国产一级一级理论片一区二区_久久综合图区亚洲综合图区_国产精品V欧美精品av日韩_日韩精品成人在线_亚洲欧美日韩动漫_国产精品一二三区在线观看公司_日韩成人无码一区二区三区


免費(fèi)注冊(cè)快速求購(gòu)


分享
舉報(bào) 評(píng)價(jià)

tlyon000400 37360疼痛甩尾

參考價(jià)面議
具體成交價(jià)以合同協(xié)議為準(zhǔn)
  • 公司名稱 圖拉揚(yáng)科技
  • 品牌
  • 型號(hào) tlyon000400
  • 所在地
  • 廠商性質(zhì) 其他
  • 更新時(shí)間 2020/12/25 22:17:12
  • 訪問次數(shù) 238

該廠商其他產(chǎn)品

我也要出現(xiàn)在這里

測(cè)量大、小鼠尾巴部受紅外熱刺激的痛覺閾值

詳細(xì)信息 在線詢價(jià)

  • 產(chǎn)品名稱:37360疼痛甩尾
  • 訂貨號(hào):tlyon000400
  • 品牌名稱:意大利Ugo
如果您發(fā)現(xiàn)產(chǎn)品信息不準(zhǔn)確利用好,歡迎糾錯(cuò)深入各系統;或咨詢相關(guān)類別、品牌產(chǎn)品尤為突出,請(qǐng)

37360 - 疼痛甩尾

疼痛甩尾主要是用于測(cè)量大規定、小鼠尾巴部受紅外熱刺激的痛覺閾值。實(shí)驗(yàn)時(shí)空間載體,當(dāng)動(dòng)物感覺疼痛高質量,尾巴會(huì)輕敲臺(tái)面,內(nèi)置傳感器會(huì)立刻檢測(cè)到重要組成部分,停止計(jì)時(shí)和關(guān)閉光源流程,即儀器自動(dòng)記錄反應(yīng)時(shí)間和光源強(qiáng)度。數(shù)據(jù)可通過U盤勃勃生機、USB數(shù)據(jù)線等導(dǎo)出助力各業。

該儀器中有一可調(diào)強(qiáng)度的紅外光源,其紅外光主要是通過一拋物面反射鏡聚焦在實(shí)驗(yàn)動(dòng)物的尾巴上提供有力支撐。實(shí)驗(yàn)時(shí)應用,操作人員將實(shí)驗(yàn)動(dòng)物置于儀器上,把動(dòng)物的尾巴放在紅外光源處技術交流,接受刺激先進的解決方案。

該儀器也可以在小鼠上進(jìn)行實(shí)驗(yàn),有小鼠設(shè)備配件可供選擇創造更多。
延遲時(shí)間和強(qiáng)度能夠通過USB或者串行端口導(dǎo)出宣講活動。USB和軟件都包含在內(nèi)。

特征

優(yōu)點(diǎn)

儀器自動(dòng)記錄實(shí)驗(yàn)數(shù)據(jù)

精度高工藝技術,避免人為因素引起的誤差

包含U盤和軟件

可獨(dú)立工作效率,也可連接電腦使用

儀器工作臺(tái)表面無突出和遮擋物件

操作方便,實(shí)驗(yàn)重復(fù)性好

規(guī)格:

命令:

軟鍵和腳踏板

連接電腦:

DELTA 9-pin連接頭近年來,USB連線

數(shù)據(jù)讀戎v道理。?/p>

液晶顯示

電源:

universal mains 85-264 VAC, 50-60Hz

打印:

微型熱敏打印機(jī)(需另外購(gòu)買)

工作溫度:

15° - 30° C

開始:

紅外開關(guān)

聲級(jí):

< 70 dB

紅外強(qiáng)度:

10-99級(jí)間可調(diào)

紅外光源燈泡性能穩定;

Halogen "Bellaphot", Mod. 64607 OSRAM, 8V-50W

反應(yīng)時(shí)間:

液晶屏顯示全面革新,分辨率為0.1s

校準(zhǔn):

紅外熱輻射計(jì)(需另外購(gòu)買)

截止時(shí)間:

預(yù)置作用,15 - 60 s間

附件:

37360-325:

小鼠束縛器,25 mm I.D.

37360-330:

E-HR 002:

小鼠束縛器行業分類,30 mm I.D.

替換燈泡

37300

紅外熱輻射計(jì)

57145

微型打印機(jī)

參考文獻(xiàn)

方法

- F.E. D’Amour & D.L. Smith: "A Method for Determining Loss of Pain Sensation." J. Pharmacol. Exp. Therap. 72: 74-79, 1941.

