Immunohistochemical Analysis of Pulmonary and Pleural Neoplasms Using a Monoclonal Antibody (47D10) Which Reacts with Nonspecific Cross-Reacting Antigen

Tumor Biology ◽  
1989 ◽  
Vol 10 (6) ◽  
pp. 281-288 ◽  
Author(s):  
J.A. Radosevich ◽  
P.G. Robinson ◽  
W.P. Carney ◽  
W. Warren ◽  
S.T. Rosen ◽  
...  
1994 ◽  
Vol 72 (05) ◽  
pp. 762-769 ◽  
Author(s):  
Toshiro Takafuta ◽  
Kingo Fujirmura ◽  
Hironori Kawano ◽  
Masaaki Noda ◽  
Tetsuro Fujimoto ◽  
...  

SummaryGlycoprotein V (GPV) is a platelet membrane protein with a molecular weight of 82 kD, and one of the leucine rich glycoproteins (LRG). By reverse transcription-polymerase chain reaction (RT-PCR), GPV cDNA was amplified from mRNA of platelets and megakaryocytic cell lines. However, since there are few reports indicating whether GPV protein is expressed in megakaryocytes as a lineage and maturation specific protein, we studied the GPV expression at the protein level by using a novel monoclonal antibody (1D9) recognizing GPV. Flow cytometric and immunohistochemical analysis indicated that GPV was detected on the surface and in the cytoplasm of only the megakaryocytes in bone marrow aspirates. In a megakaryocytic cell line UT-7, GPV antigen increased after treatment with phorbol-12-myri-state-13-acetate (PMA). These data indicate that only megakaryocytes specifically express the GPV protein among hematopoietic cells and that the expression of GPV increases with differentiation of the megakaryocyte as GPIb-IX complex.


2019 ◽  
Vol 38 (1) ◽  
pp. 18-24 ◽  
Author(s):  
Yukinari Kato ◽  
Shinji Yamada ◽  
Yoshikazu Furusawa ◽  
Shunsuke Itai ◽  
Takuro Nakamura ◽  
...  

1993 ◽  
Vol 235 (3) ◽  
pp. 335-341 ◽  
Author(s):  
Yoshihisa Fujikura ◽  
Hidehiko Ohta ◽  
Toshio Hirai ◽  
Tetsuo Fukumoto

1991 ◽  
Vol 39 (12) ◽  
pp. 1603-1610 ◽  
Author(s):  
C L Finstad ◽  
B W Yin ◽  
C M Gordon ◽  
M G Federici ◽  
S Welt ◽  
...  

Monoclonal antibodies (MAb) C219 and JSB-1 have been used extensively in the analysis of P-glycoprotein expression in normal and malignant tissues. This study demonstrates that some commercial lots of these MAb, even those supplied as purified immunoglobulins, contain contaminating anti-A blood group antibodies. In both sources of reagent, the antibody was specific for a particular A structure, known as repetitive or Type 3 A. These observations may account for earlier studies showing polymorphic variation in P-glycoprotein expression in epithelial tissues and an apparent correlation with the A blood type of the donor. Such reactivity can be eliminated by absorption of anti-P-glycoprotein reagents with A erythrocytes. These data re-emphasize the importance of evaluating MAb samples for unsuspected contaminating antibodies.


2000 ◽  
Vol 79 (9) ◽  
pp. 798-799 ◽  
Author(s):  
KAZUHIRO KAWAMURA ◽  
KAZUHIKO SEKIGUCHI ◽  
SATOSHI SHIBATA ◽  
JUN FUKUDA ◽  
HIDEYA KODAMA ◽  
...  

2020 ◽  
Vol 39 (4) ◽  
pp. 117-122 ◽  
Author(s):  
Teizo Asano ◽  
Masato Sano ◽  
Junko Takei ◽  
Yusuke Sayama ◽  
Mika K. Kaneko ◽  
...  

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