Infrared (IR) Spectroscopy – Definition, Principle, Instrumentation, Applications, Advantages & Limitations

Infrared (IR) Spectroscopy – Definition, Principle, Instrumentation, Applications, Advantages & Limitations

Infrared (IR) Spectroscopy, also called Vibrational Spectroscopy, is an analytical technique that studies the interaction of infrared radiation with matter.

NMR Spectroscopy – Definition, Principle, Instrumentation, Working, Applications, Advantages & Limitations

NMR Spectroscopy – Definition, Principle, Instrumentation, Working, Applications, Advantages & Limitations

NMR Spectroscopy (Nuclear Magnetic Resonance Spectroscopy) is one of the most advanced and widely used analytical techniques in modern chemistry and biology.

Paper Chromatography – Definition, Principle, Types, Steps, Applications, Advantages & Limitations

Paper Chromatography – Definition, Principle, Types, Steps, Applications, Advantages & Limitations

Paper Chromatography (PC) is a form of planar chromatography where the separation takes place on a specialized filter paper. Learn its definition, principle, types, steps, Rf values, applications, advantages, and limitations in detail.

Gamma-ray Spectroscopy – Definition, Principle, Instrumentation, Applications, Advantages & Limitations

Gamma-ray Spectroscopy – Definition, Principle, Instrumentation, Applications, Advantages & Limitations

Gamma-ray spectroscopy (GRS) is a technique that measures the energy distribution of gamma rays emitted by a radioactive sample. By analyzing this spectrum, scientists can identify and quantify specific isotopes present in the material.

UV Spectroscopy – Definition, Principle, Instrumentation, Steps, Applications, Advantages & Limitations

UV Spectroscopy – Definition, Principle, Instrumentation, Steps, Applications, Advantages & Limitations

UV Spectroscopy is an analytical technique that studies how molecules absorb ultraviolet light. Learn the definition, principle, types of electronic transitions, instrumentation, steps, uses, advantages, and limitations of UV spectroscopy in detail.

X-Ray Spectroscopy – Definition, Principle, Working, Instrumentation, Applications, Advantages & Limitations

X-Ray Spectroscopy – Definition, Principle, Working, Instrumentation, Applications, Advantages & Limitations

X-Ray Spectroscopy is a powerful analytical technique used to identify and study materials by their X-ray emissions. Learn its principle, parts, working, applications, advantages, and limitations in detail.

Gel Filtration Chromatography (GFC) – Definition, Principle, Types, Steps, Applications, Advantages & Limitations

Gel Filtration Chromatography (GFC) – Definition, Principle, Types, Steps, Applications, Advantages & Limitations

Gel Filtration Chromatography (GFC), also known as Size Exclusion Chromatography, is a separation technique used to isolate biomolecules based on size. Learn its principle, parts, steps, types, uses, advantages, and limitations in detail.

Gel Permeation Chromatography (GPC) – Definition, Principle, Instrumentation, Steps, Applications, Advantages & Limitations

Gel Permeation Chromatography (GPC) – Definition, Principle, Instrumentation, Steps, Applications, Advantages & Limitations

Gel Permeation Chromatography (GPC), also called Size Exclusion Chromatography (SEC) or Gel Filtration Chromatography, is a powerful separation technique widely used in biochemistry, biotechnology, and polymer science.

Flow Cytometry – Definition, Principle, Steps, Types, Applications, Advantages & Limitations

Flow Cytometry – Definition, Principle, Steps, Types, Applications, Advantages & Limitations

Flow cytometry is a powerful analytical technique widely used in biology, medicine, and research labs to study cells and particles in a fluid suspension.

Polyacrylamide Gel Electrophoresis (PAGE) – Principle, Procedure, Applications, Advantages & Limitations

Polyacrylamide Gel Electrophoresis (PAGE) – Principle, Procedure, Applications, Advantages & Limitations

Polyacrylamide Gel Electrophoresis (PAGE) is a laboratory technique used to separate proteins and nucleic acids based on their size and charge by making them move through a polyacrylamide gel under electricity.