Complete organs are often placed in containers filled with NBF. Although formalin penetrates quite quickly, for a while it will not reach the center of a large mass, and the delay can allow some autolysis in the middle of the tissue. Large organs should be described as soon as possible, and then cut into slices about 1 cm in size so that the fixator can access them. Similarly, the intestine should be opened and cleaned of any contents, then turned over into a container large enough for the fixator to touch all tissue surfaces, or pinned to a board with stainless steel pins and placed in the fixator. 10% neutral buffered formalin is a general histological tissue fixative and a standard fixative for use in a diagnostic environment. Phosphates buffered in formalin adjust the pH to about 7.0, as the “neutral” phosphate closes. The neutral pH value inhibits the formation of “formalin pigment”. Neutral buffered formalin, usually simply abbreviated as NBF, has become the standard fixative for use in a diagnostic environment. It is more effective than simple formalin mixtures because the phosphate salts present make it unlikely that erythrocytes will be damaged, and the neutral pH inhibits the formation of formalin pigment. Phosphates adjust the pH to about 7.0, as the “neutral” moon suggests, but there`s no need to be ultra-precise if it`s slightly different. Although the formation of formalin pigment is inhibited, it is not completely stopped and can form slowly in very bloody tissues or in tissues stored in NBF for a long time without it being altered.
In practice in a diagnostic laboratory, the slowness of the simple fixation of formalin is a significant disadvantage. If the limitations of a diagnosis are a major problem, consider increasing the temperature of the fixative solution. It should be noted that although an increase in the temperature of the fixative can increase the rate of fixation, this leads to a decrease in the quality of the final colored section, and there may also be effects on certain coloring or immunohistochemical reactions. The increase in temperature must be kept to a minimum in order to achieve the goal of faster fixation, since heat itself is a means of fixation. When high temperatures are used, formaldehyde vapors are produced, especially when the temperature is high, so the fixation must be carried out in an exhaust chamber to protect the personnel. 10% neutral buffered formalin (NFB) is a general histological tissue fixative. Contains formaldehyde buffered at a neutral pH. Our NFB is designed ready to use and should not require any additives.
Secondary fixation Other fixatives can be applied after formalin fixation, and some of their properties are preserved. It must be recognized that the secondary fixation in a fixative does not give the same results as it would have been obtained if the secondary fixative had been applied to fresh tissues. Time This fixative should be used at least overnight, but the fixation is only finished for a few days and a week or two is not too long. For complete fixation, proteins in the tissue must be cross-linked, but simple formalin mixtures are known to discolor tissues long before the proteins are relocated. For this reason, visual observation does not give an indication of the degree of fixation and discoloration should never be used as an indicator that it is complete. 10% neutral buffered formalin is a general histological tissue fixative. Formalin consists of formaldehyde (37 to 40% (w/v)), with 10% neutral buffered formalin (NBF) essentially a 4% formaldehyde solution (v/v) diluted with a pH neutral phosphate buffer. 10% NBF is a commonly used general purpose histological fixator often used in sample preparation for optical microscopy.
It is ideal for short-term sample fixation, but is equally effective for long-term tissue storage and compatible with targets such as proteins, peptides, and small molecule enzymes. Our 10% NBF solution is specially designed for use in multiple histological and cytological applications. The product has a neutral pH and is delivered without impurities, minimizing discomfort caused by background stains and non-specific artifacts. 10% NBF forms cross-links between the aldehydes and proteins of the study samples, which maintain the original structure of the cellular components and prepare the samples for successive processing and staining operations. The sale on a small vial contains 40 ml with label for data samples. It is important that the fixation time is noted and sufficient time is given for the appearance of chemical reactions. The time measured in a few hours is not enough and the absence of cross-linking in the treated tissues for such a short time does not give the fabric sufficient protection against the binding effects of desiccant ethanols. Small pieces of fabric do not attach much faster than larger pieces. Fine needle biopsies require the same amount of time as 3 mm thick slices of solid organs. NBF is useful as a fixator for museum and photo samples, as it allows the restoration of the natural color of the specimen. 10% neutral buffered formalin (4% neutral buffered formaldehyde) Our team of scientists has experience in all areas of research, including life sciences, materials science, chemical synthesis, chromatography, analysis and many more. Properties: • Used for fixing and storage of different types of tissues • Prevents excessive removal or hardening of samples • Supplied as a ready-to-use solution • Standard fixative for histological applications.
Looking for similar products? To the product comparison guide Molecular weight: 30.026 g/mol Molecular formula: CH2O Form: Colourless liquid Synonyms: Formaldehyde, formalin, methanol, formalin InChI key: WSFSSNUMVMOOMR-UHFFFAOYSA-N Storage: Ambient temperature Tissues can be stored in this solution for a long time, but the fixator must be changed at least every six months. Tissue samples should be placed immediately in the NFB to prevent autolysis, rot and other unwanted cell changes. If necessary, the circulation of the whole body must be carried out to ensure adequate fixation of the cellular level (see the appendix file). . Post-treatment NBF contains salts that are only partially soluble in high concentrations of ethanol. For this reason, the tissues must be transferred into a dehydrogenator containing 60% ethanol or less for a short time to give the salts the opportunity to be removed. .