Anti ?Valerylfentanyl Carboxylic acid(戊酰芬太尼羧酸) mouse ?monoclonal ?antibody
應(yīng)用:Competitive Elisa:1:1000~5000?
產(chǎn)品名(Product Name)
Anti ?Valerylfentanyl Carboxylic acid(戊酰芬太尼羧酸) mouse monoclonal antibody
貨號(hào)(Catalog No.)
KL-10235Mo?
種類(Category)
Primary antibody
宿主(Host)
Mouse
反應(yīng)種屬(Species specificity)
CAS#: 117332-91-9
應(yīng)用實(shí)驗(yàn)(Tested applications)
Competitive Elisa
克隆性(Clonality)
Monoclonal
克隆編號(hào)(Clone No.)
95-F-6
偶連物(Conjugation)
Unconjugate
免疫原(Immunogen)
Valerylfentanyl Carboxylic acid
別名
Valeryl fentanyl (hydrochloride)
狀態(tài)(Form)
Liquid
儲(chǔ)存溶液(Buffer)
PBS, pH7.4, containing 0.05% proclin300, 50% glycerol.
存放條件(Storage)
Use a manual defrost freezer and avoid repeated freeze thaw cycles.
Store at 4 °C for frequent use.
Store at -20 to -80 °C for twelve months from the date of receipt.
濃度(Concentration)
1mg/ml
亞型(Isotype)
IgG1
純化方式(Purity)
Protein G purified from mice ascites
產(chǎn)品背景:Valerylfentanyl first appeared in toxicological assays in 2016 and through 2018, it has been reported in 6 countries worldwide, including North America, Europe, and Asia. It is being sold as heroin, an adulterant in
heroin, or as counterfeit pills. Few fatalities have been attributed to this substance although confiscations of drug containing valerylfentanyl appear to be increasing in some states in the U.S. Receptor binding data show that valerylfentanyl binds selectively to the mu subtype of opioid receptors with low nanomolar affinity relative to kappa and delta opioid receptors. Functional binding assays suggest that valerylfentanyl is a partial agonist at mu and kappa opioid receptors and an antagonist at delta receptors. However, in vivo pharmacology studies in rodents and non-human primates suggest that valerylfentanyl is a full mu agonist.No pharmacokinetic studies of valerylfentanyl are reported in the preclinical or clinical scientific literature.Valerylfentanyl appears to be less potent than other illicit mu agonists with a chemical structure that is similar to fentanyl. As such, its pharmacology and toxic effects are likely to be similar to fentanyl. It currently has no legitimate medical or veterinary uses and is relatively easy to manufacture. The totality of data currently available on valerylfentanyl suggests that it has high abuse potential and poses a serious public health threat?
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