Introduction:
“Cell culture is a process in we culture cells in the laboratory i.e. in vitro, on a suitable medium containing essential nutrients under the controlled conditions.”
Thus, it is a process in which we grow cells artificially. There are different conditions for the different cell type. But the artificial medium as well as the substrate or medium that provides nutrient is the essential supplies. Cell cultures also require growth hormones, gases and physio-chemical regulators like pH buffer, osmotic pressure and temperature. Some cells require solid artificial media while other requires liquid culture media also known as suspension culture. There are mainly two types of culture:
a) Plant tissue culture
b) Animal tissue culture
Now-a-days,
…show more content…
Organotypic culture:
It is culturing of cells that retain their structure and function in the culture. In this type different cell types are used to produce a more define tissue or organ.
Histotypic culture:
This refers to the culturing of cells that will re-aggregate in to the culture and produce a three dimensional structure that is different from the tissue from which it is derive.
Primary culture:
The culture in which cells or tissues are directly taken from the organism is called primary culture.
• Cells are heterogeneous
• Slow growing
• Have same properties as of their original tissues.
Cell lines:
Cell lines are produce when primary cultures are sub-culture. There are two types of cell lines.
Continues cell line: A cell line in which there is infinite growth of cells after sub-culturing.
Finite cell line: A cell line in which cell death after sub-culturing.
Minimal requirement for animal-cell culture:
• Aseptic conditions (Clean and sterile area)
• Microbiology laboratory
• Animal house
• Facilities like equipment, liquids, chemicals and glassware
Components of media:
• Carbon source
• Phenol red dye
•
Identification of bacteria within Unknown Culture #21 In this experiment, an unknown culture of two different types of bacteria was assigned to each person, a number of tests were performed to isolate and identify these bacterial cells. Based on knowledge from the previous experiments completed in lab, a basic understanding of each type of bacteria was used to create a flow chart that would aid the process of identifying the unknown bacteria within the culture. A gram stain that is performed initially will narrow down the types of tests certain bacteria will and will not respond to. In addition to the gram stain, some of the tests that were used include, a catalase test, an Eosin methylene blue (EMB) agar test, a bile esculin test, and a 6.5% sodium chloride (NaCl) test.
Name: Avishak Deb Roy Partners: Leevell Penn, Varugh, Butler Bio 101 Lab Report #1 02.22.2018 Swimming speed of paramecium tetraurelia in different levels of treatment. Introduction Paramecia is a unicellular Protista which are naturally found in aquatic habitats. It is easily cultured in the laboratory. It is oblong shaped and covered with short hairy structure called cilia. Paramecia does not pose any health or ethical concerns and the population can be maintained if there is a food source such as Enterobacter (Biological Foundation 7).
Research is very significant, and can not be done without the use of cells and tissues. It is very critical to find cells that can be tested on, and once these cells are found, they are vital to keep.
Then they are shocked with a calcium chloride solution that changes the charge on the cell membrane so that the plasmid DNA may be accepted into the cell. This solution must be chilled so that the cell membrane may heal. After incubating the bacterial cells, they are heat shocked to open the pores in the cell membrane to allow the transformation to occur. After being chilled again in order not to melt the agar, the cells are placed in a medium
n this lab, there were four objectives needed to be met. The first one was to perform a genetic transformation procedure, the second was to move genes from one organism to another using a plasmid as a vector, and the third was to manipulate tools of biotechnology. The bacteria E. coli was used to manipulate and transform. The E. coli would be tested for ampicillin resistance and a green fluorescent glow. One hypothesis made for this lab was that the bacteria that developed a resistance to ampicillin would reproduce even in the presence of the ampicillin.
These cells became the foundation for many modern cell culture methods and other scientific discoveries,
In recent years, there has been and still is much debate over stem cell cloning and its applications. The topics of embryonic stem cells and human cloning are very large and very controversial issues that have many facets to them, and these also tend to be the issues that overshadow the smaller, less heated topics of therapeutic cloning and animal reproductive cloning. Both therapeutic cloning with its hypothetical use in medicine and animal reproductive cloning with its potential to revive extinct species are gallant undertakings, yet both sides also have their share of fallacies and drawbacks. Therapeutic cloning, or somatic cell nuclear transfer, is in essence the process of substituting the nucleus of an egg for that of the genetic material of the organism being cloned.
The structure of the cell was very visible when using the anti-tubulin. When observing the anti-actin the microfilaments were visible. The actin filaments were much thinner than those of the microtubules. The actin filaments were best observed in the periphery of the cell compared to those of the tubulin, which are spread throughout the cell because they help stabilize the cell. The TRITC dyed cells depict better the whole structure of the cell, the nucleus is more visible than those that are dyed with FITC.
Task 2 4 main tissue types Epithelial tissue: this type of tissue covers the entire surface of the human body and is made up of very closely packed cells that are either one or more layers thick. Epithelial tissue also covers or lines the internal body surfaces. There are two different types of epithelial tissue these are simple epithelium or stratified epithelium. Simple epithelium is only one cell thick whereas stratified epithelium is two or more cells thick.
Monica A Smith Tuesday at 1 p.m. Microbiology Lab Fall 2015 Page Break Introduction: In knowing why it is important to understand how to identify an organism it is best explained by helping the person preforming the test identify the patients treatment options and plan. Also helps in understanding the organism in detail and how it can be identified in the future versus similar organisms. Materials and Methods: Two unknowns where received by the instructor unknown K and C. using the methods learn in lab for identifying them.
Selective medium involves medium with environmental conditions that specifically grows some microbes while inhibiting others. Differential medium is used to identify and differentiate (as the title says) closely related microbes based on growth responses and physical indicators. It is imperative to use laboratory positive and negative controls in identifying the unknown because it confirms and compares the results of the unknown’s response to the definite guide. While performing the procedures in this report, students had to keep the bacterial and biological species concepts in context. The bacterial species concept is the identification and naming of microbes based on relating physical and physiological features of the unknown to the fitting taxa.
As technology advances, more things become possible. One of these things is genetically modifying a baby, this is very wrong. Genetic modifying or genetic engineering is altering someone or something’s DNA. Scientists hope to cure diseases with this method, but doing this can lead to some harmful effects. This process is very unethical.
Artificial tissues such as skin are formed using stem cells in the laboratory. As a case in point, in 1990, Gary Stakemiller, an electrician in Orlando received a skin transplant made of skin that was grown in a laboratory (Ricks). Stakemiller needed this graft because over a month earlier, he received burns on seventy five percent of his body (Ricks). The new skin was produced by using a “starter” medium which grows in a laboratory from cells into usable skin (Ricks). It takes about three weeks to grow each sheet of skin from cells, proteins, and nutrients (Ricks).
Joshua Miller 12/18/17 Fermentation Lab report Introduction The term fermentation refers to the chemical breakdown of a substance by bacteria, yeasts, or other microorganisms, typically involving effervescence and the giving off of heat (wikipedia). Sugars are converted to ethyl alcohol when fermentation happens. In this experiment we determined if yeast cells undergo fermentation when placed in a closed flask with no oxygen. Glucose and yeast are mixed together in a closed flask and allowed to incubate for about one hour.
Conclusion and Recommendations Ultimately, testing cell viability and knowing the count of viable and non-viable cells in a cell line is an important key in any research using cells. Having enough number of viable cells in a suspension would give accurate results in an experiment. This also shows how trypan blue is an important dye in cell viability and in the study of cells. This dye makes researcher’s life convenient in identifying and differentiating viable versus non-viable cells or live versus dead cells. It is really needed that researchers should ensure new and fresh cell cultures to ensure more viable cells in a culture.