Sickle cell disease
Hemoglobin
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Proteins are produced as polymer of amino acid chains. They gain secondary structure elements such as alpha helix, beta sheet during folding and for their three dimensional structure. Some proteins such as Hemoglobin make quaternary structure where they form the final structure with four different subunits of two different proteins interacting each other.
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Red blood cells carry oxygen fro the lungs to the body cells. A red blood cell is made mostly of hemoglobin. Hemoglobin is an iron-containing protein that binds chemically to oxygen molecules. Red blood cells are produced in the bone marrow and have no nuclei.
Hemoglobin produced in association with the sickle cell trait; the beta-globin molecules of hemoglobin S are defective.
it is produced by interstitial fibroblasts in the kidney in close association with peritubular capillary and tubular epithelial cells
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Biliverdin
transcription
Transcription.
hemoglobin is found in red blood cells. Oxygen binds to hemoglobin which is composed of four iron particulates.
Hemoglobin
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There are two categories of hemoglobinopathy. In the first category, abnormal globin chains give rise to abnormal hemoglobin molecules. In the second category, normal hemoglobin chains are produced but in abnormal amounts.
actually it's not recycled but the haemoglobin will die after 120 days. haemoglobin are produced from bone marrow
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