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Nor binaltorphimine dihydrochloride nor bni

Manufactured by Abcam
Sourced in United Kingdom, United States

Nor-binaltorphimine dihydrochloride (nor-BNI) is a selective kappa opioid receptor antagonist. It is used in research applications.

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2 protocols using nor binaltorphimine dihydrochloride nor bni

1

Dynorphin A Neutralizing Antibody Protocol

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BAA and minocycline were purchased from Zelang Bio-Pharmaceutical (Nanjing, China) and Northeast Pharmaceuticals Group (Shenyang, China). Nor-binaltorphimine dihydrochloride (nor-BNI) and 5′-Guanidinonaltrindole (5′-GNTI) were obtained from Abcam (Cambridge, United Kingdom) and Sigma-Aldrich (St. Louis, MO, USA). dynorphin A (1−17) with peptide sequences of YGGFLRRIRPKLKWDNQ was synthesized by Dan Gang Peptides Co. (Hangzhou, China) with purity not less than 98%. The rabbit polyclonal antibodies neutralizing dynorphin A were purchased from Phoenix Pharmaceuticals (Burlingame, CA, USA), with specificity to dynorphin A (100%), but not to dynorphin B (0%), β-endorphin (0%), α-neo-endorphin (0%), or leu-enkephalin (0%) according to the manufacturer’s descriptions. Its specificity was also validated by the antigen absorption test from other laboratories (Wakabayashi et al., 2010 (link); Yamada et al., 2013 (link)). All of the reagents and drugs were diluted or dissolved in 0.9% normal saline or artificial cerebrospinal fluid (ACSF).
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2

Opioid and Sigma Receptor Antagonist Study

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Drugs used were as follows: (±)-N-allylnormetazocine hydrochloride, (+)-N-allylnormetazocine hydrochloride, (−)-N-allylnormetazocine hydrochloride (Sigma-Aldrich, St. Louis, MO, USA); 4-methoxy-3-(2-phenylethoxy)-N,N-dipropylbenzeneethanamine hydrochloride (NE-100), trans-(–)-3,4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide hydrochloride ((–)-U-50,488H; Tocris, Minneapolis, MO, USA); and nor-binaltorphimine dihydrochloride (nor-BNI; Abcam Biochemicals, Cambridge, MA, USA). Drug doses are expressed as the salt form. All drugs were dissolved in sterile water. NE-100 was administered by the intraperitoneal route; all other drugs were administered subcutaneously. The injection volume was 5 ml/kg.
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