涉及UB的甩尾實(shí)驗(yàn)

- T.O. Lilius et alia: "The Mineralocorticoid Receptor Antagonist Spironolactone Enhances Morphine Antinociception” Eur. J. of Pain online view, 2013

- J.W. Little et alia: “Spinal Mitochondrial-Derived Peroxynitrite Enhances Neuroimmune Activation During Morphine Hyperalgesia and Antinociceptive Tolerance” Pain 154 (7): 978-986, 2013

- P.J. McLaughlin et alia: “Behavioral Effects of the Novel Potent Cannabinoid CB1 Agonist AM 4054”Pharmacology Biochemistry and Behavior 109: 16-22, 2013

- T.A. Kosten et alia: “A Morphine Conjugate Vaccine Attenuates the Behavioral Effects of Morphine in Rats” Progr. in Neuro-Psychopharmacol. and Biol. Psychiatry 45: 223–229, 2013

- T.C. Chen et alia: “Spontaneous inflammatory Pain Model From a Mouse Line With N-ethyl-N-nitrosourea Mutagenesis” J. Biomed. Science 19 (55): 2–15, 2012

- J. Walsh et alia: “Disruption of Thermal Nociceptive Behaviour in Mice Mutant for the Schizophrenia-Associated Genes NRG1, COMT and DISC1” Brain Res. 1348: 114-119, 2012

- K. Guillemyn et alia: “In vivo Antinociception of Potent mu Opioid Agonist Tetrapeptide Analogues and Comparison with a Compact Opioid Agonist-neurokin 1 Receptor Antagonist Chimera” Molecular Brain5 (4): 2-11, 2012

- A.J. Morrison et alia: “Design, Synthesis, and Structure–Activity Relationships of indole-3-heterocycles as Agonists of the CB1 Receptor” Bioorganic & Medicinal Chemistry Letters 21: 506-509, 2011

- M. Spetea et alia: “In vitro and in vivo Pharmacological Profile of the 5-benzyl Analogue of 14-methoxymetopon, a Novel μ Opioid Analgesic with Reduced Propensity to Alter Motor Function” Eur. J. Pharmac. Sciences 41: 125-135, 2010

- C.A. Boehm et alia: “Midazolam Enhances the Analgesic Properties of Dexmedetomidine in the Rat”Vet. Anaesthesia and Analgesia 37 (6): 550-556, 2010

- M.A. Philips et alia: “Myg1-Deficient Mice Display Alterations in Stress-Induced Responses and Reduction of Sex-Dependent Behavioural Differences” Behav. Brain Res. 207: 182-195, 2010

- C. Dawson et alia: “ Dexmedetomidine Enhances Analgesic Action of Nitrous Oxide” Anesthesiology 100 (4): 894−904, 2004

- P. Tolu et alia: “ Effects of Long-Term Acetyl-L-carnitine Administation in Rats: I. Increased Dopamine Output in Mesocorticolimbic Areas and Protection Toward Acute Stress Exposure” Neuropsychopharmacol. 27 (3): 410-420, 2002

- R. Nadeson et alia: “ Potentiation by Ketamine of * Antinociception. I. An Experimental Study in Rats Showing that Ketamine Administered by Non-Spinal Routes Targets Spinal Cord Antinociceptive Systems” Br. J. Anaesthesia 88 (5): 685−691, 2002
- L. Jasmin et alia: “ The NK1 Receptor mediates Both the Hyperalgesia and the Resistance to Morphine in Mice Lacking Noradrenaline” PNAS 99 (2): 1029−1034, 2002
- G.L. Fraser et alia: “ Antihyperalgesic Effects of Opioid Agonists in a Rat Model of Chronic Inflammation” Br. J. Pharmacol. 129: 1668−1672, 2000
- M. Xu et alia: “ Effects of Radolmidine, a Novel α2- Adrenergic Agonist Compared with Dexmedetomidine in Different Pain Models in the Rat” Anesthesiology 93 (2): 473−481, 2000
- A. Köster et alia: “Targeted Disruption of the Orphanin Fq/Nociceptin Gene Increases Stress Susceptibility and Impairs Stress Adaptation In Mice” Neurobiology 96 (18): 10444-10449, 1999
- I. Sora et alia: “Opiate Receptor Knockout Mice Define µ Receptor Roles in Endogenous Nociceptive Responses and Morphine-Induced Analgesia” Neurobiology 94: 1544-1549, 1997
- C.T. Dourish et alia: "The Selective CCK-B Receptor Antagonist L-365,260 Enhances Morphine Analgesia and Prevents Morphine Tolerance in the Rat" Europ. J. Pharmacol. 176: 35-44, 1990
- P.W. Nance & J. Sawinok: "Substance P-Induced Long-Term Blockade of Spinal Adrenergic Analgesia: Reversal by Morphine and Naloxone" J. Pharmacol. Exp. Therap. Vol. 240, No. 3: 972-977, 1987


同類產(chǎn)品推薦


提示

×

*您想獲取產(chǎn)品的資料:

以上可多選體製,勾選其他構建,可自行輸入要求

個(gè)人信息:

仪征市| 宜都市| 广宗县| 横山县| 隆德县| 大足县| 文安县| 宜黄县| 达拉特旗| 韶山市| 温州市| 喀喇沁旗| 沧州市| 千阳县| 连城县| 青海省| 岢岚县| 陆良县| 高尔夫| 社旗县| 岚皋县| 合作市| 祁门县| 博罗县| 阳春市| 黄冈市| 吴旗县| 威海市| 淮南市| 门头沟区| 汝南县| 彭水| 平和县| 南昌县| 习水县| 扬州市| 山东省| 襄汾县| 喀什市| 凯里市| 东阳市|