scholarly journals Laboratory Organization

Laboratory organization involves both the physical establishment and its operation. It is perhaps simplest to divide the laboratory into its component sections and discuss each separately. The areas may physically overlap for a small facility, and depending on the operation specialty, some sections, such as tissue culture or probe amplification, may not be required. Unless the operation is large, dark room and cold room facilities and expensive equipment such as an ultracentrifuge and beta counter are best shared, if feasible. The setup of a DNA analysis facility is a relatively simple process if it is incorporated into an established biochemistry program; it is considerably more involved if no such base exists. The outline presented in this chapter is only a guide; individuals contemplating the development of a new facility should visit as many established centers as possible. Discussions with sales representatives and attendance at relevant trade shows and DNA conferences are invaluable. Office requirements for a DNA program are no different in principle from those of any other biochemistry program. At least one separate office is required, usually for the program director and, as space permits, offices for a clerk-secretary and senior technologist are useful. Everyone working in the laboratory must have at least a small partitioned desk space in a quiet location. Lockable fire-resistant cabinets are required to store sensitive records; these cabinets should be accessible, preferably located in the clerical area. Analysis results are worthless without proper documentation of a specimen’s chain of custody (continuity). Information, including time and conditions of specimen procurement, conditions of storage and shipment, date received by the laboratory, and reason for the analysis request is also required. These data can be manually recorded; however, entry into a computer program capable of sorting and maintaining records for long-term retrieval is almost mandatory. Storage of unprocessed specimens may be necessary, and if at all possible, DNA should be isolated when received.

1989 ◽  
Vol 65 (4) ◽  
pp. 1125-1135 ◽  
Author(s):  
J G De Mey ◽  
M P Uitendaal ◽  
H C Boonen ◽  
M J Vrijdag ◽  
M J Daemen ◽  
...  

Author(s):  
W. Sloterdijk ◽  
M. Hommes

In today’s challenging environment, the priority for many oil and gas operation companies is to design, build and safely operate facilities at optimum cost efficiency. This means that new facility designs must consider critical facility integrity and that existing facilities are operated well beyond their intended design life. Main gas transmission systems are now some 50 years old and operate for longer periods than anticipated during design and construction for reasons such as; the transition to renewables with another 50 years of service foreseen, and; gas transmission systems that operate satisfactorily, have very low failure rates and for which the planned safe life time extension is expected to be the lowest cost option.


1956 ◽  
Vol 63 (1) ◽  
pp. 52-58
Author(s):  
VERNON P. PERRY ◽  
VIRGINIA J. EVANS ◽  
WILTON R. EARLE ◽  
GEORGE W. HYATT ◽  
WALLACE C. BEDELL
Keyword(s):  

Author(s):  
Jenna M. Loyd ◽  
Alison Mountz

Chapter 3 examines how central Louisiana became the unlikely site for the Immigration and Naturalization Service’s first new long-term detention facility and hub for deportation. Faced with high unemployment following the collapse of the local lumber industry, the enterprising mayor of Oakdale spearheaded a campaign to secure the new federal facility. Simultaneously, the Department of Justice debated which agency was best suited to carry out the new mandate of long-term detention of noncitizens. The INS did not have the carceral experience of the Bureau of Prisons, but because migrant detention was not a criminal justice punishment, this imprisonment threatened to create legal liabilities for the government. These legal questions also informed jurisdictional conflict over where this new facility would be sited. Oakdale’s efforts were jeopardized as Associate Attorney General Rudolph Giuliani backed the proposal of the Bureau of Prisons to run migrant detention near one of its prisons in Oklahoma. The forceful backing of Louisiana politicians eventually won the facility for Oakdale.


