Genetic Testing

DNA Predisposition Genetic Test It is the test that analyze persons genetic variants to identify Inherited risk for the disease and health conditions. It does not diagnose disease but reveals the likelihood of developing metabolism ,Cardiovascular, Renal, Neurological, and lifestyle related risk Technology used in this test- A high-throughput platform that examines thousands of genetic markers (SNPs) at once. Approximately 750,000 genetic markers It maps the patient s genetic variations linked to disease risk, metabolism, and biological functions

Biological samples will be collected for genetic testing and based on the test price will be fixed. All services will be done in Bangalore pvt lab. Doctor prescription needed for all test services.

The QIAGEN Type-it HRM PCR Kit is designed for high-resolution melting (HRM) analysis, enabling precise mutation scanning and genotyping. It uses a novel EvaGreen dye for improved melting curve discrimination and is optimized for use on various real-time PCR instruments. The kit contains a ready-to-use master mix with HotStarTaq Plus DNA Polymerase and Q-Solution, ensuring robust performance and minimal optimization. Note The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263Key Features High Sensitivity Specificity Ready-to-Use Master Mix Broad Instrument Compatibility No Optimization Required Disclaimer - UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R Refurbished, PO Preowned, U Used, T Trading, M Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer

QIAGEN dPCR CNV Probe Assays are hydrolysis probe-based digital PCR assays developed for copy number variation (CNV) analysis of specific genes or genomic regions using the QIAcuity Digital PCR System. These assays provide precise, sensitive, and reproducible CNV detection, making them ideal for applications in genetic research, cancer biology, and pharmacogenomics. Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860. Key Features: Wide Assay Coverage: Over 200 wet-lab validated assays targeting human genes Includes gene of interest (GOI) assays, centromeric reference assays, and single-copy references Flexible Multiplexing: Detect up to 5 targets per reaction Available in a variety of fluorophores: FAM , HEX , Atto 550, ROX , Cy5 Minimal Sample Input: Sensitive enough to detect single-copy changes with low DNA input (as little as 4 6 ng per reaction) Robust Across Sample Types: Validated for FFPE, fresh/frozen tissues, cell lines, and inhibited samples Fast and Easy Workflow: Complete CNV analysis within ~2 hours Seamless integration with the QIAcuity Software Suite for automatic CNV calculations High Precision and Reproducibility: Reliable copy number calls with minimal need for replicates Industries Served: Genetic Research Genomics Cancer Biology Oncology Pharmacogenomics Clinical Research Biopharmaceutical Development Molecular Diagnostics (RUO settings) Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R Refurbished, PO Preowned, U Used, T Trading, M Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer. ( Final Price will be given by Sales team )

Genetic testing using RTPCR, PCR, sequencing, DNA, RNA isolation, cloning, expression studies, agarose gel, SDS page, western blotting

This unique kit contains simple activities designed to teach basic fruit fly genetics without using live flies. Drosophila Melanogaster is used without the inconvenience of maintaining live fruit fly cultures. Includes 15 sheets each, with snap apart features showing male and female and 4 types of fruit flies. Students can perform crosses using plastic pieces printed with features allowing them to observe and simulate sex determination, single factor inheritance, double factor inheritance, sex linkage, dominance and recessiveness. Teacher's Guide and Student instruction sheet included.

