Biochemistry

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Peptide mass fingerprinting (PMF) is an investigative method for protein distinguishing proof.

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Creative Proteomics gives Shotgun proteomics benefit in light of ID and measurement of peptides from processed proteins utilizing couple mass spectrometry.

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Protein phosphorylation is the most ordinarily contemplated region of post-translational adjustment.

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Peptidomics, characterized as the precise, far reaching, subjective/quantitative multiplex examination of endogenous peptides (up to ~20 kDa).

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In the quantitative proteomics investigate, a few MS-based approachs for relative measurement have been presented for examination of various

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Established by irradiation of the adherent cells in long-term bone marrow cultures derived from C3H/HeNSlc strain mice and MS-5.

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Bone marrow cells are the cells contained within the bone marrow. These include stromal cells, which are not directly involved in haematopoiesis, and haematopoietic stem cells.

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The gallbladder is a hollow organ that sits just beneath the right lobe of the liver. The gallbladder cells from Creative Bioarray are isolated from human gallbladder tissue.

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Peptide de novo sequencing is the analytical process that derives a peptide’s amino acid sequence from its tandem mass spectrum (MS/MS) without the assistance of a sequence database.

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If an exact knowledge of protein/peptide quantities is required for further applications, quantitative amino acid analysis.

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For many proteins and peptides, disulfide bridges are prerequisite for their proper biological function.

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In the quantitative proteomics research, several MS-based methodologies for relative quantification have been introduced for comparison of different proteomes from collected biological samples.

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Gas Chromatography (GC) is an analytical technique for a wide variety of volatile and/or semi-volatile organic compounds identification and quantitation.