Overview of Hi-Gx360

Hi-Gx360 enables companies to improve their genomics and bioinformatics workflow, ensuring a smooth trip from sample to insights.

Hi-Gx360® sequencing and bioinformatics services

Sequencing and bioinformatics services with the Hi-Gx360

Image Credit: HiMedia Laboratories Pvt. Ltd.

HiMedia stands for:

  • High-quality data production for many sequencing applications
  • No hidden fees
    • Standard vector primers or universal gene primers already available with us can be offered (only for sequencing services) at no additional expense
    • No additional price for difficult-to-sequence templates
    • Help debug sequencing tasks at no additional cost
  • Completely customized solutions that meet the project requirements (based on prior discussion)
  • Analytic pipelines are functionally evaluated, optimized, and verified utilizing open source technologies
  • Experts in bioinformatics and sequencing provide direct support
  • Shared knowledge base and resources for user empowerment

State-of-art Hi-Gx360® lab

Sequencing and bioinformatics services with the Hi-Gx360

Sequencing and bioinformatics services with the Hi-Gx360

Image Credit: HiMedia Laboratories Pvt. Ltd. 

Sanger sequencing applications

  • A very accurate 'chain termination-based' 'first generation' DNA sequencing technique
  • The gold standard for benchmarking all other sequencing methods, including NGS
  • Confirm sequence variants or fill ‘gaps’ in genomic areas identified by NGS
  • Predesigned identification service under Isolate-to-Identity, encompassing all organisms
  • Detailed reports always contain .ab1 files and other relevant information
  • Standard vector primers and universal gene markers included at no cost (only for sequencing services)
  • Gene sequence-based phylogenetic analysis service
  • Stuck with NCBI GenBank submissions, connect with HiMedia

Sequencing and bioinformatics services with the Hi-Gx360

Image Credit: HiMedia Laboratories Pvt. Ltd.

Sanger sequencing services

Source: HiMedia Laboratories Pvt. Ltd.

Description   Service Codes
Single pass sequencing ~700 bp purified PCR/Plasmid MBS101
unpurified PCR/Plasmid MBS102
Single-strand F & R primer sequencing ~1200 bp purified PCR/Plasmid MBS103
unpurified PCR/Plasmid MBS104
Single strand F&R primer sequencing & BLAST analysis ~1200 bp unpurified PCR/Plasmid MBS104A
Double pass both strands 1.5-2 kb purified PCR/Plasmid MBS105
unpurified PCR/Plasmid MBS106
96-well plate single pass sequencing ~700 bp purified PCR/Plasmid MBS107
unpurified PCR/Plasmid MBS108
Primer walking (upto 2 kb)   MBS121
Primer walking (upto 5 kb) with DNA extraction   MBS121A
Ready-to-Run 96-well plate single pass sequencing (~700 bp)   MBS122
gDNA-to-Sequence 96-well plate single pass sequencing (~700 bp)   MBS123
gDNA-to-Sequence 96-well plate F & R primer sequencing (~1200 bp)   MBS124

 

Supplemental services

Only available in conjunction with other service codes, not independently.

Source: HiMedia Laboratories Pvt. Ltd.

Description Service Codes
Agarose Gel Extraction MBS301
Plasmid DNA Isolation MBS302
Purification of PCR Products MBS303
Agarose Gel-based QC MBS305

 

Identification of organisms (Isolate-to-Identity)

Sequencing and bioinformatics services with the Hi-Gx360

Image Credit: HiMedia Laboratories Pvt. Ltd.

Identification services

Source: HiMedia Laboratories Pvt. Ltd.

Description   Service Codes
Bacterial/Archaeal 16S rRNA-based Identification From Genomic DNA  MBS109
From Pure Isolate  MBS110
16s rRNA-based partial Identification
(gDNA to BLAST, ~700 bp single pass)
Does not include phylogenetic analysis (MBS020). MBS109A
16s rRNA-based partial Identification
(gDNA to BLAST, ~1200 bp single pass)
Does not include phylogenetic analysis (MBS020). MBS109B
Fungal ITS-based Identification From Genomic DNA MBS111
From Pure Isolates MBS112
Fungal 18S rRNA-based Identification From Genomic DNA MBS113
From Pure Isolates MBS114
Algal 18S rRNA-based Identification From Genomic DNA MBS115
From Pure Isolates MBS116
Algal 23S rRNA-based Identification From Genomic DNA MBS117
From Pure Isolates MBS118

 

NABL accredited services

Source: HiMedia Laboratories Pvt. Ltd.