If you suffer from clinical symptoms of unknown reason or have a positive family history of any suspected hereditary disease, genomic testing can provide answers and make a precise diagnosis, in order to find certainty and start timely treatment. With myLifeDNA , we sequence your entire genomic DNA and interpret selected genes based on your clinical symptoms as well as personal and family medical history. After every analysis, you will receive a detailed report with further information and action points. myLifeDNA also includes a subscription to quarterly updates of your results based on most recent scientific knowledge. Highest-quality interpretation of your genomic data Analysis of genes based on specific symptoms and positive family history Includes a pool of more than 20,000 genes Quarterly updated results based on scientific knowledge Access to professional genomic counseling SamplingKit and global free shipping included Why genomic testing? More than 500 million people globally are suffering from a genomic disorder. An early diagnosis is critical to bring the most benefit to the quality of life and the overall prognosis of these patients. The difficulty with the large variety of different genomic disorders is that they have overlapping and atypical symptoms. Finding the correct diagnosis is extremely difficult. Only a genomic test can unravel relevant mutations, also called pathogenic variants, and identify the cause of a disease. The human genome has a length of approximately 3.2 billion nucleotides, i.e. letters. But where would you look when you don t know which part of your genome could be the cause of your symptoms? The most practicable solution: You directly check the entire genomic information in your cells, is what we call whole genome . Whole Genome Sequencing (WGS) is the most modern solution to get our entire genomic information decoded. Arcensus calls its genomic testing exclusively genomic because we are one of the few companies globally that is offering solely the medical Whole Genome Sequencing directly to consumers. While the first deciphering of the human genome costed $3 billion, the costs are steadily decreasing due to progressing technologies. Today, we have reached a point where a WGS analysis is becoming affordable. With myLifeDNA , Arcensus offers the ideal package for all people that have: Clinical symptoms of unknown reason A high degree suspicion of a genomic disease A positive family history for any genetically suspected problem The wish just to get their genome analysed to have the best preventive data information The strength in Arcensus approach is the combination of both the Whole Genome Sequencing analysis and the integration of the person s clinical symptoms together with a life-long partnership. Only WGS analysis can bring you the reliability to reduce the risk of missing any potential pathogenic variant in your genome to the barest minimum Based on the description of your clinical symptoms and family history, our medical and genomic experts are able to get a deep understanding of your genome data and to narrow down the analysis of your whole genome data to relevant genes for your condition Only in the combination of the Whole Genome Sequencing, medical report, a quarterly updated report, and the newest scientific findings you will receive the best level of medical and scientific precision

Mutagenicity refers to the permanent transmissible variations in the amount and structure of genetic materials of cells or organisms that can increase the frequency of mutations Method: In vitro genotoxicity tests assess mutation and chromosomal damage by exposing cells to chemicals or agents and examining genetic material damage indicators. These may include chromosomal structure or number alterations, DNA mutations, or other genetic changes. Claims: Non Genotoxic, Non Carcinogenic Turn Around Time: 4-6 weeks.

SLS Research offers a comprehensive set of real time PCR services (also referred to as quantitative PCR services or qPCR services), including gene expression, miRNA expression, SNP genotyping, copy number variation, and absolute quantification. Gene expression analysis is most simply described as the study of the way genes are transcribed to synthesize functional gene products functional RNA species or protein products. The study of gene regulation provides insights into normal cellular processes, such as differentiation, and abnormal or pathological processes. Our real-time PCR (qPCR) services begin with a design consultation to understand your qPCR application, desired chemistry (TaqMan or SYBR Green), and desired data output. Our experienced application scientists will help you settle on a real-time PCR (qPCR) services workflow that fits your needs and budget.

The QIAgility is a compact benchtop instrument that enables rapid, high-precision setup of PCR experiments with ready-to-use software for ease and convenience. The software provides step-by-step guidance for worktable setup and automatic calculation of all mixes, eliminating the need to program pipetting steps. Just select the kit and cycler, define your targets and start the run. For added flexibility the QIAgility is operated via a laptop computer.

The Applied Biosystems SeqStudio Genetic Analyzer is a low-throughput, easy-to-use, and convenient benchtop system that delivers gold-standard Sanger sequencing technology and fragment analysis by capillary electrophoresis with a simple click. Just load your samples, click in the innovative all-in-one cartridge, and go. The SeqStudio instrument is easy to use across a broad range of applications, including de novo, targeted, and plasmid Sanger sequencing, CRISPR-Cas9 genome editing confirmation, cell line authentication, and detection of single nucleotide polymorphisms (SNPs). Setup is simple and you will be ready to go in minutes. The SeqStudio Genetic Analyzer offers data quality, usability, service, and support at an affordable price.

