Insoluble human plasma protein immunoadsorbents. Large-scale production and storage

1977 ◽  
Vol 74 (3) ◽  
pp. 237-245 ◽  
Author(s):  
Samuel T. Nerenberg ◽  
Rameshwar Prasad ◽  
Nancy Biskup ◽  
Linda Pedersen (Demarco)
2021 ◽  
Vol 8 (3) ◽  
pp. 20210304
Author(s):  
Semyon Bachinin ◽  
Venera Gilemkhanova ◽  
Maria Timofeeva ◽  
Yuliya Kenzhebayeva ◽  
Andrei Yankin ◽  
...  

Metal-organic frameworks (MOFs), being a family of highly crystalline and porous materials, have attracted particular attention in material science due to their unprecedented chemical and structural tunability. Next to their application in gas adsorption, separation, and storage, MOFs also can be utilized for energy transfer and storage in batteries and supercapacitors. Based on recent studies, this review describes the latest developments about MOFs as structural elements of metal-ion battery with a focus on their industry-oriented and large-scale production.


2021 ◽  
Vol 703 (1) ◽  
pp. 012034
Author(s):  
L Ahonen ◽  
J Hietava ◽  
K Korhonen ◽  
A Martinkauppi ◽  
K Piipponen

Vox Sanguinis ◽  
1988 ◽  
Vol 55 (4) ◽  
pp. 202-210 ◽  
Author(s):  
C. Michalski ◽  
F. Bal ◽  
T. Burnouf ◽  
M. Goudemand

Blood ◽  
1982 ◽  
Vol 59 (3) ◽  
pp. 664-670 ◽  
Author(s):  
AH Goodall ◽  
G Kemble ◽  
DP O'Brien ◽  
E Rawlings ◽  
F Rotblat ◽  
...  

Abstract A murine hybridoma clone is described that grows continuously in culture and produces a monoclonal antibody we have called Royal Free Monoclonal Antibody to factor IX No. 1 (RFF-IX/1). This has high affinity for a coagulation site on factor IX. RFF-IX/1 immobilised on sepharose can be used to deplete factor IX from normal human plasma. This immunoaffinity depleted plasma is indistinguishable from severe Christmas disease plasma and can be used as the substrate in a one stage coagulation assay for factor IX. The affinity column has high capacity and can be regenerated so that large scale production from normal plasma of factor IX deficient plasma as a diagnostic reagent is now feasible.


Vox Sanguinis ◽  
2003 ◽  
Vol 84 (1) ◽  
pp. 54-64 ◽  
Author(s):  
K. Tomokiyo ◽  
H. Yano ◽  
M. Imamura ◽  
Y. Nakano ◽  
T. Nakagaki ◽  
...  

Blood ◽  
1982 ◽  
Vol 59 (3) ◽  
pp. 664-670
Author(s):  
AH Goodall ◽  
G Kemble ◽  
DP O'Brien ◽  
E Rawlings ◽  
F Rotblat ◽  
...  

A murine hybridoma clone is described that grows continuously in culture and produces a monoclonal antibody we have called Royal Free Monoclonal Antibody to factor IX No. 1 (RFF-IX/1). This has high affinity for a coagulation site on factor IX. RFF-IX/1 immobilised on sepharose can be used to deplete factor IX from normal human plasma. This immunoaffinity depleted plasma is indistinguishable from severe Christmas disease plasma and can be used as the substrate in a one stage coagulation assay for factor IX. The affinity column has high capacity and can be regenerated so that large scale production from normal plasma of factor IX deficient plasma as a diagnostic reagent is now feasible.


Vox Sanguinis ◽  
1962 ◽  
Vol 7 (4) ◽  
pp. 414-424 ◽  
Author(s):  
P. Kistler ◽  
Hs. Nitschmann

Parasitology ◽  
2008 ◽  
Vol 135 (10) ◽  
pp. 1151-1156 ◽  
Author(s):  
J. von OETTINGEN ◽  
M. NATH-CHOWDHURY ◽  
B. J. WARD ◽  
A. C. RODLOFF ◽  
M. J. ARROWOOD ◽  
...  

SUMMARYTo date, large-scale production ofCryptosporidium parvumoocysts has only been achieved by amplification in neonatal calves and sheep. Many laboratories currently depend on supplies from external sources and store oocysts for prolonged periods which results in progressive loss of viability. Six to 8-week-old interferon γ receptor knockout (IFNγR-KO) mice on a C57BL/6 background were inoculated by gavage (2000 oocysts/animal). Fecal pellets were collected daily from 7 days post-infection (p.i.) up to 2 weeks p.i. Intestinal oocyst yield was assessed at days 11, 12 and 14 p.i. by homogenization of intestinal tissues. Ether extraction and one or more NaCl flotations were used to purify oocysts. Total recoveries averaged 2·6×106oocysts/mouse from fecal material and 3·8×107oocysts/mouse from intestinal tissues. Overall, 2·3×109purified oocysts were obtained from 60 mice. Recovered oocysts were capable of sporulation and were shown to be infectious bothin vitroandin vivo. Oocyst amplification was achieved in only 11–14 days with minimal expense. The simplicity of this method presents a practical alternative for the routine passage, maintenance and storage ofC. parvumin biomedical laboratories.


Vox Sanguinis ◽  
1962 ◽  
Vol 7 (4) ◽  
pp. 414-424 ◽  
Author(s):  
P. Kistler ◽  
Hs. Nitschmann

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