TISCH 滤膜SF14528
TISCH 滤膜SF14528 1.0μm 47mm TISCH 滤膜SF14528 尼龙膜 100张/盒
TISCH 滤膜SF14528
尼龙膜
尺寸
孔径:1.0μm
直径:47mm
包装:100张/盒
TISCH 滤膜SF14528
尼龙膜
尺寸
孔径:1.0μm
直径:47mm
包装:100张/盒
荧光染料Dye Reagents GNF-2-PEG-acid;
GNF-2-PEG-acid 是GNF-2 的类似物,常被用作标记的化学或荧光探针。
GNF-2-PEG-acid Chemical Structure
规格 | 是否有货 | ||
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100 mg | ; | 询价 | ; |
250 mg | ; | 询价 | ; |
500 mg | ; | 询价 | ; |
* Please select Quantity before adding items.
生物活性 |
GNF-2-PEG-acid, an analogue of GNF-2, is usually used as a labeled chemical or fluorescent probe. |
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分子量 |
564.51 |
Formula |
C26H27F3N4O7 |
运输条件 |
Room temperature in continental US; may vary elsewhere. |
储存方式 |
Please store the product under the recommended conditions in the Certificate of Analysis. |
Munktell家具表面划痕耐油测试纸*Industrial Filter paper 1220
品牌:MUNKTELL 瑞典
型号:Grade1220
包装:1000片/包
直径:25mm
工业级
Munktell家具表面划痕耐油测试纸
*Industrial Filter paper 1220
品牌:MUNKTELL 瑞典
型号:Grade1220
包装:1000片/包
直径:25mm
工业级
Munktell 表面耐油性测试滤纸,主要用于以下用途:
1 对带划痕表面耐油脂性的评估(实木、木质基材)、测试描述带涂层的实木和木质基材表面耐刮擦性的测定方法,以及对带划痕的表面耐油脂性的评估方法。要求测试对象是成品家具/产品的表面,或是与成品家具/产品用相同处理和工艺过程的测试样。
2 表面对摩擦和油脂的抵抗性通过在磨损的区域用液体石蜡(油脂)评估抵抗性来测量带涂层的表面耐磨损至基材的抗性。此方法用于有高抵抗性要求的带涂层的木质表面,贴膜和薄片贴面。
此方法主要用于成品家具/产品,但也可用于两面与三个边缘暴露于水的并与家具/产品有相同表面处理的测试面板。 已经被宜家家居所有供应商zhi定测试滤纸。
Munktell家具表面划痕耐油测试纸
产品编号:
市场价:¥0.00元
会员价:¥0.00元
品牌:Oxford牛津
生产厂家:Oxford牛津
需求数量:
Oxford牛津1500系列PN90507小焦斑X光管
1500系列为无窗口X光管,专门为透视应用而设计。P/N 90507 型的特点是可提供非常小的等静焦斑,因而适用于高分辨应用领域特别是微型C臂透视设备。这种射线管配置了我们生产的独特的PF(Pin Flash)闪时吸气剂,因而保证了超高真空的长久性。它在两极操作模式下工作。
P/N 90507 | |
阳极电流 | 最大0.7毫安 |
阳极(靶)电压 | 最大80千伏 |
最大功率 | 56瓦连续 |
灯丝电压 | 2.25伏 @ 80千伏/0.7毫安 |
灯丝电流 | 1.7安培 |
稳定性 | 4小时内为0.2% |
焦斑大小 | 33微米 |
靶面角 | 20度 |
阴极类型 | 钨灯丝 |
尺寸 | 长3.39英寸,直径1.18英寸 |
重量 | 0.25磅(114克) |
天然产物 糖类和糖苷 Saccharides and Glycosides
L-Glucose (Synonyms: L-葡萄糖; L-(-)-Glucose) 纯度: ≥97.0%
L-Glucose (L-(-)-Glucose) 是 D-glucose 的一种对映体。L-Glucose 能促进食物的摄取。
L-Glucose Chemical Structure
CAS No. : 921-60-8
规格 | 价格 | 是否有货 | 数量 |
---|---|---|---|
10 mM * 1 mL in DMSO | ¥550 | In-stock | |
100 mg | ¥500 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
* Please select Quantity before adding items.