Description Service Codes
Hi-Gx360® Microbial Identification by 16S rRNA gene sequencing from genomic DNA MBS409
Hi-Gx360® Microbial Identification by 16S rRNA gene sequencing from pure isolate MBS410
Hi-Gx360® Fungal Identification by ITS sequencing from genomic DNA MBS411
Hi-Gx360® Fungal Identification by ITS sequencing from Pure Isolates MBS412
Hi-Gx360® Fungal Identification by 18S rRNA gene sequencing from genomic DNA MBS413
Hi-Gx360® Fungal Identification by 18S rRNA gene sequencing from Pure Isolates MBS414

 


Next generation sequencing

Whole genome sequencing applications

Whole Genome Sequencing (WGS) has facilitated the thorough analysis of the complete genomic sequences of various organisms. This data is essential for gaining insights into the functional and evolutionary backgrounds of these organisms, as well as for detecting mutations and genetic variations linked to genetic disorders, cancer progression, disease outbreaks, and the emergence of strains with new pathogenic characteristics.

HiGx360® generates all the information required to comprehend the activities of all expected genes present in the organism in detail using a read-to-annotation technique. Since assembled genomes might not be entirely complete, one of the several long read sequencing methods can be used to fill in additional gaps.

  • Sequence close relatives of reference-organisms or entirely novel organisms (de-novo)
  • Obtain high-resolution and precise genomic characterization utilizing 2×150 or 2× 300 bp readings
  • Data supplied with interactive QC report
  • Get personalized bioinformatics analysis, including raw sequence reads, assembled contigs, and scaffolds
  • Choose from basic or advanced bioinformatics

Recommendations

Source: HiMedia Laboratories Pvt. Ltd.

  Resequencing De-novo Sequencing
Depth/Coverage 50X - 100X >100X
Read length chemistry 2x75 to 2x300
Sample Requirements Minimum quantity 0.5 μg, Minimum concentration = 20 ng/μl (Qubit), A260/280 = 1.8 - 2.0

 

Deliverables

  • Run information, Statistics of raw data & FASTQ file
  • Reference Genome Mapping files/ De-novo Genome Mapping files, Functional Annotations, Gene predictions, Gene annotations, Pangenome analysis
  • Advanced analysis customized to the project needs

WGS services

Source: HiMedia Laboratories Pvt. Ltd.

Description Service Codes
Whole Genome Sequencing (0.5 Gb Data) MBS201
Whole Genome Sequencing (1 Gb Data)  MBS201-1G
Whole Genome Sequencing (2 Gb Data)  MBS201-2G
Whole Genome Sequencing (4 Gb Data) MBS201-4G
Whole Genome Sequencing (6 Gb Data)  MBS201-6G
Whole Genome Sequencing (8 Gb Data) MBS201-8G
Whole Genome Sequencing (10 Gb Data) MBS201-10G
Whole Genome Sequencing (12 Gb Data)  MBS201-12G
Whole Genome Sequencing (16 Gb Data) MBS201-16G
Whole Genome Sequencing (20 Gb Data) MBS201-20G
Whole Genome Sequencing (25 Gb data) MBS201-25G
Whole Genome Sequencing (30 Gb data) MBS201-30G
Whole Genome Sequencing (50 Gb data) MBS201-50G
Whole Genome Sequencing (60 Gb data) MBS201-60G
Whole Genome Sequencing (100 Gb data) MBS201-100G
Whole Genome Sequencing (30 Mb data, eg., Mycoplasma @50X) MBS201-30M
Whole Genome Sequencing (250 Mb data, eg., Bacteria @50X) MBS201-250M
Whole Genome Sequencing (Virus) (0.5GB) MBS202
Whole Genome Sequencing (Virus, 10Kb @ 100X) MBS202-1K
Whole Genome Sequencing (Virus, 20Kb @ 100X) MBS202-2K
Whole Genome Sequencing (Virus, 50Kb @ 100X) MBS202-5K
COVIDSeq on MiSeq (per sample for 95 samples) MBS222

