Protein Analysis
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Distance: 12,798.63km
45-1 Ramsey Road, Shirley, NY 11967, USA, shirley
Glycosylation the attachment of sugar moieties to proteins is a post-translational modification (PTM) that provides greater proteomic diversity than other PTMs. Glycosylation is critical for a wide range of biological processes including cell attachment to the extracellular matrix and protein-ligand interactions in the cell. This PTM is characterized by various glycosidic linkages including N- O- and C-linked glycosylation glypiation (GPI anchor attachment) and phosphoglycosylation. Glycoproteins can be detected purified and analyzed by different strategies including glycan staining and visualization glycan cross-linking to agarose or magnetic resin for labeling or purification or proteomic analysis by mass spectrometry respectively.... read more
Glycosylation the attachment of sugar moieties to proteins is a post-translational modification (PTM) that provides greater proteomic diversity than other PTMs. Glycosylation is critical for a wide range of biological processes including cell attachment to the extracellular matrix and protein-ligand interactions in the cell. This PTM is characterized by various glycosidic linkages including N- O- and C-linked glycosylation glypiation (GPI anchor attachment) and phosphoglycosylation. Glycoproteins can be detected purified and analyzed by different strategies including glycan staining and visualization glycan cross-linking to agarose or magnetic resin for labeling or purification or proteomic analysis by mass spectrometry respectively.... read more
Distance: 12,798.63km
45-1 Ramsey Road, Shirley, New York 11967, USA, Shirley
Protein-protein interactions (PPIs) are established when protein molecules physically contact with each other through hydrogen or hydrophobic bonds Van der Waals forces ionic forces or even covalent bonds. This phenomenon underlies a wide range of essential cellular events such as signal transduction molecular transport and various metabolism pathways. PPIs are also the basic of many diseases. Therefore PPIs have been studied extensively in the area of bioscience and medical research. 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... read more
Protein-protein interactions (PPIs) are established when protein molecules physically contact with each other through hydrogen or hydrophobic bonds Van der Waals forces ionic forces or even covalent bonds. This phenomenon underlies a wide range of essential cellular events such as signal transduction molecular transport and various metabolism pathways. PPIs are also the basic of many diseases. Therefore PPIs have been studied extensively in the area of bioscience and medical research. 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... read more
Distance: 12,798.63km
45-1 Ramsey Road, Shirley, NY 11967, USA, shirley
Tel: 6316269181
Structure determination is usually a tedious and expensive process whereby the target macromolecule must be produced in relatively large quantities and purified in high concentrations. A successful experiment often requires expert knowledge of biochemistry bioinformatics and molecular biology. Over the past decades rapid technical advances in DNA cloning protein expression and purification methodologies have made it generally easy to obtain enough amount of proteins for their structural study. Besides numerous innovations and improvements have been made in solving protein structures using instrumental methods such as X-ray crystallography nuclear magnetic resonance (NMR) spectroscopy and electron microscopy (EM). These efforts together have... read more
Tel: 6316269181
Structure determination is usually a tedious and expensive process whereby the target macromolecule must be produced in relatively large quantities and purified in high concentrations. A successful experiment often requires expert knowledge of biochemistry bioinformatics and molecular biology. Over the past decades rapid technical advances in DNA cloning protein expression and purification methodologies have made it generally easy to obtain enough amount of proteins for their structural study. Besides numerous innovations and improvements have been made in solving protein structures using instrumental methods such as X-ray crystallography nuclear magnetic resonance (NMR) spectroscopy and electron microscopy (EM). These efforts together have... read more
Distance: 12,798.63km
45-1 Ramsey Road, Shirley, New York 11967, USA, Shirley
