)� Small clumps of shoots having 2-3 pseudobulbs (3-4 cm in length) were cultured in test tubes (25 mm × 150 mm) Each containing 12 mL half-strength MS basal medium supplemented with or without 1.0 mg L-1 IAA or IBA or NAA. The cultures were incubated for 3 months under the conditions as described above. The pH was adjusted to 5.8 before autoclaving at 121°C, 15 lb in-2 for 15 min. Micropropagation of Dendrobium From Auxiliary bud Stem (1–2 cm long), each comprising a node and axillary bud are used as explant- wash in running tape water for 15-20 minute Surface sterilization with- - 10 % (v/v) NaClO solution for 10 minute - 0.1 % (w/v) HgCl2 for 2 min - washing 5–6 times with sterilized distilled water The explants were shortened to 3–4 mm after the removal of leaves, dry sheaths and other external tissues Micropropagation of Dendrobium from immature seeds Capsules collected from hand-pollinated plants after 8–14 wk of pollination Surface-disinfected in 70% ethanol for 30 s, followed by 1.0% sodium hypochlorite with two drops of Tween 20 per 100 ml for 10 min and rinsed five times with sterile distilled water After sterilization, the c <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/newmicrosoftofficepowerpointpresentation2-141219234135-conversion-gate01-thumbnail.jpg?width=120&height=120&fit=bounds" /> Dendrobium Family – Orchidaceae Exhibits a vast diversity in vegetative and floral characteristics 1,600 Dendrobium species are recognized worldwide High value of crop – for flower and medicinal purpose D. husohanense- Anti-tumor and Anti- inflammatry D. longicornu - used to treat fever and coughs Micropropagation Seeds are minute and lack endosperm Micropropagation has been achieved using Shoot tip culture Seed culture (Immature and mature embryo) Auxiliary Bud culture Pseudobulb segment culture Shoot Tip culture Sterlization of Explant Shoot tips(0.5–0.8 cm) harvested from mother plants carefully washed in distilled water surface decontaminated with 0.1% streptomycin (20 s) 70% (v/v) ethanol (50 s) and 0.1% (w/v) HgCl2 (2 min) Thoroughly rinsed with sterilized distilled water Media Subculturing Micropropagation of Dendrobium From Pseudobulb segment Regeneration from Pseudobulb Segment Cultures Pseudobulb segments of about 0.5-1.0 cm excised from the 1 year old in vitro raised seedlings Any leaves or roots, if present, were removed from the segments prior to inoculation Each segment had one or two axillary buds. Single pseudobulb segment was cultured in test tubes (25 mm × 150 mm), each containing 12 mL half-strength MS basal medium supplemented with BAP 1.0 mg L-1 individually or in combination with NAA at 1 mg L-1 The medium was solidified with 4 g L-1 agar Rooting of Regenerated Shoots (Pseudobulbs)� Small clumps of shoots having 2-3 pseudobulbs (3-4 cm in length) were cultured in test tubes (25 mm × 150 mm) Each containing 12 mL half-strength MS basal medium supplemented with or without 1.0 mg L-1 IAA or IBA or NAA. The cultures were incubated for 3 months under the conditions as described above. The pH was adjusted to 5.8 before autoclaving at 121°C, 15 lb in-2 for 15 min. Micropropagation of Dendrobium From Auxiliary bud Stem (1–2 cm long), each comprising a node and axillary bud are used as explant- wash in running tape water for 15-20 minute Surface sterilization with- - 10 % (v/v) NaClO solution for 10 minute - 0.1 % (w/v) HgCl2 for 2 min - washing 5–6 times with sterilized distilled water The explants were shortened to 3–4 mm after the removal of leaves, dry sheaths and other external tissues Micropropagation of Dendrobium from immature seeds Capsules collected from hand-pollinated plants after 8–14 wk of pollination Surface-disinfected in 70% ethanol for 30 s, followed by 1.0% sodium hypochlorite with two drops of Tween 20 per 100 ml for 10 min and rinsed five times with sterile distilled water After sterilization, the c

micropropagation in dendribium from MANGLAM ARYA

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0 Dna replication /slideshow/dna-replication-41555427/41555427 dnareplicationmanglam-141114061943-conversion-gate01
this presentation help the students to learn about DNA replication in prokaryote and eukaryote .]]>
this presentation help the students to learn about DNA replication in prokaryote and eukaryote .]]> Fri, 14 Nov 2014 06:19:43 GMT /slideshow/dna-replication-41555427/41555427 manglam91@slideshare.net(manglam91) Dna replication manglam91 this presentation help the students to learn about DNA replication in prokaryote and eukaryote . <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/dnareplicationmanglam-141114061943-conversion-gate01-thumbnail.jpg?width=120&height=120&fit=bounds" /> this presentation help the students to learn about DNA replication in prokaryote and eukaryote .

Dna replication from MANGLAM ARYA

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0 https://public.slidesharecdn.com/v2/images/profile-picture.png https://cdn.slidesharecdn.com/ss_thumbnails/advancesinstemcell-160923062238-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/advances-in-stem-cell-technology/66330188 Advances in stem cell ... https://cdn.slidesharecdn.com/ss_thumbnails/manjesh-microfluids-150518064121-lva1-app6891-thumbnail.jpg?width=320&height=320&fit=bounds manglam91/micro-and-nanofludics Micro and Nanofludics https://cdn.slidesharecdn.com/ss_thumbnails/kasp-150418225932-conversion-gate01-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/kasp-47154996/47154996 Single Nucleotide Poly...