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Clawson Stainless Chemical High material Sealed Fluid Storage Pressurize Vesse San Antonio Mall

Clawson Stainless Chemical Sealed Pressurize Fluid Storage Vesse

$244

Clawson Stainless Chemical Sealed Pressurize Fluid Storage Vesse

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Item specifics

Condition:
Used:
An item that has been used previously. The item may have some signs of cosmetic wear, but is fully operational and functions as intended. This item may be a floor model or store return that has been used. See the seller’s listing for full details and description of any imperfections.
Seller Notes:
“Excess inventory. In as pictured condition, Cosmetic wear and tear, please review an actual pic.”
Brand:
Clawson
Model:
Container
MPN:
345GL
UPC:
Does Not Apply







Clawson Stainless Chemical Sealed Pressurize Fluid Storage Vesse

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Gut is a leading international journal in gastroenterology and hepatology and has an established reputation for publishing first class clinical research of the alimentary tract, the liver, biliary tree and pancreas. Gut delivers up-to-date, authoritative, clinically oriented coverage in all areas of gastroenterology and hepatology. Regular features include articles by leading authorities describing novel mechanisms of disease and new management strategies, both diagnostic and therapeutic, likely to impact on clinical practice within the foreseeable future.

Gut is an official journal of the British Society of Gastroenterology and has two companion titles, Frontline Gastroenterology for education and practice and BMJ Open Gastroenterology for sound science clinical research.

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Our new online collection highlights all research relating to the COVID-19 pandemic published by Gut, Frontline Gastroenterology and BMJ Open Gastroenterology. It is updated regularly as new articles are published.

 

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Hepatitis C reference viruses highlight potent antibody responses and diverse viral functional interactions

To cite: Bankwitz D, Bahai A, Labuhn M, et al. Gut 2021;70:1734-1745.

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Objective: Neutralising antibodies are key effectors of infection-induced and vaccine-induced immunity. Quantification of antibodies’ breadth and potency is critical for understanding the mechanisms of protection and for prioritisation of vaccines. Here, we used a unique collection of human specimens and HCV strains to develop HCV reference viruses for quantification of neutralising antibodies, and to investigate viral functional diversity.

Conclusions: Representative isolates from six neutralisation clusters broadly reconstruct the functional HCV neutralisation space. They enable high resolution profiling of HCV neutralisation and they may reflect viral functional and antigenic properties important to consider in HCV vaccine design.

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