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  1. Cell Cycle/DNA Damage Apoptosis Anti-infection Metabolic Enzyme/Protease NF-κB Immunology/Inflammation
  2. Topoisomerase Apoptosis Antibiotic Bacterial Mitochondrial Metabolism Reactive Oxygen Species
  3. Ciprofloxacin

Ciprofloxacin  (Synonyms: 環(huán)丙沙星; Bay-09867)

目錄號(hào): HY-B0356 純度: 99.94%
COA 產(chǎn)品使用指南 技術(shù)支持

Ciprofloxacin (Bay-09867) 是一種口服有效的拓?fù)洚悩?gòu)酶 IV 抑制劑。Ciprofloxacin 誘導(dǎo)線粒體 DNA 和核 DNA 損傷并導(dǎo)致線粒體功能障礙和活性氧產(chǎn)生。Ciprofloxacin 具有抗增殖活性并誘導(dǎo)細(xì)胞凋亡 (apoptosis)。Ciprofloxacin 是一種氟喹諾酮類抗生素,具有強(qiáng)大的抗菌活性。

MCE 的所有產(chǎn)品僅用作科學(xué)研究或藥證申報(bào),我們不為任何個(gè)人用途提供產(chǎn)品和服務(wù)

Ciprofloxacin Chemical Structure

Ciprofloxacin Chemical Structure

CAS No. : 85721-33-1

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  • 生物活性

  • 純度 & 產(chǎn)品資料

  • 參考文獻(xiàn)

生物活性

Ciprofloxacin (Bay-09867) is a potent, orally active topoisomerase IV inhibitor. Ciprofloxacin induces mitochondrial DNA and nuclear DNA damage and lead to mitochondrial dysfunction, ROS production. Ciprofloxacin has anti-proliferative activity and induces apoptosis. Ciprofloxacin is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity[1][2][3][4].

IC50 & Target

Quinolone

 

體外研究
(In Vitro)

Ciprofloxacin (Bay-09867) (5-50 μg/mL;0-24 小時(shí);肌腱細(xì)胞) 抑制細(xì)胞增殖并導(dǎo)致細(xì)胞周期停滯在 G2/M 期[1]。
Ciprofloxacin (Bay-09867) 對(duì)鼠疫桿菌和炭疽桿菌表現(xiàn)出強(qiáng)效活性,MIC90 分別為 0.03 μg/mL 和 0.12 μg/mL[2]。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cycle Analysis[1]

Cell Line: Tendon cells
Concentration: 5, 10, 20 and 50 μg/mL
Incubation Time: 24 hours
Result: Decreased the cellularity of tendon cells.

Apoptosis Analysis[1]

Cell Line: Tendon cells
Concentration: 50 μg/mL
Incubation Time: 24 hours
Result: Arrested cell cycle at the G2/M phase and inhibited cell division in tendon cells.

Western Blot Analysis[1]

Cell Line: Tendon cells
Concentration: 50 μg/mL
Incubation Time: 0, 6, 12, 17 and 24 hours
Result: Down-regulated the expression of CDK-1 and cyclin B protein and mRNA. Up-regulated the expression of PLK-1 protein.
體內(nèi)研究
(In Vivo)

Ciprofloxacin(Bay-09867)(30 mg/kg;腹腔注射;持續(xù) 24 小時(shí);BALB/c 小鼠)在小鼠肺鼠疫模型中具有預(yù)防鼠疫耶爾森菌的作用[3]。
Ciprofloxacin(Bay-09867)(100 mg/kg;ig;每日,持續(xù) 4 周;C57BL/6J 小鼠)通過降低 LOX 水平并增加主動(dòng)脈壁中 MMP 水平和活性來加速主動(dòng)脈根部擴(kuò)張并增加主動(dòng)脈夾層和破裂的發(fā)生率[4]。
Ciprofloxacin(Bay-09867)(100 mg/kg;ig;每日一次,持續(xù) 4 周;C57BL/6J 小鼠)可誘導(dǎo) DNA 損傷和 DNA 釋放到細(xì)胞質(zhì)、線粒體功能障礙以及激活細(xì)胞質(zhì) DNA 傳感器信號(hào)。乳酸環(huán)丙沙星可增加主動(dòng)脈壁的細(xì)胞凋亡和壞死性凋亡[4]。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: BALB/c mice[3]
Dosage: 30 mg/kg
Administration: Intraperitoneal injection; for 24 hours
Result: Reduced the lung bacterial load in murine model of pneumonic plague.
Animal Model: C57BL/6J mice[4]
Dosage: 100 mg/kg
Administration: Oral gavage; daily, for 4 weeks
Result: Had aortic destruction that was accompanied by decreased LOX expression and increased MMP expression and activity.
Animal Model: C57BL/6J mice[4]
Dosage: 100 mg/kg
Administration: Oral gavage; daily, for 4 weeks
Result: Caused mitochondrial DNA and nuclear DNA damage, leading to mitochondrial dysfunction and ROS production. Increased apoptosis and necroptosis in the aortic wall.
Clinical Trial
分子量