Plants ◽  
2020 ◽  
Vol 9 (8) ◽  
pp. 929
Author(s):  
Carloalberto Petti

Tissue culture is an essential requirement in plant science to preserve genetic resources and to expand naturally occurring germplasm. A variety of naturally occurring and synthetic hormones are available to induce the processes of dedifferentiation and redifferentiation. Not all plant material is susceptible to tissue culture, and often complex media and hormone requirements are needed to achieve successful plant propagations. The availability of new hormones or chemicals acting as hormones are critical to the expansion of tissue culture potentials. Phloroglucinol has been shown to have certain hormone-like properties in a variety of studies. Ornithogalum dubium, an important geophyte species, was used to characterise the potential of phloroglucinol as the sole plant-like hormone in a tissue culture experiment. Tissue culture, plant regeneration, total phenolic and genetic variability were established by applying a variety of methods throughout long-term experiments. Phloroglucinol did induce callus formation and plant regeneration when used as the sole supplement in the media at a rate of 37%, thus demonstrating auxin/cytokines-like properties. Callus formation was of 3 types, friable and cellular, hard and compact, and a mixture of the two. The important finding was that direct somatogenesis did occur albeit more frequently on younger tissue, whereby rates of induction were up to 52%. It is concluded that phloroglucinol acts as a “hormone-like” molecule and can trigger direct embryogenesis without callus formation.


2019 ◽  
Vol 188 (3) ◽  
pp. 839-847
Author(s):  
Megumu Tsujimoto ◽  
Hiroshi Kagoshima ◽  
Hiroshi Kanda ◽  
Kenichi Watanabe ◽  
Satoshi Imura

Abstract Studies on the long-term survival of animals often focus on the specific instance of survival of animals only, and descriptions of subsequent reproduction are generally not reported. In this study, we recorded the reproductive performance of the first-generation offspring of the resuscitated individual (SB-1) and the hatchling of the resuscitated egg (SB-3) of the Antarctic tardigrade, Acutuncus antarcticus, after being frozen for 30.5 years. By providing further detailed description of the reproduction of SB-1 and SB-3 after revival, and then comparing the reproductive performance with that of their first-generation offspring, the possible indications of the damage accrued during the long-term preservation in SB-1 and SB-3 were more specifically detected. Additionally, the DNA analysis revealed two distinctively different mitochondrial genetic sequences of A. antarcticus between the SB strains and the LSW strain. The observed differences in some of the reproductive parameters between the two genetic types suggested a possible relationship between the life-history traits and genetic type in the species A. antarcticus. Further experiments using the SB-1 and SB-3 strains reared for a long period to exclude the instant effect of preservation are expected to improve our understanding of the mechanisms underlying the long-term survival of animals.


2005 ◽  
Vol 141 (1) ◽  
pp. 21-27 ◽  
Author(s):  
Martin Marsala ◽  
Osamu Kakinohana ◽  
Michael P. Hefferan ◽  
Dasa Cizkova ◽  
Kiyohiko Kinjoh ◽  
...  

1997 ◽  
Vol 152 (1) ◽  
pp. 59-67 ◽  
Author(s):  
Y H A Abdel-Wahab ◽  
F P M O'Harte ◽  
C R Barnett ◽  
P R Flatt

Abstract Characteristics of cellular insulin glycation were examined in the pancreatic B-cell line, BRIN-BD11. The extent of insulin glycation increased stepwise during 72 h of culture at 5·6–33·3 mmol/l glucose, attaining levels up to 27%. Glycation of insulin at 33·3 mmol/l glucose was rapid, reaching maximal values within 2 h, and not readily reversible during 2 to 24 h of subsequent exposure to 5·6 mmol/l glucose. Glycated insulin was readily secreted by BRIN-BD11 cells upon active stimulation with glucose and other secretagogues. Cellular insulin glycation was decreased by 66–80% by inhibitors of protein glycation, vitamin C, aminoguanidine or acetylsalicylic acid. Modulation of insulin-secretory activity of BRIN-BD11 cells by co-culture at high glucose with diazoxide, l-alanine or glibenclamide indicated that long-term stimulation of secretion was associated with a decrease in the extent of insulin glycation. Glycation of insulin in vitro was substantially less extensive than in BRIN-BD11 cells, although glucose-6-phosphate and glyceraldehyde-3-phosphate were 1·4- to 2·0-fold more reactive than glucose per se. These observations indicate that insulin is readily glycated and secreted from insulin-secreting cells under hyperglycaemic conditions in culture. Journal of Endocrinology (1997) 152, 59–67


1968 ◽  
Vol 22 (4) ◽  
pp. 798-807 ◽  
Author(s):  
G C Schild ◽  
J S Oxford ◽  
C W Potter

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