* Gb - Gigabases, Mb-Millionbases, KB - Kilobases

Whole exome sequencing applications

The human genome comprises 180,000 coding regions, representing 1.7% of its total structure. Approximately 85% of genetic-based human diseases arise from anomalies within these coding regions. The focused sequencing of these genomic areas is referred to as whole exome sequencing (WES). Compared to sequencing the entire human genome, exome sequencing offers a more economical alternative.

This sequencing technique employs a targeted capture strategy, utilizing biotinylated probes that are directed toward the coding regions of the fragmented human genome. These probes facilitate the capture and isolation of specific genomic segments using streptavidin-coated beads. The resulting fragments are then sequenced using the NextSeq™ 2000 platform. This approach achieves a significant enhancement in coverage, providing a 100-fold increase in the relevant areas of the genome.

  • More affordable and widely accessible
  • Sequencing coverage on target upto 30×
  • Finding coding SNP variations with the same level of sensitivity as whole-genome sequencing
  • Compared to whole-genome sequencing, a smaller data set allows for quicker and simpler analysis
  • Standard sequencing coverage ≥ 50×; cancer sample ≥ 100×. More SNPs can be gained by increasing the coverage
  • Exome enrichment options and affordable library preparation

Exome sequencing recommendations

Source: HiMedia Laboratories Pvt. Ltd.

  Whole Exome Sequencing Cancer Specific and/or Rare Variant Detection
Depth/Coverage 100-300X 500–1000X
Read length chemistry 2x75 to 2x150
Capture Region
  • 34 Mb target region
  • 415,115 oligonucleotide probes
  • 19433 genes
Sample Requirements Required quantity 1.0 – 0.5 μg, Minimum concentration = 20 ng/μl (Qubit), A260/280 = 1.8 - 2.0

 

Deliverables

  • SNPs and InDels calling, Variant annotation, SNVs concordance, Tumor-Normal paired analysis
  • Run information, Statistics of raw data & FASTQ/VCF files
  • Mapping statistics, Statistics of sequencing reads

WES services

Source: HiMedia Laboratories Pvt. Ltd.

Description Service Codes
Whole Exome Sequencing MBS212-45M
Whole Exome Sequencing                                 MBS212-64M

* Gb - Gigabases, Mb-Millionbases, KB - Kilobases


Metagenomics and microbiome applications

Life on Earth depends on microorganisms. The functional potential of microbial communities can be inferred from descriptive metrics such as the metagenome, which is the collection of genes and genomes of the microbiota, and the microbiota, which is the collection of microorganisms existing in a certain environment.

A more thorough knowledge of hypothesis testing is made possible by microbiome interactions, which relate to the overall habitat, including the microbes, their genomes, and the surrounding environmental factors. The Hi-Gx360® NGS service allows users to:

  • Sequence a set of microbiota genes or genomes in any sample
  • Sequence the 16S and ITS marker, as well as additional genomic regions and marker genes
  • Learn about the functional importance of microbial diversity in detail
  • Use in-depth sequencing to find microbial species that are scarce

Metagenome sequencing

Shotgun metagenomics is a reliable method for studying environmental, agricultural, and human microbiomes, identifying and monitoring pathogens, and tracking antimicrobial resistance genes. Some of the most popular uses are:

  • Discovery of novel enzymes and metabolic pathways
  • Relative abundance analysis of microbial communities
  • Identification and classification of microbial communities
  • Novel biomarker discoveries
  • De-novo assembly and characterizations of novel genomes

Amplicon-based microbiome sequencing

  • A promising method for high-throughput phylogenetic study of communities of microbes
  • Based on phylogenetic marker genes: 16S rRNA genes, and ITS region
  • Enables the characterization of taxonomic diversity and species identification.
  • Provides detailed insight into the genus and species

Advantages of amplicon-based phylogenetic gene marker sequencing

  • Marker genes are omnipresent
  • Marker genes are relatively abundant compared to other genes
  • Measures phylogenetic connections between various taxa
  • Easily determine the relative abundance of microbial communities
  • Highly cost-effective

Recommendations

Source: HiMedia Laboratories Pvt. Ltd.