The Applied Biosystems SeqStudio Genetic Analyzer is a low-throughput, easy-to-use, and convenient benchtop system that delivers gold-standard Sanger sequencing technology and fragment analysis by capillary electrophoresis with a simple click. Just load your samples, click in the innovative all-in-one cartridge, and go. The SeqStudio instrument is easy to use across a broad range of applications, including de novo, targeted, and plasmid Sanger sequencing, CRISPR-Cas9 genome editing confirmation, cell line authentication, and detection of single nucleotide polymorphisms (SNPs). Setup is simple and you will be ready to go in minutes. The SeqStudio Genetic Analyzer offers data quality, usability, service, and support at an affordable price.

Genetic Counselling is the process of helping people understand and adapt to the medical, psychological and familial implications of genetic contributions to disease. This process integrates: Interpretation of family and medical histories to assess the chance of disease occurrence or recurrence. Education about inheritance, testing, management, prevention, resources Counselling to promote informed choices and adaptation to the risk or condition. Reasons for testing:Detectable conditionsAdult geneticsART/Infertility geneticsCardiovascular geneticsHereditary cancerPeadiatric cancerNeurogeneticsPrenatal geneticsPsychiatric geneticsMetabolismPreventive healthcare

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For direct manufacturers/end users only Not for Resale. The SeqStudio Genetic Analyzer offers users the flexibility to set up their plate and samples, and start a run. Additional run modules can be created or modified via the integrated and interactive touchscreen. Results can be viewed in various formats on the screen, including a list or in plate view as well as from the sequencing plots or raw electropherograms. A comprehensive Applied Biosystems software package includes the following: Sequencing Analysis Software uses a base-caller algorithm for pure- and mixed-base calls; analyzes, displays, edits, saves, and prints sample files generated from Applied Biosystems DNA and genetic analyzers SeqScape Software designed for mutation detection and analysis, SNP discovery, pathogen subtyping, allele identification, and sequence confirmation Variant Reporter Software designed for referencebased and non-reference based analysis such as mutation detection and analysis, SNP discovery, and sequence confirmation GeneMapper Software designed to provide DNA sizing and quality allele calls for all Applied Biosystems electrophoresis-based genotyping systems; specializes in multiapplication functionality, including amplified fragment length polymorphism (AFLP) analysis, loss of heterozygosity (LOH), and microsatellite and SNP genotyping analysis; includes security and audit features MVF Software enables 5% somatic variant detection using Sanger sequencing, making Sanger sequencing a fast, cost-effective, and accurate way to call low-frequency somatic variants where the number of relevant targets is limited

Genetic counseling services are now gaining popularity in India and are available at some 40 or so centres spread across the countryThis process integrates interpretation of family and medical histories to assess the chance of disease occurrence or recurrenceEducation about inheritance, testing, management, prevention, resources.

CGT is an advanced carrier genetic test before pregnancy, which determines whether a couple is a carrier of genetic mutations that could be transmitted to their children.It analyses more than 6,600 mutations associated with over 600 genetic disorders such as Beta Thalassemia, Spinal Muscular Atrophy, Sickle Cell, Hemophilia A, DMD, Fragile X among others by NGS.BenefitsStudy on more than 6,600 mutations associated with over 600 genetic disorders.Genetic counseling for patients and specialists.Genetic screening test based on Next Generation Sequencing (NGS) and clinically validated. Indications For any Couples under a consanguineous marriage before planning to conceive naturally or through an assisted reproduction treatment.For Couples with an affected child or family history of disorder.For Couples who wants to form a family to know the risk of transmitting hereditary disorders to their children.Before a treatment with donor sperm or eggs.Most carriers of genetic mutations don t have a family history of these disorders.