生物活性 |
L-Glucose (L-(-)-Glucose) is an enantiomer of D-glucose. L-Glucose can promote food intake[1]. |
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分子量 |
180.16 |
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Formula |
C6H12O6 |
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CAS 号 |
921-60-8 |
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中文名称 |
L-葡萄糖 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 60 mg/mL (333.04 mM; Need ultrasonic) 配制储备液
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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荧光染料Dye Reagents SPQ; 纯度: 99.97%
SPQ是被检测和测量膜离子传输机制的产品。
SPQ Chemical Structure
CAS No. : 83907-40-8
规格 | 价格 | 是否有货 | 数量 |
---|---|---|---|
Free Sample (0.1-0.5 mg) | ; | Apply now | ; |
10;mM;*;1 mL in Water | ¥880 | In-stock | |
50 mg | ¥800 | In-stock | |
100 mg | ¥1400 | In-stock | |
200 mg | ; | 询价 | ; |
500 mg | ; | 询价 | ; |
* Please select Quantity before adding items.
生物活性 |
SPQ is being used to examine and measure membrane chloride transport mechanisms. |
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分子量 |
281.33 |
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Formula |
C13H15NO4S |
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CAS 号 |
83907-40-8 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4deg;C, protect from light *In solvent : -80deg;C, 6 months; -20deg;C, 1 month (protect from light) |
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溶解性数据 |
In Vitro:;
H2O : 25 mg/mL (88.86 mM; Need ultrasonic) DMSO : < 1 mg/mL (insoluble or slightly soluble) 配制储备液
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Arnicolide D (Synonyms: 山金车内酯 D) 纯度: 99.20%
Arnicolide D 是一种从石胡荽 (Centipeda minima) 中分离出倍半萜内酯。Arnicolide D 调节细胞周期,激活 caspase 信号通路,并抑制 PI3K/AKT/mTOR 和 STAT3 信号通路。Arnicolide D 以剂量和时间依赖性方式显着抑制鼻咽癌 (NPC) 细胞生长。
Arnicolide D Chemical Structure
CAS No. : 34532-68-8
规格 | 价格 | 是否有货 | 数量 |
---|---|---|---|
1 mg | ¥1900 | In-stock | |
5 mg | ¥5710 | In-stock | |
10 mg | 询价 | ||
50 mg | 询价 |
* Please select Quantity before adding items.
生物活性 |
Arnicolide D is a sesquiterpene lactone isolated from Centipeda minima. Arnicolide D modulates the cell cycle, activates the caspase signaling pathway and inhibits the PI3K/AKT/mTOR and STAT3 signaling pathways. Arnicolide D inhibits Nasopharyngeal carcinoma (NPC) cell viability in a concentration- and time-dependent manner[1]. |
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IC50 & Target[1] |
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分子量 |
332.39 |
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Formula |
C19H24O5 |
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CAS 号 |
34532-68-8 |
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中文名称 |
山金车内酯 D |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) |
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参考文献 |
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PNPP disodium;(Synonyms: Para-nitrophenyl phosphate disodium) 纯度: 99.85%
PNPP (Para-nitrophenyl phosphate) disodium 是用于 ELISA 和常规分光光度测定的碱性和酸性磷酸酶的非蛋白质性显色底物。
PNPP disodium Chemical Structure
CAS No. : 4264-83-9
规格 | 价格 | 是否有货 | 数量 |
---|---|---|---|
Free Sample (0.1-0.5 mg) | ; | Apply now | ; |
10;mM;*;1 mL in Water | ¥500 | In-stock | |
500 mg | ¥350 | In-stock | |
1 g | ¥450 | In-stock | |
5 g | ¥800 | In-stock | |
10 g | ; | 询价 | ; |
50 g | ; | 询价 | ; |
* Please select Quantity before adding items.
