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Rat human crf

Manufactured by Merck Group
Sourced in United States

The Rat/human CRF is a lab equipment product developed by Merck Group. It is designed to detect and measure the levels of corticotropin-releasing factor (CRF) in rat and human samples. CRF is a neuropeptide that plays a crucial role in the body's stress response system. The Rat/human CRF product provides a reliable and accurate tool for researchers to study the function and regulation of CRF in various biological processes.

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3 protocols using rat human crf

1

Pharmacological Modulation of CRF Receptors

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The following drugs were used: rat/human CRF (Sigma-Aldrich, St. Louis, MO); CRF-R1 agonist stressin I and CRF-R1 antagonist NBI 27914 (Bio-Techne GmbH, Wiesbaden-Nordenstadt, Germany); CRF-R2 agonist urocortin-2 (Ucn-2), CRF-R2 antagonist K41498 (Bio-Techne GmbH, Wiesbaden-Nordenstadt, Germany); naloxone hydrochloride (Sigma-Aldrich, St. Louis, MO). Doses were calculated as the free base and drugs were dissolved in isotonic saline as vehicle. The volume of i.c.v. drug administration was 10 µl. For each dose a separate group of animals (n = 6) was used. Drugs were administered under brief isoflurane anesthesia.
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2

Pharmacological Modulation of CRF Receptors

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The following drugs were used: rat/human CRF (Sigma-Aldrich, St. Louis, MO, USA); CRF-R2 agonist urocortin-2 (Ucn-2), CRF-R2 antagonist K41498; CRF-R1 antagonist NBI35965 (Bio-Techne GmbH, Wiesbaden-Nordenstadt, Germany). Doses were calculated as the free base and drugs were dissolved in isotonic saline as vehicle. For each dose a separate group of animals (n = 6) was used. Drugs were administered during brief isoflurane anesthesia.
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3

Pharmacological Modulation of CRF Receptors

Check if the same lab product or an alternative is used in the 5 most similar protocols
The following drugs were used: rat/human CRF (Sigma-Aldrich, St. Louis, MO, USA); CRF-R2 agonist urocortin-2 (Ucn-2), CRF-R2 antagonist K41498; CRF-R1 antagonist NBI35965 (Bio-Techne GmbH, Wiesbaden-Nordenstadt, Germany). Doses were calculated as the free base and drugs were dissolved in isotonic saline as vehicle. For each dose a separate group of animals (n = 6) was used. Drugs were administered during brief isoflurane anesthesia.
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