Clia Kits

Improvement of in situ Follicular Activation and Early Development in Cryopreserved Human Ovarian Cortical Tissue by Co-Culturing with Mesenchymal Stem Cells.

Improvement of in situ Follicular Activation and Early Development in Cryopreserved Human Ovarian Cortical Tissue by Co-Culturing with Mesenchymal Stem Cells.

Follicle losses and network degeneration are major challenges in the ovarian tissue culture system. Mesenchymal (MSC) stem cells emit the cocktail of growth and cytokines that support adjacent cells
N-acetyltransferase 2 acetylator genotype-dependent N-acetylation of 4-aminobiphenyl in cryopreserved human hepatocytes.

N-acetyltransferase 2 acetylator genotype-dependent N-acetylation of 4-aminobiphenyl in cryopreserved human hepatocytes.

Arylamine N-Acetyltransferase is an xenobiotic metabolic enzyme responsible for detoxification of many drugs and carcinogens. Two n-acetyltransferase proteins (NAT1 and NAT2) are expressed in humans
The level of disbursement of iliaca artery of the human kriopreserved allografts (CHIAA) directly affects the fatigue of structural changes that occur during this process.

The level of disbursement of iliaca artery of the human kriopreserved allografts (CHIAA) directly affects the fatigue of structural changes that occur during this process.

Experiments were carried out at ten Chiaa. 10% dimethylsulphoxide in hydroxyethyl 6% starch solution is used as cryoprotectant; All Chiaa is cooled at a level controlled and stored in the liquid
Cryopreserved human oocytes and cord blood cells can produce macar stem cells somatic blood cells parent cells with hla homozygous type

Cryopreserved human oocytes and cord blood cells can produce macar stem cells somatic blood cells parent cells with hla homozygous type

Human pluripotent stem cells (PSC) through somatic cell nuclear transfer (SCNT) may be an important source for regenerative treatment. Low derivation efficiency of stem cells and human oocyte
Comparison of different thawing protocols in human cryopreserved venous grafts.

Comparison of different thawing protocols in human cryopreserved venous grafts.

The purpose of our study is to assess the impact of different disbursement protocols in morphological changes that arise in the grafting of cryopreserved human saphenous veins. This study was