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B Avery

Publications and source records attributed to B Avery.

46 records · Page 3Linked to original sources

Sex determination of bovine embryos based on embryonic cleavage rates.

Bovine embryos (n = 64) collected at day-6 from 10 superovulated and inseminated donors were evaluated upon recovery and again after incubation for approx. 12 hrs. According to cleavage rate they could be divided into a fast, an intermediate and a slow developing group, respectively. This grouping was correlated to embryonic sex determined by karyotyping (n = 29). From the fast developing group we found 7 males and 2 females (male ratios 78%), from the intermediate group 3 males and 8 females (male ratio 27%) and from the slow group 1 male and 8 females (male ratio 11%). From this preliminary study it is concluded that the rate of embryonic development may be used as a sex discriminator.

Animals↗

Sex determination of bovine embryos using H-Y antibodies.

6 days old bovine embryos (n = 126) were obtained from 8 superovulated cows or heifers by flushing the uteri and oviducts either non-surgically or after slaughter. Part of the embryos (n = 72) (morula stages) were placed in Ham's F-10 or PBS supplemented with 10% fetal calf serum (FCS) diluted 1:1 with supernatant from the H-Y antibody producing clone and cultured at 38 degrees C, in 5% CO2/95% air and 100% humidity. Control embryos (n = 54) were cultured in H-Y antibody free medium. After culture the embryos could be separated into a blastocyst--and a morula group. A subsequent colchemid and hypotonic treatment and fixation and Giemsa staining allowed a precise karyotyping, and thus sex determination for 36 H-Y antibody treated embryos and 22 control embryos. The limiting factor for proper karyotyping was lack of metaphases, incomplete methaphases or poor preparation. Among the H-Y antibody treated embryos we found 7 males and 15 females in the blastocyst and 14 males and 0 females in the morula group. A statistical analysis of these proportions led to the conclusion that the H-Y antibody had a significant influence on the sex ratio.

Animals↗

Serological analyses of different mink Aleutian disease virus strains.

Four different isolates of Aleutian disease virus have been compared electrophoretically and serologically. These were the DK and Utah 1 isolates, known as highly virulent strains, the Pullman isolate, known as a low virulent strain and the avirulent ADV-G isolate, which is the only strain grown in cell culture. ADV-G was shown to migrate in agarose electrophoresis 22 per cent slower than the other strains. Several murine monoclonal antibodies were prepared against each of the isolates. Each one reacted with all 4 of the isolates, but a few showed higher affinity for some of the isolates. Competitive RIA analyses were also performed, and these studies indicated some serological differences between the 4 strains. It is concluded that ADV-G polypeptides are chemically different but immunologically cross-reacting with the polypeptides present on the field ADV strains. It is suggested that the small serological differences seen between the field strains might be caused by slightly different in vivo proteolytic degradation of the viral capsid proteins and thus might not be taken as an indication of strain variation.

Aleutian Mink Disease Virus↗

An easy method for comparing antibody affinities to related antigens.

Four different Aleutian disease virus (ADV) isolates were coated to 1/4" polystyrene balls. The binding capacity of these balls against different mouse hybridoma antibodies prepared against each of the ADV isolates was investigated in two ways. The different ADV-coated balls were either mixed in a tube (competition between balls for antibody), or they were allowed to react separately with antibody (no competition). The difference in competitive and non-competitive binding values allows a comparison of antibody affinity against the four ADV isolates. Examples are given, where two hybridoma antibodies react better with the Danish isolate than with the three American isolates.

Aleutian Mink Disease Virus↗

Cytotoxicity of antisera to a myelogenous leukemia cell line with the Philadelphia chromosome.

Rabbit antisera to myelogenous leukemia (ML) cells were raised; ML cells from line K-562 that has the Philadelphia (Ph) chromosome were used as antigen. Antibodydependent, complement-mediated cytotoxicity was demonstrated by the trypan blue test and Cr release assay for cultured ML cells, whereas no cytotoxicity was demonstrated for cells from B (SB) and T (MOLT 4) lymphoblastoid cell lines. The antisera showed no cross-reactivity for normal human peripheral leukocytes or purified granulocytes. A low level (less than 8%) of cytotoxicity was directed against cell membrane associated fetal bovine serum proteins. Absorption of the immune serum with normal human bone marrow cells of first trimester human whole embryo cells reduced the cytotoxic titer to a similar extent; this suggested the possibility of crossreactivity between ML cells and fetal antigen(s). However, the ML antigen(s) was unrelated to carcinoembryonic antigen (CEA), since absorption with CEA had no effect on the serum cytotoxic titer. The anti-ML sera were cytotoxic for cells taken from 10 patients with chronic myelogenous leukemia and from 3 with acute myelogenous leukemia. In contrast, the leukocytes of 1 of 4 patients with acute lymphocytic leukemia, and 3 of 7 with chronic lymphocytic leukemia shared similar antigenic determinants as demonstrated by cytotoxicity tests. The significance of the cross-reactivity of some lymphatic and ML cells may be the result of the use of rabbit sera that did not distinguish antigens common to both granulocytic and lymphocytic cells, or it may reflect an "immature" or "blastic" antigen present on many leukemia cells.

Adult↗

A CEO roundtable on making mergers succeed.

The announcement in January of the merger between America Online and Time Warner marked the convergence of the two most important business trends of the last five years--the rise of the Internet and the resurgence of mergers and acquisitions. M&A activity is at a fever pitch, spurred in large part by the breathtaking influx of capital into the Internet space. And all signs indicate the trend will only accelerate. Against this background, an impressive group of experienced deal makers came together to share their experiences of what makes mergers work. They were assembled in Scottsdale, Arizona, under the auspices of the M&A Group, a professional society formed in 1999 for CEOs interested in M&A as a business strategy. Participants included top executives from Internet start-ups like Teligent; venture capital firms like Baroda Ventures; financial institutions like Merrill Lynch and PricewaterhouseCoopers; and major corporations like Allstate, Tyco International, SmithKline Beecham, Rohm and Haas, VF, Crown Cork & Seal, and Hughes Space and Communications. The spirited and surprisingly frank discussion cut a wide swath, considering issues such as whether most mergers fail to pan out as well as expected, how to increase the odds of success, the nuts and bolts of the integration process, the trade-offs between acquiring a company and growing from within, the importance of cultural issues, and why anyone would want to be on the board of a merged company.

Administrative Personnel↗