CLIP (cross-linking immunoprecipitation) is a method used to analyze RNA-protein interactions or locate precise RNA modifications. This technique is performed by immunoprecipitation with an antibody against the protein-of-interest after UV cross-linking of the RNA-protein complex. CLIP-Seq which is also known as HITS-CLIP combines CLIP with high-throughput sequencing for identification of binding sites on RBPs. CLIP-Seq can be used to map RNA-binding landscape of interacting proteins or RNA modification sites on a genome-wide scale which helps facilitate the understanding towards post-transcriptional regulatory networks and mechanisms.... read more
CLIP (cross-linking immunoprecipitation) is a method used to analyze RNA-protein interactions or locate precise RNA modifications. This technique is performed by immunoprecipitation with an antibody against the protein-of-interest after UV cross-linking of the RNA-protein complex. CLIP-Seq which is also known as HITS-CLIP combines CLIP with high-throughput sequencing for identification of binding sites on RBPs. CLIP-Seq can be used to map RNA-binding landscape of interacting proteins or RNA modification sites on a genome-wide scale which helps facilitate the understanding towards post-transcriptional regulatory networks and mechanisms.... read more
Distance: 12,798.63km
155 Federal Street, Boston
In the life of an organism the function of proteins is achieved by the interaction between proteins and proteins. Therefore the study of new proteins can provide new directions for the study of the potential function of proteins. In many protein tests pull-down assays are often used to test protein-protein-interaction. Pull-down's experiment uses highly purified and enriched bait protein to capture the targeted proteins that specifically interact with the bait protein in the cell and greatly improve the efficiency of identification of new target protein. The specific steps of pull-down's experiment are to express the bait protein modified with poly-His... read more
In the life of an organism the function of proteins is achieved by the interaction between proteins and proteins. Therefore the study of new proteins can provide new directions for the study of the potential function of proteins. In many protein tests pull-down assays are often used to test protein-protein-interaction. Pull-down's experiment uses highly purified and enriched bait protein to capture the targeted proteins that specifically interact with the bait protein in the cell and greatly improve the efficiency of identification of new target protein. The specific steps of pull-down's experiment are to express the bait protein modified with poly-His... read more
Distance: 12,798.63km
155 Federal Street, Suite 700, Boston
Isobaric Tag for Relative Absolute Quantitation (iTRAQ) and Tandem Mass Tags (TMT) are two similar quantitative proteomic techniques developed by AB SCIEX and Thermo Fisher respectively. The most distinctive advantage of these two techniques is that they can label up to 10 different samples and compare the relative proteomic change through LC-MS/MS analysis. Therefore these techniques are widely applied to study proteomic changes under different treatments or in different development stages. MtoZ Biolabs is proud to offer iTRAQ/TMT analysis service to meet your research needs. On the basis of these two well-established techniques we can also provide MultiNotch MS analysis... read more
Isobaric Tag for Relative Absolute Quantitation (iTRAQ) and Tandem Mass Tags (TMT) are two similar quantitative proteomic techniques developed by AB SCIEX and Thermo Fisher respectively. The most distinctive advantage of these two techniques is that they can label up to 10 different samples and compare the relative proteomic change through LC-MS/MS analysis. Therefore these techniques are widely applied to study proteomic changes under different treatments or in different development stages. MtoZ Biolabs is proud to offer iTRAQ/TMT analysis service to meet your research needs. On the basis of these two well-established techniques we can also provide MultiNotch MS analysis... read more
Distance: 12,798.63km
155 Federal Street, Suite 700, Boston
Similar to SILAC technique Dimethyl labeling is also an isotopic labeling method. However Dimethyl labeling is a chemical labeling process and labels lysine or the N-terminal amino acid residues on peptide instead of labeling proteins. Except for the difference in labeling method SILAC and Dimethyl labeling technique have comparable sensitivity and accuracy and are being more and more widely used in relative proteomics studies. MtoZ Biolabs has developed a specialized platform equipped with Q Exactive HF (Thermo Fisher) Orbitrap Fusion and Orbitrap Fusion Lumos mass spectrometers equipped with Nano-LC for SILAC/Dimethyl analysis service.... read more