生物活性 |
PNPP (Para-nitrophenyl phosphate) disodium is a non-proteinaceous chromogenic substrate for alkaline and acid phosphatases used in ELISA and conventional spectrophotometric assays. |
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体外研究 (In Vitro) |
Phosphatases catalyze the hydrolysis of PNPP liberating inorganic phosphate and the conjugate base of para-nitrophenol (pNP). The resulting phenolate is yellow, with a maximal absorption at 405 nm[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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分子量 |
263.05 |
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Formula |
C6H4NNa2O6P |
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CAS 号 |
4264-83-9 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4deg;C, sealed storage, away from moisture *In solvent : -80deg;C, 6 months; -20deg;C, 1 month (sealed storage, away from moisture) |
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溶解性数据 |
In Vitro:;
H2O : 160 mg/mL (608.25 mM; Need ultrasonic) 配制储备液
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |
Whatman定量滤纸-无灰级1443-110,Grade 43,圆片,110mm,100张/包。
LSKL, Inhibitor of Thrombospondin (TSP-1) (TFA);(Synonyms: LSKL, 血小板反应蛋白抑制剂 (TSP-1) 三氟醋酸盐) 纯度: 99.30%
LSKL, Inhibitor of Thrombospondin (TSP-1) TFA 是一种衍生自 LAP-TGFβ 的四肽,是一种竞争性的 TGF-β1 拮抗剂。LSKL, Inhibitor of Thrombospondin (TSP-1) TFA 抑制 TSP-1 与 LAP 的结合并减轻肾间质纤维化和肝纤维化。LSKL, Inhibitor of Thrombospondin (TSP-1) TFA 通过抑制 TSP-1 介导的 TGF-β1 活性来抑制蛛网膜下纤维化,防止慢性脑积水的发生并改善蛛网膜下腔出血后的长期神经认知缺陷。LSKL, Inhibitor of Thrombospondin (TSP-1) TFA 可以轻松穿越血脑屏障。
LSKL, Inhibitor of Thrombospondin (TSP-1) (TFA) Chemical Structure
规格 | 价格 | 是否有货 | 数量 |
---|---|---|---|
10;mM;*;1 mL in DMSO | ¥1134 | In-stock | |
5 mg | ¥900 | In-stock | |
10 mg | ¥1300 | In-stock | |
25 mg | ¥2600 | In-stock | |
50 mg | ; | 询价 | ; |
100 mg | ; | 询价 | ; |
* Please select Quantity before adding items.
生物活性 |
LSKL, Inhibitor of Thrombospondin (TSP-1) TFA is a latency-associated protein (LAP)-TGFβ derived tetrapeptide and a competitive TGF-β1 antagonist. LSKL, Inhibitor of Thrombospondin (TSP-1) TFA inhibits the binding of TSP-1 to LAP and alleviates renal interstitial fibrosis and hepatic fibrosis. LSKL, Inhibitor of Thrombospondin (TSP-1) TFA suppresses subarachnoid fibrosis via inhibition of TSP-1-mediated TGF-β1 activity, prevents the development of chronic hydrocephalus and improves long-term neurocognitive defects following subarachnoid hemorrhage (SAH). LSKL, Inhibitor of Thrombospondin (TSP-1) TFA can readily crosse the blood-brain barrier[1][2]. |
IC50 Target |
TGF-β1[1] |
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体外研究 (In Vitro) |
The KTFR sequence from ADAMTS1 is responsible for the interaction with the LSKL, Inhibitor of Thrombospondin (TSP-1) (LSKL peptide) from the latent form of TGF-β, leading to its activation. There is a stable binding mode between LSKL, Inhibitor of Thrombospondin (TSP-1) and ADAMTS1 KTFR sequence, characterized by 3 salt bridges and 2 hydrogen bonds[2]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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体内研究 (In Vivo) |
LSKL, Inhibitor of Thrombospondin (TSP-1) (1 mg/kg; intraperitoneal injection; male Sprague-Dawley rats) is protective against subarachnoid fibrosis, attenuates ventriculomegaly and effectively suppresses hydrocephalus. LSKL, Inhibitor of Thrombospondin (TSP-1) treatment inhibits TGF-β1 activity and subsequent Smad2/3 signaling[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
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分子量 |
572.62 |
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Formula |
C23H43F3N6O7 |
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Sequence |
Leu-Ser-Lys-Leu |
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Sequence Shortening |
LSKL |
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中文名称 |
LSKL, 血小板反应蛋白抑制剂 (TSP-1) 三氟醋酸盐 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
Sealed storage, away from moisture
*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (sealed storage, away from moisture) |
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溶解性数据 |
In Vitro:;
DMSO : 250 mg/mL (436.59 mM; Need ultrasonic) H2O : 100 mg/mL (174.64 mM; Need ultrasonic) 配制储备液
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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