  Shotgun Metagenome Amplicon-based MiCrobiome
Objective
  • Discovery metagenomics
  • Relative abundance of microbial communities
  • Metagenome assembled genome sequencing
Taxonomic profiling
Reads per sample 25-500 Million paired end reads* Over 1 Lakh paired end reads*
Read length chemistry 1x150 to 2x300
Sample Requirements Minimum Quantity 1 μg, Minimum Concentration = 50 ng/μl (Qubit), OD 260/280=1.8-2.0

 

Deliverables

  • Run information, Statistics of raw data and FASTQ files
  • Taxonomic profiles, Functional Annotations, Metagenome assembled genomes (MAGs)
  • Advanced analysis customized to the project needs

Shotgun-metagenome based services

Source: HiMedia Laboratories Pvt. Ltd.

Description   Service Codes
Metagenome sequencing (soil/ sediment/water) (5 Gb Data) MBS213-5G
(10 Gb Data) MBS213-10G
(15 Gb Data) MBS213-15G
(20 Gb Data) MBS213-20G
Metagenome sequencing (Clinical) (1 Gb Data) MBS214-1G
(5 Gb Data) MBS214-5G
(10 Gb Data) MBS214-10G
(15 Gb Data) MBS214-15G
(20 Gb Data) MBS214-20G
Metagenome sequencing Environmental DNA (eDNA) (5 Gb Data) MBS215-5G
(10 Gb Data) MBS215-10G
(15 Gb Data) MBS215-15G
(20 Gb Data) MBS215-20G

* Gb - Gigabases, Mb-Millionbases, KB - Kilobases

Amplicon-based microbiome services

Source: HiMedia Laboratories Pvt. Ltd.

Description   Service Codes
Microbiome sequencing from Community DNA (16S) (2.5 lakh PE reads) MBS203-2L
(5 lakh PE reads) MBS203-5L
(10 lakh PE reads) MBS203-10L
Microbiome sequencing from Insect/Food sample (16S) (2.5 lakh PE reads) MBS204-2L
(5 lakh PE reads) MBS204-5L
Microbiome sequencing from Swabs/body fluids (16S) (2.5 lakh PE reads) MBS205-2L
(5 lakh PE reads) MBS205-5L
Microbiome sequencing from Soil/Sediment/Water/Fecal (16S) (2.5 lakh PE reads) MBS206-2L
(5 lakh PE reads) MBS206-5L
Microbiome sequencing from Community DNA (ITS) (2.5 lakh PE reads) MBS207-2L
(5 lakh PE reads) MBS207-5L
Microbiome sequencing from Insect/Food sample (ITS) (2.5 lakh PE reads) MBS208-2L
(5 lakh PE reads) MBS208-5L
Microbiome sequencing from Swabs/body fluids (ITS) (2.5 lakh PE reads) MBS209-2L
(5 lakh PE reads) MBS209-5L
Microbiome sequencing from Soil/Sediment/Water/Fecal (ITS) (2.5 lakh PE reads) MBS210-2L
(5 lakh PE reads) MBS210-5L
16S Microbiome ready-to-load (50,000 PE reads) MBS216
(1 lakh PE reads) MBS216-1L
(2.5 lakh PE reads) MBS216-2L
(5 lakh PE reads) MBS216-5L

 

Supplemental services

Only available in conjunction with other service codes, not independently.

Source: HiMedia Laboratories Pvt. Ltd.

