Health / Pharmaceuticals
1,449 RESULTS WITHIN anywhere FROM https:, India
630, Vivek Vihar New Sanganer Road Jaipur- 302019 Rajasthan, India, Jaipur
Tel: 141-2212677
The regime of Ayurveda is centuries old and there is no doubt in the fact that it is still ruling the world with its beneficial aids. Hishimo Pharmaceuticals Pvt. Ltd. is the highly demanding Herbal Supplement Manufacturers in the national as well as the international market areas for offering a wide range of the herbal medicines for some common and some rare disorders. Since 1982 we are known for developing and delivering quality conscious safe solutions to replace the drugs and keep you fit and fine no matter how serious the problems are. From heart to liver we have all... read more
Tel: 141-2212677
The regime of Ayurveda is centuries old and there is no doubt in the fact that it is still ruling the world with its beneficial aids. Hishimo Pharmaceuticals Pvt. Ltd. is the highly demanding Herbal Supplement Manufacturers in the national as well as the international market areas for offering a wide range of the herbal medicines for some common and some rare disorders. Since 1982 we are known for developing and delivering quality conscious safe solutions to replace the drugs and keep you fit and fine no matter how serious the problems are. From heart to liver we have all... read more
45-1 Ramsey Road, Shirley, New York 11967, USA, Shirley
Profacgen makes use of state-of-the-art docking software tools to find the relative transformation and conformation of the protein and nucleic acid involved in energetically favorable complex formation. The general procedures are: First a rigid body global search is performed and geometrically plausible protein–nucleic acid complex structures are generated.... read more
Profacgen makes use of state-of-the-art docking software tools to find the relative transformation and conformation of the protein and nucleic acid involved in energetically favorable complex formation. The general procedures are: First a rigid body global search is performed and geometrically plausible protein–nucleic acid complex structures are generated.... read more
45-1 Ramsey Road, Shirley, New York 1196, Shirley
At Profacgen we use lentiviral vector for efficient gene delivery and to achieve high integration rate. Limited dilution and antibiotics screening are then applied to select for high-yield genetically homogenous stable expression monoclones. When fluorescent protein is fused to the target protein we can also use flow cytometry to screen for positive clones. Profacgen also offers the generation of Tet-ON inducible stable cell lines for inducible expression of your target gene. Doxycycline can then be used to induce the expression of your target gene.... read more
At Profacgen we use lentiviral vector for efficient gene delivery and to achieve high integration rate. Limited dilution and antibiotics screening are then applied to select for high-yield genetically homogenous stable expression monoclones. When fluorescent protein is fused to the target protein we can also use flow cytometry to screen for positive clones. Profacgen also offers the generation of Tet-ON inducible stable cell lines for inducible expression of your target gene. Doxycycline can then be used to induce the expression of your target gene.... read more
45-1 Ramsey Road, Shirley, New York 11967, USA, Shirley
Profacgen has organized a team of scientists with extensive experience in the study of PPIs to offer you one-stop service on your PPI project. We can help with your experiment design carry out your experiments and perform data analysis. We have established in our lab a series of assays to help with your research including high throughput interaction screening assays such as Yeast two-hybrid screening and phage display technology interaction strength and kinetics assays such as Surface Plasmon Resonance (SPR). Each approach has its own advantages and weaknesses in terms of sensitivity and specificity. While you can choose the techniques... read more
Profacgen has organized a team of scientists with extensive experience in the study of PPIs to offer you one-stop service on your PPI project. We can help with your experiment design carry out your experiments and perform data analysis. We have established in our lab a series of assays to help with your research including high throughput interaction screening assays such as Yeast two-hybrid screening and phage display technology interaction strength and kinetics assays such as Surface Plasmon Resonance (SPR). Each approach has its own advantages and weaknesses in terms of sensitivity and specificity. While you can choose the techniques... read more
45-1 Ramsey Road, Shirley, New York 11967, USA, Shirley
Profacgen takes advantage of the most state-of-the-art VS techniques and software tools for hit and lead identification. The application of VS follows a typical sequence of processes with a cascade of sequential filters able to narrow down and choose a set of lead-like hits with potential biological activity. We offer both ligand-based virtual screening (LBVS) and structure-based virtual screening (SBVS) services.... read more
Profacgen takes advantage of the most state-of-the-art VS techniques and software tools for hit and lead identification. The application of VS follows a typical sequence of processes with a cascade of sequential filters able to narrow down and choose a set of lead-like hits with potential biological activity. We offer both ligand-based virtual screening (LBVS) and structure-based virtual screening (SBVS) services.... read more
45-1 Ramsey Road, Shirley, New York 11967, USA, Shirley
