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The clear epidermal cells exist in a single layer and do not contain chloroplasts, because the onion fruiting body (bulb) is used for storing energy, not photosynthesis. [3] Each plant cell has a cell wall, cell membrane, cytoplasm, nucleus, and a large vacuole. The nucleus is present at the periphery of the cytoplasm.
An example of a Lineweaver–Burk plot of 1/v against 1/a In biochemistry , the Lineweaver–Burk plot (or double reciprocal plot ) is a graphical representation of the Michaelis–Menten equation of enzyme kinetics , described by Hans Lineweaver and Dean Burk in 1934.
Functions of the form = have at most one -intercept, but may contain multiple -intercepts. The x {\displaystyle x} -intercepts of functions, if any exist, are often more difficult to locate than the y {\displaystyle y} -intercept, as finding the y {\displaystyle y} -intercept involves simply evaluating the function at x = 0 {\displaystyle x=0} .
A calibration curve plot showing limit of detection (LOD), limit of quantification (LOQ), dynamic range, and limit of linearity (LOL).. In analytical chemistry, a calibration curve, also known as a standard curve, is a general method for determining the concentration of a substance in an unknown sample by comparing the unknown to a set of standard samples of known concentration. [1]
In Chara coralina, cells can grow up to 10 cm long and 1 mm in diameter. [8] The diameter of the vacuole can occupy around 80% of the cell's diameter. [11] Thus for a 1 mm diameter cell, the vacuole can have a diameter of 0.8 mm, leaving only a path width of about 0.1 mm around the vacuole for cytoplasm to flow.
The earliest reference to the use of conoscopy (i.e., observation in convergent light with a polarization microscope with a Bertrand lens) for evaluation of the optical properties of liquid crystalline phases (i.e., orientation of the optical axes) is in 1911 when it was used by Charles-Victor Mauguin to investigate the alignment of nematic and ...
Moiré Effect. Structured illumination microscopy (SIM) is a method of super-resolution microscopy which is performed by acquiring multiple images of the same sample under different patterns of illumination, then computationally combining these images to achieve a single reconstruction with up to 2x improvement over the diffraction limited lateral resolution.
A scanning transmission electron microscope (STEM) is a type of transmission electron microscope (TEM). Pronunciation is [stɛm] or [ɛsti:i:ɛm]. As with a conventional transmission electron microscope (CTEM), images are formed by electrons passing through a sufficiently thin specimen. However, unlike CTEM, in STEM the electron beam is focused ...