Literature DB >> 6684810

An improved method for chromosome preparations from preimplantation mammalian embryos, oocytes or isolated blastomeres.

A P Dyban.   

Abstract

A method is described for making chromosome preparation from mammalian oocytes or preimplantation embryo, with or without the zona pellucida, or from isolated blastomeres. It is more robust and requires less skill and experience than previous techniques, yet chromosome structure is well preserved and very high quality preparations can be made. The method, which involves use of cold hypotonic solution and very cold fixative, reduces turbulence and allows even single blastomeres to be located and handled with relative case, while the duration of hypotonic treatment becomes noncritical. The softening solution recommended contains no lactic acid and hence does not harm the chromosomes.

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Year:  1983        PMID: 6684810     DOI: 10.3109/10520298309066756

Source DB:  PubMed          Journal:  Stain Technol        ISSN: 0038-9153


  13 in total

1.  A simple method for counting nuclei in the preimplantation mouse embryo.

Authors:  K M Ebert; R E Hammer; V E Papaioannou
Journal:  Experientia       Date:  1985-09-15

2.  Visualization and cytogenetic analysis of second polar body chromosomes following its fusion with a one-cell mouse embryo.

Authors:  Y Verlinsky; D Dozortsev; S Evsikov
Journal:  J Assist Reprod Genet       Date:  1994-03       Impact factor: 3.412

3.  Chromosome analysis of single- and multipronucleated human zygotes proceeded after the intracytoplasmic sperm injection procedure.

Authors:  E Macas; B Imthurn; M Roselli; P J Keller
Journal:  J Assist Reprod Genet       Date:  1996-04       Impact factor: 3.412

4.  Blastomere karyotyping and transfer of chromosomally selected embryos. Implications for the production of specific animal models and human prenatal diagnosis.

Authors:  C Bacchus; W Buselmaier
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

5.  Cytogenetic analysis of human oocytes parthenogenetically activated by puromycin.

Authors:  P De Sutter; D Dozortsev; P Vrijens; R Desmet; M Dhont
Journal:  J Assist Reprod Genet       Date:  1994-09       Impact factor: 3.412

6.  Effect of intracellular Ca2+ chelation with the acetoxymethyl ester-derived form of bis(o-aminophenoxy)ethane-N,N,N,N',N'-tetraacetic acid on meiotic division and chromosomal segregation in mouse oocytes.

Authors:  F J Vendrell; J Ten; M N De Oliveira; A Cano; J J Tarin
Journal:  J Assist Reprod Genet       Date:  1999-05       Impact factor: 3.412

7.  Complex cytogenetic analysis of early lethality mouse embryos.

Authors:  Qi Tian; Amy E Hanlon Newell; Yingming Wang; Susan B Olson; Lev M Fedorov
Journal:  Chromosome Res       Date:  2011-04-20       Impact factor: 5.239

8.  Development, Characterization, and Pluripotency Analysis of Buffalo (Bubalus bubalis) Embryonic Stem Cell Lines Derived from In Vitro-Fertilized, Hand-Guided Cloned, and Parthenogenetic Embryos.

Authors:  Syed Mohmad Shah; Neha Saini; Syma Ashraf; Mohammad Zandi; Radhey Sham Manik; Suresh Kumar Singla; Prabhat Palta; Manmohan Singh Chauhan
Journal:  Cell Reprogram       Date:  2015-07-13       Impact factor: 1.987

9.  Parthenogenetic activation of human oocytes by puromycin.

Authors:  P De Sutter; D Dozortsev; J Cieslak; G Wolf; Y Verlinsky; A Dyban
Journal:  J Assist Reprod Genet       Date:  1992-08       Impact factor: 3.412

10.  Visualization of second polar body chromosomes in fertilized and artificially activated mouse oocytes treated with okadaic acid.

Authors:  A P Dyban; P De Sutter; D Dozortsev; Y Verlinsky
Journal:  J Assist Reprod Genet       Date:  1992-12       Impact factor: 3.412

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