A fluorescent method for countingBabesia, Anaplasma, PlasmodiumandTrypanosomafollowing DNA staining with 33258 Hoechst (Bisbenzimide)

1981 ◽  
Vol 75 (2) ◽  
pp. 123-129 ◽  
Author(s):  
B. J. Rodwell ◽  
R. J. Howard
2021 ◽  
Vol 26 ◽  
pp. 100954
Author(s):  
Avani Mehta ◽  
Prateek Raj ◽  
Sandeep Sundriyal ◽  
Balasubramanian Gopal ◽  
Umesh Varshney

1978 ◽  
Vol 53 (6) ◽  
pp. 321-330 ◽  
Author(s):  
H. A. Crissman ◽  
A. P. Stevenson ◽  
D. J. Orlicky ◽  
R. J. Kissane
Keyword(s):  

2003 ◽  
Vol 320 (2) ◽  
pp. 292-298 ◽  
Author(s):  
Maria J Vazquez ◽  
Beatriz Rodriguez ◽  
Cleofe Zapatero ◽  
David G Tew

Life Sciences ◽  
1995 ◽  
Vol 57 (18) ◽  
pp. 1701-1707 ◽  
Author(s):  
J.Clay Isbell ◽  
Samuel T. Christian ◽  
Nicole A. Mashburn ◽  
P.Darwin Bell

PEDIATRICS ◽  
1972 ◽  
Vol 50 (4) ◽  
pp. 625-631
Author(s):  
Larry P. Kammholz ◽  
L. Gilbert Thatcher ◽  
Frederic M. Blodgett ◽  
Thomas A. Good

A rapid fluorescent method for estimation of free erythrocyte protoporphyrin (FEP) is described. Simple ethyl acetate-glacial acetic acid extractions are performed, fluorescence quantitated in a fluorimeter and expressed numerically by comparison with known coproporphyrin standards. Fifty-six children were studied and the extent of lead poisoning was evaluated initially and at different follow-up intervals. A clear relationship was shown between FEP fluorescence and blood lead levels. A correlation was also seen for the intensity of fluorescence and evidence for increased absorption of lead, as estimated by x-ray evidence of ingested lead and deposits in bone. Children with iron deficiency anemia also showed elevations of FEP fluorescence. This FEP fluorescence test allows for a rapid, numerical determination which appears to be useful as a screening test for lead intoxication. It can quickly select patients that may have markedly increased lead absorption and need prompt therapy or select those that at least require further studies for possible lead exposure or the presence of anemia.


2018 ◽  
Vol 1124 ◽  
pp. 031012
Author(s):  
M V Mekhrengin ◽  
I K Meshkovskii ◽  
L A Kaftyreva ◽  
V I Guryev ◽  
D A Pogorelaya

2010 ◽  
Vol 73 (10) ◽  
pp. 1659-1666 ◽  
Author(s):  
Wei-luen Yu ◽  
Gianni Guizzunti ◽  
Timothy L. Foley ◽  
Michael D. Burkart ◽  
James J. La Clair

1975 ◽  
Vol 39 (1) ◽  
pp. 145-149 ◽  
Author(s):  
M. E. Katora ◽  
T. M. Hollis

A quantitative system for direct protein tracing and measurement of net protein uptake in the aorta using fluorescein isothiocyanate conjugated bovine serum albumin (FITCBSA) is described. Using Wistar rats, a mean aortic FITCBSA net uptake of 29.7 times 10(-17) g FITCBSA per mum2 aortic endothelial surface area per 24 h was obtained. Intra-aortic localization of the FITCBSA was observed along the endothelium and the collagen-elastin bands. The values obtained using this FITCBSA system are comparable with those of a previously established isotopic technique measuring aortic albumin flux and reconfirm the previous findings of the existence of an albumin permeability gradient in the thoracic aorta.


Author(s):  
Mani Krishna ◽  
Adesh Kumar

<p class="abstract"><strong>Background:</strong> Tuberculosis is infectious disease caused by <em>Mycobacterium tuberculosis</em>. There are various methods for diagnosis of tuberculosis such as direct clinical material examination of tubercular bacilli by Ziehl – Neelsen (ZN) staining, demonstration of tubercular bacilli by auramine – rhodamine (AR) staining and autofluorescence (AF).</p><p class="abstract"><strong>Methods:</strong> Present study was done clinically suspected tubercular patients. All received samples Zn stain, fluorescent stain and PAP stain were applied.</p><p class="abstract"><strong>Results:</strong> Among the clinically suspected patients 88 was diagnosed with tuberculosis. Female preponderance was noted accounting for 60.23% (53/88) of cases. Of the 88 aspirates, the smear positivity for acid fast bacilli (AFB) on the ZN method was 37.5% (33/88) while the positivity increased to 81.82% (72/88) on the AR fluorescent method and 86.36% (76/88) on AF.</p><strong>Conclusions:</strong> AF staining is more sensitive than the auramine – rhodamine fluorescent and ZN staining in demonstration of mycobacterium bacilli in fine needle aspiration cytology of tubercular lymphnode.


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