Description Service Codes
DNA Fragment QC MBS304
RNA QC with RIN value MBS306

 

Transcriptomics

RNA sequencing (RNA-seq) is a potent and frequently used tool for transcriptome research, revolutionizing molecular biology. Researchers may analyze gene expression in unprecedented depth, gaining vital insights into biological processes and disease pathogenesis. RNA-seq converts RNA molecules into cDNA fragments, which are subsequently sequenced utilizing high-throughput technology.

  • Identify post-transcriptional modifications, including RNA editing
  • Identify and measure gene expression levels, locate unique transcripts, and examine alternative splicing patterns
  • Wide dynamic range and low input requirements
  • Work with a range of sample types, including single cells and complex tissues
  • Integrate with other omics data to get a more complete picture of biological systems

RNA sequencing services

Source: HiMedia Laboratories Pvt. Ltd.

Description Service Codes
de novo RNA Sequencing/Transcriptome Sequencing (10M PE reads, 2x150) MBS230-10M
de novo RNA Sequencing/Transcriptome Sequencing (20M PE reads, 2x150) MBS230-20M
de novo RNA Sequencing/Transcriptome Sequencing (30M PE reads, 2x150) MBS230-30M
Top Up Sequencing (10M PE reads, 2x150) MBS230-10MTUP
RNA Sequencing/Transcriptome Sequencing, 10Gb data(W~67M PE reads, 2x150) MBS230-10G
mRNA Sequencing/RNA Sequencing/Whole Transcriptome Sequencing (10M PE reads, 2x75) MBS231-10M
mRNA Sequencing/RNA Sequencing/Whole Transcriptome Sequencing (20M PE reads, 2x75) MBS231-20M
mRNA Sequencing/RNA Sequencing/Whole Transcriptome Sequencing (30M PE reads, 2x75) MBS231-30M

 

Custom sequencing

Sequencing and bioinformatics services with the Hi-Gx360

Image Credit: HiMedia Laboratories Pvt. Ltd.

Sequencing services

Source: HiMedia Laboratories Pvt. Ltd.

Category Description
NGS 16S Microbiome ready-to-load
NGS MiSeq ready-to-load
NGS Custom Sequencing on MiSeq
NGS NextSeq ready-to-load
NGS NextSeq ready-to-run

 


Bioinformatics services

Sequencing and bioinformatics services with the Hi-Gx360

Image Credit: HiMedia Laboratories Pvt. Ltd.

Analyzing both small and large sequence datasets from Next-Generation Sequencing (NGS) presents a significant challenge, especially with massively parallel sequencing. This is primarily due to limitations in scalable computational power and insufficient understanding of the inner workings of various bioinformatics (BioIT) tools. Furthermore, data privacy remains a daunting hurdle for researchers handling patient data.

One of the main difficulties, particularly in massively parallel sequencing, is analyzing customers’ NGS files, regardless of how big or little they are. The primary causes of issues are a lack of scalable computing capacity and an ignorance of the inner workings of various bioinformatic (BioIT) technologies.

For academics dealing with patient data, data privacy is still a formidable obstacle. Each of these issues has been methodically resolved by Hi-Gx360® at our cutting-edge bioinformatics data center. This comprises:

  • Secure datasets that are never made publicly available online
  • Open and transparent exchange of information on the analytical process
  • Analysis was performed using highly scalable and tested open-source packages
  • Secure interactive reports that are comprehensive and information-rich
  • Publication grade data visualizations
  • Direct Consultations with the highly qualified scientists on project design

With the bioinformatics services, users can accurately achieve the following:

  • Combine with short and long reads libraries to obtain complete genome sequence
  • Identify repetitive regions, structural variants and complex rearrangements for de-novo assemblies
  • Identify organisms with confidence
  • Assemble, annotate and analyze whole genomes
  • Locate low frequency mutations & identify InDels
  • Uncover genetic traits, such as antibiotic resistance markers, etc.

Bioinformatics services

BioIT services for Sanger data

Source: HiMedia Laboratories Pvt. Ltd.

Description Service Codes
Phylogenetic Analysis (16S/18S/ITS/any other gene based) MBS020
NCBI submissions MBS021
Primer Designing MBS024
Custom Analysis for Sanger Data MBS029

 

BioIT services for NGS data

Source: HiMedia Laboratories Pvt. Ltd.