331.34

Formula

C17H18FN3O3

CAS 號(hào)
性狀

固體

顏色

White to off-white

中文名稱

環(huán)丙沙星

運(yùn)輸條件

Room temperature in continental US; may vary elsewhere.

儲(chǔ)存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性數(shù)據(jù)
細(xì)胞實(shí)驗(yàn): 

0.1 M HCL 中的溶解度 : 16.67 mg/mL (50.31 mM; ultrasonic and warming and adjust pH to 2 with HCl and heat to 60°C)

H2O 中的溶解度 : 6.78 mg/mL (20.46 mM; ultrasonic and warming and adjust pH to 3 with 1 M HCL and heat to 60°C)

DMSO 中的溶解度 : 4.86 mg/mL (14.67 mM; ultrasonic and warming and adjust pH to 5 with 1 M HCL and heat to 60°C; 吸濕的 DMSO 對(duì)產(chǎn)品的溶解度有顯著影響,請(qǐng)使用新開封的 DMSO)

配制儲(chǔ)備液
濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg
1 mM 3.0180 mL 15.0902 mL 30.1805 mL
5 mM 0.6036 mL 3.0180 mL 6.0361 mL
查看完整儲(chǔ)備液配制表

* 請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液;一旦配成溶液,請(qǐng)分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效
儲(chǔ)備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C儲(chǔ)存時(shí),請(qǐng)?jiān)?個(gè)月內(nèi)使用,-20°C儲(chǔ)存時(shí),請(qǐng)?jiān)?個(gè)月內(nèi)使用。

* 備注:如您選擇水作為儲(chǔ)備液,請(qǐng)稀釋至工作液后,再用 0.22 μm 的濾膜過濾除菌后使用。

  • 摩爾計(jì)算器

  • 稀釋計(jì)算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

質(zhì)量
=
濃度
×
體積
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

濃度 (start)

C1

×
體積 (start)

V1

=
濃度 (final)

C2

×
體積 (final)

V2

動(dòng)物溶解方案計(jì)算器
請(qǐng)輸入動(dòng)物實(shí)驗(yàn)的基本信息:

給藥劑量

mg/kg

動(dòng)物的平均體重

g

每只動(dòng)物的給藥體積

μL

動(dòng)物數(shù)量

由于實(shí)驗(yàn)過程有損耗,建議您多配一只動(dòng)物的量
計(jì)算結(jié)果
工作液所需濃度 : mg/mL
純度 & 產(chǎn)品資料
參考文獻(xiàn)

完整儲(chǔ)備液配制表

* 請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液;一旦配成溶液,請(qǐng)分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效。
儲(chǔ)備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C儲(chǔ)存時(shí),請(qǐng)?jiān)?個(gè)月內(nèi)使用,-20°C儲(chǔ)存時(shí),請(qǐng)?jiān)?個(gè)月內(nèi)使用。

可選溶劑 濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg 25 mg
DMSO / H2O / 0.1 M HCL 1 mM 3.0180 mL 15.0902 mL 30.1805 mL 75.4512 mL
5 mM 0.6036 mL 3.0180 mL 6.0361 mL 15.0902 mL
10 mM 0.3018 mL 1.5090 mL 3.0180 mL 7.5451 mL
H2O / 0.1 M HCL 15 mM 0.2012 mL 1.0060 mL 2.0120 mL 5.0301 mL
20 mM 0.1509 mL 0.7545 mL 1.5090 mL 3.7726 mL
0.1 M HCL 25 mM 0.1207 mL 0.6036 mL 1.2072 mL 3.0180 mL
30 mM 0.1006 mL 0.5030 mL 1.0060 mL 2.5150 mL
40 mM 0.0755 mL 0.3773 mL 0.7545 mL 1.8863 mL
50 mM 0.0604 mL 0.3018 mL 0.6036 mL 1.5090 mL

* 備注:如您選擇水作為儲(chǔ)備液,請(qǐng)稀釋至工作液后,再用 0.22 μm 的濾膜過濾除菌后使用。

Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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