産品簡介:
Bafilomycin A1 巴佛洛黴素A1
産品标簽
Bafilomycin A1巴佛洛黴素A1;Vacuolar H+ ATPase (V-ATPase) 液泡型ATP合成酶;Endosomal Acidification Inhibitor 胞内體酸化抑制劑;Autophagy Inhibitor 自(zì)吞噬;CAS NO:88899-55-2;
産品信息
産品名稱
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産品編号
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CAS NO.
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規格
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價格(元)
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Bafilomycin A1 巴佛洛黴素A1
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MZ8005-25UG
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88899-55-2
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25μg
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500
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Bafilomycin A1 巴佛洛黴素A1
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MZ8005-500UG
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88899-55-2
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500μg
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1450
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Bafilomycin A1 巴佛洛黴素A1
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MZ8005-1MG
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88899-55-2
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1mg
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2750
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産品描述
巴佛洛黴素A1(Bafilomycin A1),也稱為(wèi)NSC 381866,來源于灰色鏈黴菌(Streptomyces griseus)的一(yī)種
大環内酯類抗生(shēng)素。巴佛洛黴素A1是一(yī)種強效、選擇性的液泡型ATP合成酶(V-ATPase)抑制劑,在哺乳動物(wù)、植物(wù)或真菌細胞内阻斷這些質子泵活性,IC50在4-400nM範圍内。對大多(duō)數其他ATPase的抑制活性至少弱1000倍。Bafilomycin A1是一(yī)種知名的自(zì)吞噬晚期抑制劑,通(tōng)過抑制自(zì)吞噬體和溶酶體之間的融合來阻止自(zì)體吞噬泡的成熟。Bafilomycin A1能(néng)防止巨噬細胞溶酶體内的膽固醇轉運,并且用來區分不同類型ATPase。Bafilomycin A1還(hái)能(néng)抑制巨吞噬和促進結腸癌細胞凋亡發生(shēng)。
産品特性
1) CAS NO:88899-55-2
2) 化學名:(3Z,5E,7R,8S,9S,11E,13E,15S,16R)-8-Hydroxy-16-[(1S,2R,3S)-2-hydroxy-1-methyl-3-[(2R,4R, 5S,6R)-tetrahydro-2,4-dihydroxy-5-methyl-6-(1-methylethyl)-2H-pyran-2-yl]butyl]-3,15-dimethoxy-5,7,9,11- tetramethyloxacyclohexadeca-3,5,11,13-tetraen-2-one
3) 同義名:NSC 381866
4) 分子式:C35H58O9
5) 分子量:622.83
6) 純度:>95%(HPLC)
7) 外觀:黃色結晶粉末
8) 溶解性:溶于DMSO(0.1mg/ml),無水(shuǐ)乙醇(0.1mg/ml),甲醇,幾乎不溶于水(shuǐ)
9) 化學結構圖:
保存與運輸方法
保存:-20℃幹燥保存,3年(nián)有效。
運輸:冰袋運輸。
注意事(shì)項
1) 關于化合物(wù)溶解性:産品特性内的“≥”表明溶于标示濃度,但飽和溶解度未知。不同批次化合物(wù)的溶解度會(huì)有差異。
2) 為(wèi)了讓化合物(wù)更好的溶解,可通(tōng)過37℃加熱或(和)超聲波水(shuǐ)浴中震動片刻來處理。若實驗所需濃度過大甚至達産品溶解極限,請添加助溶劑助溶或自(zì)行調整濃度。
3) 為(wèi)了您的安全和健康,請穿實驗服并戴一(yī)次性手套操作。
儲存液制備
質量
溶劑體積
濃度
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25µg
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500µg
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1mg
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1mM
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40.1394 µL
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0.8027 mL
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1.6056 mL
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5mM
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8.0279 µL
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0.1605 mL
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0.3211 mL
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【溫馨提示】:請根據産品在不同溶劑中的溶解度選擇合适的溶劑配制儲備液;一(yī)旦配成溶液,請分裝保存,避免反複凍融造成的産品失效。儲備液置于-80°C保存,約6個(gè)月(yuè)有效;-20°C保存,約1個(gè)月(yuè)有效。溶液儲存的過程中避免強光(guāng)直射。
使用方法【源自(zì)文獻,僅作參考】
文獻1,Yasuo Hayashi, et al.(2006) Effects of bafilomycin A1, a vacuolar type H+ ATPase inhibitor, on the thermosensitivity of a human pancreatic cancer cell line, International Journal of Hyperthermia, 22:4, 275-285
體外研究(細胞水(shuǐ)平):
細胞類型(Cell Type):AsPC-1 cells
配制方法(Formulation):Bafilomycin A1 was dissolved in DMSO and then diluted to appropriate concentrations with the culture medium. The final concentration of DMSO in the medium was 1% or less.
實驗方法(Assay):The thermosensitizing effect of bafilomycin A1 and EIPA on AsPC-1 cells was quantified using a MTT colorimetric assay. 100μl cell suspension (1×105 cells/ml) was added to each well of a 96-well plate and incubated for 72 h at 37℃. The culture medium was then removed and 100 ml of pH 6.8 or 7.4 HEPES- buffered RPMI 1640 medium containing 1 mM bafilomycin A1 and/or 10 mM EIPA were added to each well. The plates were capped tightly and immersed in a 37C or 44C water bath for varying lengths of time. MTT assay was done to detect cell viability.
體内研究(動物(wù)模型):
動物(wù)模型(Animal Model):BALB/cA nude mice (Jcl-nu)
配制方法(Formulation):For in vivo studies, Bafilomycin A1 was dissolved in ethanol and then diluted to appropriate concentrations with PBS. The final concentration of ethanol in the medium was 1% or less.
實驗方法(Assay):AsPC-1 cells were injected s.c. into the right thigh of 6-week-old male mice. When tumors grew to ~150 mm3, they were divided randomly into eight experimental groups: a control group, a bafilomycin A1 (1.0 mg kg-1) treated group, a EIPA (3.0 mg kg-1 ) treated group, a bafilomycin A1 (1.0 mg kg-1) and EIPA (3.0 mg kg-1) treated group, a heated-only group, a heated group treated with bafilomycin A1 (1.0 mg kg-1), a heated group treated with EIPA (3.0 mg kg-1), a heated group treated with bafilomycin A1 (1.0 mg kg-1) and EIPA (3.0 mg kg-1). The non-heated groups received i.p. injections of 1.0mg kg-1 of bafilomycin A1 and/or 3.0 mg kg-1 of EIPA or PBS. The heated groups were injected IP with the drugs and tumours were heated beginning 60 min.
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— —Written/Edited by V. Shallan【版權歸MKBio懋康所有】
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