Identification of Rock-Wallabies, Petrogale-Penicillata (Gray, 1825), From the Grampians, Victoria, and Comparison With Conspecifics by Examination of Chromosomes, Blood Proteins, Cell-Surface Antigens, Parasites and Morphology

1988 ◽  
Vol 36 (1) ◽  
pp. 99 ◽  
Author(s):  
RL Close ◽  
S Ingleby ◽  
RAH Vanoorschot ◽  
AA Gooley ◽  
DA Briscoe ◽  
...  

Two rock-wallabies were captured in the Victoria Range of the Grampians, the first specimens obtained from Victoria for scientific study. Their chromosomes identified them as Petrogale penicillata and, although the animals appeared to be smaller than their nearest studied conspecifics from Jenolan Caves, N.S.W., 800 km to the north-east, analysis of blood proteins, red blood cell epitopes and parasites indicated little genetic divergence. This lack of differentiation is unusual in a genus in which, further north along the Great Dividing Range, nine chromosomally distinct forms occur within 1500 km. One animal was heterozygous for presence and absence of a major C-band on the second largest chromosome; chromosomes without this band have not been found in other mainland P. penicillata. No electrophoretic variation was detected at 23 genetic loci, even though one allele was unique among P. penicillata so far studied. Although only one extant colony was found, other disused sites were located 30 km further north. Despite the apparent low numbers of animals, there is some evidence that additional colonies may be found.

2018 ◽  
Vol 9 (5) ◽  
pp. 91-95 ◽  
Author(s):  
Praveen Kumar Vemuri ◽  
Sanjay Madala ◽  
Vijaya Lakshmi Bodiga ◽  
Suryanarayana Veeravalli ◽  
Nithin Chand Kurra

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Éva Sautner ◽  
Krisztián Papp ◽  
Eszter Holczer ◽  
Eszter L. Tóth ◽  
Rita Ungai-Salánki ◽  
...  

Vox Sanguinis ◽  
2009 ◽  
Vol 96 (2) ◽  
pp. 153-156 ◽  
Author(s):  
G. Daniels ◽  
L. Castilho ◽  
W. A. Flegel ◽  
A. Fletcher ◽  
G. Garratty ◽  
...  

Author(s):  
K. Chien ◽  
I.P. Shintaku ◽  
A.F. Sassoon ◽  
R.L. Van de Velde ◽  
R. Heusser

Identification of cellular phenotype by cell surface antigens in conjunction with ultrastructural analysis of cellular morphology can be a useful tool in the study of biologic processes as well as in diagnostic histopathology. In this abstract, we describe a simple pre-embedding, protein A-gold staining method which is designed for cell suspensions combining the handling convenience of slide-mounted cell monolayers and the ability to evaluate specimen staining specificity prior to EM embedding.


1993 ◽  
Vol 16 (10) ◽  
pp. 1054-1056
Author(s):  
Dai SASAKI ◽  
Satoshi KOSUNAGO ◽  
Takeshi MIKAMI ◽  
Tatsuji MATSUMOTO ◽  
Masuko SUZUKI

1971 ◽  
Vol 134 (4) ◽  
pp. 857-870 ◽  
Author(s):  
Darcy B. Wilson ◽  
Dianne H. Fox

The proliferative reactivity of lymphocytes from rat donors maintained under germfree or conventional conditions was examined in mixed lymphocyte cultures stimulated with allogeneic and xenogeneic cell surface antigens. The results show (a) that lymphocytes from conventionally maintained rats are less reactive to human, hamster, guinea pig, and mouse cell surface antigens than to the major H alloantigens, and (b) that lymphocytes from germfree rats display no demonstrable reactivity to xenogeneic cells, but are quantitatively normal in their response to allogenic cells. The conclusion drawn from these observations is that the circulating lymphocyte pool of an individual consists of a greater proportion of cells reactive to H alloantigens of other members of the same species than to the xenogeneic cellular antigens of members of other species and that this large number of cells is not generated by a mechanism involving immunization to cross-reactive environmental antigens.


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