The electrophoretic mobility shift assay (EMSA) or gel shift assay is a simple and rapid method to detect protein complexes with nucleic acids. EMSA originally used widely in the study of sequence-specific DNA-binding proteins such as transcription factors has been further developed to investigate DNA-protein interactions RNA-protein interactions and even DNA-RNA interactions. It is also applied to qualify and quantify proteins that specifically bind to given nucleotides enabling to accommodate a wide range of binding conditions.... read more
The electrophoretic mobility shift assay (EMSA) or gel shift assay is a simple and rapid method to detect protein complexes with nucleic acids. EMSA originally used widely in the study of sequence-specific DNA-binding proteins such as transcription factors has been further developed to investigate DNA-protein interactions RNA-protein interactions and even DNA-RNA interactions. It is also applied to qualify and quantify proteins that specifically bind to given nucleotides enabling to accommodate a wide range of binding conditions.... read more
45-1 Ramsey Road, Shirley, New York 11967, USA, Shirley
Pioneered by Stanley Fields and Ok-Kyu Song in 1989 the yeast-two-hybrid (Y2H) technique was originally designed to detect protein–protein interactions using the GAL4 transcriptional activator of the yeast Saccharomyces cerevisiae. Nowadays the Y2H screen remains one of the leading molecular tools to study protein-protein interactions in native intracellular conditions. This screen is not only cheap and easy to operate but can also be carried out in almost any laboratory with results seen within a matter of days. In addition compared to other methods used to study protein-protein interactions such as crosslinking and coimmunoprecipitation the Y2H screen allows detecting weak and... read more
Pioneered by Stanley Fields and Ok-Kyu Song in 1989 the yeast-two-hybrid (Y2H) technique was originally designed to detect protein–protein interactions using the GAL4 transcriptional activator of the yeast Saccharomyces cerevisiae. Nowadays the Y2H screen remains one of the leading molecular tools to study protein-protein interactions in native intracellular conditions. This screen is not only cheap and easy to operate but can also be carried out in almost any laboratory with results seen within a matter of days. In addition compared to other methods used to study protein-protein interactions such as crosslinking and coimmunoprecipitation the Y2H screen allows detecting weak and... read more
45-1 Ramsey Road, Shirley, New York 11967, USA, Shirley
Surface plasmon resonance (SPR) is one of the commonly used technologies for detailed and quantitative studies of protein-protein interactions and determination of their equilibrium and kinetic parameters. SPR provides excellent instrumentation for a label-free real-time investigation of protein-protein interactions.... read more
Surface plasmon resonance (SPR) is one of the commonly used technologies for detailed and quantitative studies of protein-protein interactions and determination of their equilibrium and kinetic parameters. SPR provides excellent instrumentation for a label-free real-time investigation of protein-protein interactions.... read more
45-1 Ramsey Road, Shirley, New York 11967, USA, Shirley
Co-Immunoprecipitation (Co-IP) was developed from the immunoprecipitation technique with which Co-IP shares the fundamental principle of the specific antigen-antibody reaction. Immunoprecipitation(IP) technique is used for isolate individual protein. Using an antibody that is specific for a particular protein the target protein could be isolated out from a crude lysate of a plant or animal tissue or other biological regent.... read more
Co-Immunoprecipitation (Co-IP) was developed from the immunoprecipitation technique with which Co-IP shares the fundamental principle of the specific antigen-antibody reaction. Immunoprecipitation(IP) technique is used for isolate individual protein. Using an antibody that is specific for a particular protein the target protein could be isolated out from a crude lysate of a plant or animal tissue or other biological regent.... read more
45-1 Ramsey Road, Shirley, NY 11967, USA, Shirley
Tel: 1-631-275-3058
Absolute Quantification is a targeted quantitative proteomics technique that exhibits robust efficacy and is being increasingly utilized for a wide variety of quantitative proteomics studies. AQUA strategy is for the absolute quantification (AQUA) of proteins and their modification states. Peptides are synthesized with incorporated stable isotopes as ideal internal standards to mimic native peptides formed by proteolysis. These synthetic peptides can also be prepared with covalent modifications (e. g. phosphorylation methylation acetylation etc.) that are chemically identical to naturally occurring posttranslational modifications. Such AQUA internal standard peptides are then used to precisely and quantitatively measure the absolute levels of proteins... read more
Tel: 1-631-275-3058
Absolute Quantification is a targeted quantitative proteomics technique that exhibits robust efficacy and is being increasingly utilized for a wide variety of quantitative proteomics studies. AQUA strategy is for the absolute quantification (AQUA) of proteins and their modification states. Peptides are synthesized with incorporated stable isotopes as ideal internal standards to mimic native peptides formed by proteolysis. These synthetic peptides can also be prepared with covalent modifications (e. g. phosphorylation methylation acetylation etc.) that are chemically identical to naturally occurring posttranslational modifications. Such AQUA internal standard peptides are then used to precisely and quantitatively measure the absolute levels of proteins... read more
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