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Even though most children are born healthy, there are many children born with medical complications. Many of these birth defects are due to genetics. These birth defects results in diseases such as Down syndrome, sickle cell anaemia, Cystic fibrosis, congenital heart disease, Williams syndrome etc.Genetic testing in paediatric patients is used in the investigation of a range of clinical concerns. These may be systemic syndromes, developmental delay, mental retardation, autistic spectrum disorders, neurodevelopmental disorders, short stature or delayed puberty, in-born errors of metabolism, multifactorial disorders, or they may be more specific, such as in diagnosis of suspected cystic fibrosis. In neonatology genetic testing is often used for the investigation of dysmorphic features, hypotonia, ambiguous genitalia, metabolic and systemic syndromes and other clinical conditions associated with genetic causes.We diagnose various genetic disorders in children and our expert team will also give guidance for parents in dealing with genetic disorders in children.

Specification:Karyotyping systemFish SystemHi KSYCHG Comet assay Kreatech Probes ? Prenatal, BCR ABL, AML etc.

Sandor Lifesciences is a DSIR recognized and NABL accredited laboratory in the country to offer services in biochemical genetics. Established with the training of our staff in different foreign laboratories like Erasmus Medical Centre, Amsterdam Medical centre and Shimani University, our laboratories offer services in New born screening, diagnosis for Inherited Metabolic Disorders such as organic acidurias, amino acidopathies, lysosomal storage disorders, Molecular Genetics, Cytogenetics, diagnosis etc.

Genetic testing on preventive diseases usually occurs after age 40. Possible early diagnosis of diseasesPrevention of diseasesAdvice on medication based on your genes.

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Genetics is the science identifying the genes & their abnormalities. This is done by chromosomal cultures & identification of locations of various genes. This procedure of Karyotyping is done on very high-end instruments at S.N. Gene. Lab. Dr. Vaidya s Laboratory has technical association with S N gene lab. Many tests of Karyotyping, special tests like FISH & PCR for diseases like HIV, Tuberculosis are done in short time. It is possible to give final diagnosis of these diseases. Allergy is a problem which can be prevented better than cure. Dr Vaidya s Laboratory has special tests like Allergy screen on machine called Rida Screen. This can identify comman allergens as well as food & respiratory antigens. Special pediatric panel is also available. Laboratory has high-end instrument like Centaur XP, Immulite & Mini-Vidas for many special immunoassays. These includes hormones for thyroid, sterility & IVF panels. We also perform assays like Vit. D, Vit B12 etc. Various cancer marker & tests like D-dimmer, fibrinogens, Lupus anticoagulant are possible. Our serology department can perform many special tests like Dengue Antigen & antibodies, Leptospira, AMH in addition to infections screen.

High-Throughput Capability: Designed for efficient processing of multiple samples, allowing researchers to obtain results quickly and accurately.Integrated Software: Comes with intuitive software for data analysis, making it easy to interpret sequencing results and generate reports.Versatile Applications: Suitable for various genetic analyses, including SNP genotyping, sequencing, and fragment analysis, making it ideal for both clinical and research laboratories.Compact Design: Its space-saving design allows for easy integration into existing lab setups, maximizing productivity without compromising on performance.

Genetic testing, also known as DNA testing, allows the determination of bloodlines and the genetic diagnosis of vulnerabilities to inherited diseases. In agriculture, a form of genetic testing known as progeny testing can be used to evaluate the quality of breeding stock. In population ecology, genetic testing can be used to track genetic strengths and vulnerabilities of species populations.In humans, genetic testing can be used to determine a child's parentage (genetic mother and father) or in general a person's ancestry or biological relationship between people. In addition to studying chromosomes to the level of individual genes, genetic testing in a broader sense includes biochemical tests for the possible presence of genetic diseases, or mutant forms of genes associated with increased risk of developing genetic disorders.Genetic testing identifies changes in chromosomes, genes, or proteins. The variety of genetic tests has expanded throughout the years. In the past, the main genetic tests searched for abnormal chromosome numbers and mutations that lead to rare, inherited disorders. Today, tests involve analyzing multiple genes to determine the risk of developing specific diseases or disorders, with the more common diseases consisting of heart disease and cancer. The results of a genetic test can confirm or rule out a suspected genetic condition or help determine a person's chance of developing or passing on a genetic disorder. Several hundred genetic tests are currently in use, and more are being developed.

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