PRIMARY HUMAN BRAIN CELLS

FROM CELL SYSTEMS

AnaBios is Your Source for High-Quality Human Hepatocytes

AnaBios primary human hepatocytes provide the most comprehensive metabolic activity for researchers studying liver function and drug metabolism. Our hepatocytes are carefully isolated and characterized to ensure excellent quality and consistency. AnaBios hepatocytes have demonstrated high viability and functionality, making them an ideal model for predicting drug metabolism and toxicity in humans. 

 

  • Our tiered qualification process involves multiple stages of testing to ensure superior quality and consistency of hepatocytes across multiple lots.
  • Large hepatocyte lot sizes enable researchers to perform experiments with the same batch of cells for extended periods, reducing experimental variability.
  • Our high cell viability allows for more accurate and reliable prediction of drug metabolism and toxicity in the human liver.
  • Extensive donor information provides researchers with a deeper understanding of the variability in drug metabolism and toxicity responses across different patient populations, enabling the development of more personalized medicine 
  • AnaBios offers fast, reliable shipping for domestic and international orders.

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AnaBios Hepatocyte Medium Kit is a specialized solution designed to facilitate the safe and efficient thawing process of cryopreserved hepatocytes.


Citations


Blast-Induced Injury Responsive Relative Gene Expression of Traumatic Brain Injury Biomarkers in Human Brain Microvascular Endothelial Cells

The study investigates blood-brain barrier (BBB) disruption in traumatic brain injury (TBI) by examining the gene expression of TBI biomarkers and neuronal function-related factors in human brain microvascular cells (HBMVECs) using an in-vitro blast TBI model. The results show significant changes in gene expression in response to TBI, depending on injury intensity and time after injury. This suggests that understanding HBMVEC cell signaling could be crucial in comprehending the interaction between the BBB and TBI pathophysiology, warranting further investigation.

 


Blast-Induced Injury Responsive Relative Gene Expression of Traumatic Brain Injury Biomarkers in Human Brain Microvascular Endothelial Cells

The study investigates blood-brain barrier (BBB) disruption in traumatic brain injury (TBI) by examining the gene expression of TBI biomarkers and neuronal function-related factors in human brain microvascular cells (HBMVECs) using an in-vitro blast TBI model. The results show significant changes in gene expression in response to TBI, depending on injury intensity and time after injury. This suggests that understanding HBMVEC cell signaling could be crucial in comprehending the interaction between the BBB and TBI pathophysiology, warranting further investigation.

 


Blast-Induced Injury Responsive Relative Gene Expression of Traumatic Brain Injury Biomarkers in Human Brain Microvascular Endothelial Cells

The study investigates blood-brain barrier (BBB) disruption in traumatic brain injury (TBI) by examining the gene expression of TBI biomarkers and neuronal function-related factors in human brain microvascular cells (HBMVECs) using an in-vitro blast TBI model. The results show significant changes in gene expression in response to TBI, depending on injury intensity and time after injury. This suggests that understanding HBMVEC cell signaling could be crucial in comprehending the interaction between the BBB and TBI pathophysiology, warranting further investigation.

 

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