Description Service Codes
Whole Genome analysis for Bacteria/ Archaea (Basic) MBS001
Whole Genome analysis for Bacteria/ Archaea (Advanced) MBS002
Whole Genome analysis for Fungi (Basic) MBS003
Whole Genome analysis for Fungi (Advanced) MBS004
Whole Genome analysis for Virus MBS005
Genome Mining for Natural Products from Bacteria/Archaea (Requires MBS001) MBS010
Genome Mining for AMR and other features from Bacteria/Archae (Requires MBS001) MBS011
Genome Based Microbial identification (Requires MBS001) MBS012
Microbiome profiling (Basic Analysis 16S/18S/ITS/any other gene based) MBS013
Microbiome profiling (Advanced Analysis 16S/18S/ITS/any other gene based) MBS014
Shotgun Metagenomics (Bacterial/ Archaeal/Viral communities) MBS015
Genome resolved Metagenomics (Bacterial/Archaeal/Viral communities) MBS016
Transcriptome analysis (Kallisto/Salmon or prokaryote) MBS017
Transcriptome analysis (HiSat/Star or eukaryote) MBS018
Whole Genome analysis for Yeast (Basic) MBS022
Whole Genome analysis for Yeast (Advanced) MBS023
SRA Submission of NGS Dataset MBS025
Whole Exome Analysis (Human) MBS027
Mitochondrial Whole Genome Analysis MBS028
Custom Analysis for NGS Data MBS026

 

Specialized in-silico genome mining services

Natural product discovery

Some of the best chemists in human history are microorganisms, which also generate a variety of bioactive chemicals. Even before beginning the expensive process of chemical characterization, genome mining can help forecast the organism's capacity for biosynthesis. The journey from discovery to manufacturing can be shortened by using the information gathered from genome mining to inform chemical synthesis.

MBS010 Genome Mining for Natural Products from Bacteria Archaea (requires MBS001)

Antimicrobial resistance profile

Antimicrobial resistance (AMR) poses a global risk to human health and development. AMR is one of the top 10 worldwide public health problems, according to WHO. Identifying control and preventative techniques is crucial for combating the growing threat of AMR. Genome mining is an effective method for accurately predicting AMR in bacteria. Hi-Gx360® offers assistance in identifying AMR indicators from an organism's genomic sequence.

MBS011 Genome Mining for AMR and other features from Bacteria/Archaea (Requires MBS001).


Products of Hi-Gx360

Hi-Gx360® library preparation kits

Whole Genome and Whole Exome Workflow.

Whole Genome and Whole Exome Workflow. Image Credit: HiMedia Laboratories Pvt. Ltd.

NGS library preparation is an important stage in sequencing operations. This approach enables researchers to examine a variety of biological topics, including genome sequencing and metagenomics, with high accuracy and efficiency. The Hi-Gx360® Library Preparation Kits can efficiently prepare libraries from many DNA sources, including human, plant, animal, and microorganisms.

Source: HiMedia Laboratories Pvt. Ltd.

Category Description Service Codes
NGS Hi-Gx360® DNA Library Preparation Kit for Illumina® Sequencing Platform MBNGS001
NGS Hi-Gx360® Targeted Capture & Enrichment of DNA Libraries MBNGS002
NGS Hi-Gx360® WES Panel MBNGS003

 

Solution

Cost per test

A single library prep kit can be used for many workflows, resulting in a cost-effective test solution.

Customers

The variety of pack sizes can help small, medium, and large-scale end users.

Sustainability

Modularly increase pack sizes to avoid kits from expiring too quickly.

Multipurpose

One core library prep kit for multiple applications.

Product benefits

Using a reproducible library preparation and target capture technique ensures reliable sequencing data for users while allowing for customization of gene panels.

DNA library profile

Consistent library profiles across sample types

 

Illumina library profile of Blood DNA.

Illumina library profile of Blood DNA. Image Credit: HiMedia Laboratories Pvt. Ltd.