Similar to SILAC technique Dimethyl labeling is also an isotopic labeling method. However Dimethyl labeling is a chemical labeling process and labels lysine or the N-terminal amino acid residues on peptide instead of labeling proteins. Except for the difference in labeling method SILAC and Dimethyl labeling technique have comparable sensitivity and accuracy and are being more and more widely used in relative proteomics studies. MtoZ Biolabs has developed a specialized platform equipped with Q Exactive HF (Thermo Fisher) Orbitrap Fusion and Orbitrap Fusion Lumos mass spectrometers equipped with Nano-LC for SILAC/Dimethyl analysis service.... read more
Distance: 12,798.63km
155 Federal Street, Suite 700, Boston
Sequential Window Acquisition of all Theoretical fragment ions (SWATH) is a brand new mass spectrometry technology co-developed by Dr. Ruedi Aebersold research group (ETH Zürich) and AB SCIEX. SWATH data is an independent acquisition (DIA) technique. Unlike data dependent acquisition technique which only selects certain MS spectrum for MS/MS detection SWATH analyzes all MS and MS/MS spectra allowing detection of virtually all detectable proteins in a sample. In SWATH technology MS spectra are divided into several narrow windows and peptides in each window are sequentially analyzed equally followed by MS/MS analysis. SWATH technique combines the high-throughput quality of shotgun proteomics... read more
Sequential Window Acquisition of all Theoretical fragment ions (SWATH) is a brand new mass spectrometry technology co-developed by Dr. Ruedi Aebersold research group (ETH Zürich) and AB SCIEX. SWATH data is an independent acquisition (DIA) technique. Unlike data dependent acquisition technique which only selects certain MS spectrum for MS/MS detection SWATH analyzes all MS and MS/MS spectra allowing detection of virtually all detectable proteins in a sample. In SWATH technology MS spectra are divided into several narrow windows and peptides in each window are sequentially analyzed equally followed by MS/MS analysis. SWATH technique combines the high-throughput quality of shotgun proteomics... read more
Distance: 12,798.63km
155 Federal Street, Suite 700, Boston
Bioamine is a kind of low molecular weight compounds containing nitric fatty group or heterocycle group. Depending on the composition of amine bioamine can be divided into two classes monoamine and polyamine. Monoamine plays a role in muscular and blood vessel relaxation and regulates cerebral cortex activity. Polyamine mainly promotes synthesis of macromolecules including DNA RNA and proteins and accelerates development and growth. MtoZ Biolabs offers targeted bioamine analysis service using ACQUITY UPLC/TripleQuad5500 (Waters/AB Sciex) which have characteristics of high accuracy specificity and sensitivity. We guarantee accurate analysis of bioamine even in low abundance. With our optimized sample preparation methods... read more
Bioamine is a kind of low molecular weight compounds containing nitric fatty group or heterocycle group. Depending on the composition of amine bioamine can be divided into two classes monoamine and polyamine. Monoamine plays a role in muscular and blood vessel relaxation and regulates cerebral cortex activity. Polyamine mainly promotes synthesis of macromolecules including DNA RNA and proteins and accelerates development and growth. MtoZ Biolabs offers targeted bioamine analysis service using ACQUITY UPLC/TripleQuad5500 (Waters/AB Sciex) which have characteristics of high accuracy specificity and sensitivity. We guarantee accurate analysis of bioamine even in low abundance. With our optimized sample preparation methods... read more
shirley, NY USA, Accord
Protein methylation is a post-translational modification process in which proteins are modified by an addition of methyl groups by S-adenosylmethionine dependent methyltransferases with S-adenosyl methionine (SAM) as the primary donor of methyl group.... read more
Protein methylation is a post-translational modification process in which proteins are modified by an addition of methyl groups by S-adenosylmethionine dependent methyltransferases with S-adenosyl methionine (SAM) as the primary donor of methyl group.... read more
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