Product overview

Illumina library profile of Bacterial DNA. Image Credit: HiMedia Laboratories Pvt. Ltd.

Excellent read quality in 2× 150 base chemistry

Sequencing and bioinformatics services with the Hi-Gx360

Image Credit: HiMedia Laboratories Pvt. Ltd.

Product benefits

Using a reproducible library preparation and target capture technique ensures reliable sequencing data for users while allowing for customization of gene panels.


Consumables for Sequencing

Library preparation kits

Source: HiMedia Laboratories Pvt. Ltd.

Category Description Service Codes
NGS Hi-Gx360® DNA Library Preparation Kit for Illumina® Sequencing Platform MBNGS001
NGS Hi-Gx360® Targeted Capture & Enrichment of DNA Libraries MBNGS002
NGS Hi-Gx360® WES Panel MBNGS003

 

Extraction kits

Source: HiMedia Laboratories Pvt. Ltd.

Product Name Product Code
HiPurA® Blood Genomic DNA Miniprep Purification Kit MB504
HiPurA® Bacterial Genomic DNA Purification Kit MB505
HiPurA® Soil DNA Purification Kit MB542
HiPurA® HP Fungal DNA Purification Kit
(following bead beating method)
MB576
HiPurA® Pre-filled Cartridges for Bacterial DNA Purification MB505PC16-48PR
HiPurA® Pre-filled Plates for Bacterial DNA Purification MB505MPF16-96PR
HiPurA® Pre-filled Cartridges for Fungal DNA Extraction MB576PC16-48PR
HiPurA® Pre-filled Plates for Fungal DNA Extraction MB576MPF16-96PR

 

Reagents

Source: HiMedia Laboratories Pvt. Ltd.

Product Name Product Code
1kb DNA Ladder MBT051
50bp DNA Ladder MBT084
100bp DNA Ladder MBT049
6X Gel Loading Buffer ML015
2X PCR TaqMixture MBT061
2-Propanol MB063
Poly(ethylene glycol) MW 8000 MB150
1N Sodium hydroxide ML195
5M Sodium chloride ML008
1M Tris-Cl, pH 8.5 ML152
3M Sodium acetate, pH 5.2-5.4 ML009
0.5M EDTA, pH 8.0 ML014
Molecular Biology Grade Water for PCR ML065
RNase Kil™ ML162
1X PBS Solution ML116
Agarose, Ultrapure, Low EEO MB229
HiPurA® Mag Beads for Cleanup ML239
DNA Kil™ ML221

 

Lab Consumables

Source: HiMedia Laboratories Pvt. Ltd.

Product Name Product Code
PCR Blocks (Full-skirt, natural, sterile, DNA/RNAse free 96 well, 0.1ml) PR2
PCR Blocks (Semi-skirt, natural, sterile, DNA/RNAse free 96 well, 0.2 ml volume) PR3
PCR Blocks (Non-skirt, natural, sterile, RNase, DNase free, 96 well, 0.2 ml volume) PR19
Aluminium Sealing Film PR20
Optical Sealing Film 96 well PCR plate PR18
96 Well Plate for Sequencing/PCR PR26
Silicone Mat for 96- well plates (PCR) PR27
8 strip PCR tubes with optically clear attached flat caps for Real-time PCR PR23
PCR Tubes, Flat lid Autoclavable, Conical Bottom, with Graduation CG281
PCR Tubes, Thin walled DNase/RNase free,
Autoclavable, Conical Bottom, without Graduation, Flat lid
PW1255
Micro Centrifuge Tube - B PW146
HiPer® Lock MicroCentrifuge Tube, 2.0 ml MBLA017
Barrier Tips, 10 μl LA749A
Barrier Tips XL, Max. capacity 10 μl LA749XL
Barrier Tips, 20 µl LA750A
Barrier Tips XL, Max Capacity 20 µl LA750XL
Barrier Tips, 100 μl LA1104A
Barrier Tips, 200 µl LA751A
Barrier Tips, 1000 μl LA859A
Polypropylene Cryogenic Storage Box PW1215

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