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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Store at RT
- 保质期:
Store at RT
- 英文名:
Alcian Blue 8GX
- 库存:
现询
- 供应商:
北京索莱宝科技有限公司
- CAS号:
33864-99-2
- 规格:
1g/500mg/200mg
| 规格: | 1g | 产品价格: | ¥520.0 |
|---|---|---|---|
| 规格: | 500mg | 产品价格: | ¥340.0 |
| 规格: | 200mg | 产品价格: | ¥180.0 |
阿利新蓝(Alcian)又称爱先蓝或阿尔辛蓝等,是一种类铜钛花青共轭染料。这种阳离子染料与酸性基团结合,即阿尔辛蓝与组织内含有的阴离子基团如羧基和硫酸根形成不溶性复合物。阿利新蓝由中央含铜的酞菁环与四个异Thiourea基通过硫醚键相连而成。该异Thiourea基呈中度碱性,使阿利新蓝带阳离子。阿利新蓝使碳水化合物着色的确切机制不明,普遍认为是阳离子的异Thiourea基通过静电与组织内的多聚阴离子相连。如含羧基和硫酸根的酸性黏液物质的羧基和硫酸根形成不溶性复合物,即染料分子中带正电荷的盐键和酸性黏液物质中带负电荷的酸性基团结合呈蓝色。
利用染液的不同pH 值可区分粘液物质的类属:
pH 值为 2.5 时组织内的羧基电离, 带有一个负电荷, 与阿利新蓝中的阳离子形成盐键,是带有羧基的组织(如蛋白多糖/透明质酸以及上皮酸性黏蛋白)染色。
pH 值为 1.0 时,组织内的硫酸根电离,带有一个负电荷,与阿利新蓝中的阳离子形成盐键,使带有硫酸根的组织(如硫酸黏液物质)染色。中性黏蛋白(如胃黏膜和 Brunner 腺体部位的中性黏蛋白)不能与阿利新蓝反应。
软骨染色中:pH为1时,羧基(COOH)不着色,硫酸基(OSO3H)着色,pH为 2.5 时,羧基染色良好而硫酸粘液着色不佳,使硫酸黏蛋白和唾液黏蛋白着色。
本试剂仅适用于科研领域,不适用于临床诊断或其他用途。
使用方法(仅供参考)
1 改良 Lison 法∶
骨髓片甲醇固定5 min,水洗,风干;阿利新蓝液(10 g/L 阿利新蓝水溶液 100 mL和1%醋酸 100 mL 混合后过滤)染 30 min,充分水洗;1 g/L中性红水溶液复染 30 s,水洗,风干,镜检。
2 Mowry法∶
固定骨髓片5 min,水洗;阿利新蓝液(阿利新蓝1g,3%醋酸100 mL)染5~10 min,充分水洗,1 g/L中性红水渗液复染 30 s,水洗,风干,镜检。
3 Lev法∶
新鲜涂片甲醇固定5 min,水洗;阿利新蓝液(阿利新蓝1 g,0.1 mol/L盐酸 100 mL)染 10~30 min,充分水洗;1 g/L中性红水溶液复染30 s,水洗,风干,镜检。
In Vitro
Cell(rat bone mesenchymal stem cells (rBMSCs))
Chondrogenic di?erentiation of rBMSCs on the prepared membranes was evaluated through alcian blue staining. After sterilization, the membrane with the size of 15 mm × 15 mm was mounted on the CellCrown transwell and ?xed into a 24-well culture plate. Cells at passage 2 were seeded on the membranes at the density of 75,000 cells per membrane and cultured for 2 days to allow for optimal attachment. Cells seeded onto the culture plate were set as the blank control. The cell culture medium was then replaced by the chondrogenic induction medium for further induction. The medium was refreshed every 2 days. After induction for 7, 14, and 21 days respectively, Alcian blue staining (Solarbio, cat# IA2460) was performed according to the manufacturer’s instructions, and the stained samples were then imaged.
来源文献:Zhu Y, Dai B, Zhang S, Liu J, Xu S, Liu W, Chen X, Zhang H, Li Q, Pang FO, Li W, Wen C, Qin L, Xu J, Ngai T. Tissue Mimetic Membranes for Healing Augmentation of Tendon-Bone Interface in Rotator Cuff Repair. Adv Mater. 2025 Jan 31:e2407358. doi: 10.1002/adma.202407358. Epub ahead of print. PMID: 39888084.
【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
标题:OTUB1 promotes osteoblastic bone formation through stabilizing FGFR2
成员:Zhu Qiong, Fu Yesheng, Cui Chun-Ping, Ding Yi, Deng Zhikang, Ning Chao, Hu Fan, Qiu Chen, Yu Biyue, Zhou Xuemei, Yang Guan, Peng Jiang, Zou Weiguo, Liu Cui Hua, Zhang Lingqiang
论文因子:38.104 发表期刊:Signal Transduction and Targeted Therapy pmid:37024477
【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
标题:Nrf2 activation is involved in osteogenic differentiation of periodontal ligament stem cells under cyclic mechanical stretch
成员:Xi X; Zhao Y; Liu H; Li Z; Chen S; Liu D
论文因子:3.7 发表期刊:Exp Cell Res pmid:33865812
【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
标题:Conditional ablation of MAPK7 expression in chondrocytes impairs endochondral bone formation in limbs and adaptation of chondrocytes to hypoxia
成员:YangX;ZhongD;GaoW;LiaoZ;ChenY;ZhangS;ZhouH;SuP;XuC
论文因子:6.068 发表期刊:Cell Biosci pmid:32944217
【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
标题:lncRNA-CRNDE regulates BMSC chondrogenic differentiation and promotes cartilage repair in osteoarthritis through SIRT1/SOX9
成员:Shi C. Zheng W. Wang J
论文因子:3.108 发表期刊:Mol Cell Biochem pmid:33479807
| 基本信息 | |
| CAS | No.33864-99-2 |
| 中文名称 | 阿利新蓝8GX |
| 英文名称 | Alcian Blue 8GX |
| 分子式 | C56H68Cl4CuN16S4 |
| 分子量 | 1298.86 |
| 溶解性 | Soluble in Water ≥3mg/mL |
| 外观(性状) | Purple to black Solid |
| 储存条件 | Store at RT |
| EC | EINECS 278-333-8 |
| MDL | MFCD00010720 |
| SMILES | CN(C)C(=[N+](C)C)SCC1=CC2=C(C=C1)C3=NC4=NC(=NC5=C6C=C(C=CC6=C([N-]5)N=C7C8=C(C=CC(=C8)CSC(=[N+](C)C)N(C)C)C(=N7)N=C2[N-]3)CSC(=[N+](C)C)N(C)C)C9=C4C=C(C=C9)CSC(=[N+](C)C)N(C)C.[Cl-].[Cl-].[Cl-].[Cl-].[Cu+2] |
| 背景说明 | 是一种类铜钛花青共轭染料。 |
| 生物活性 | Alcian Blue 8GX is a commonly used phthalocyanine dye that binds to glycoproteins and glycosaminoglycans. Alcian Blue 8GX has a wide range of applications in biological staining, including proteins in brain tumors and DNA in cells and tissues[1][2][3][4]. |
| In Vitro | Isolation and culture of cranial NCCs in vitro facilitates screening and analyses of molecular cellular mechanisms of cranial NCCs implicated in craniofacial development. Here, we present a method for the isolation and culture of cranial NCCs harvested from the first branchial arch at early embryonic stages. Morphology of isolated cranial NCCs was similar to O9-1 cells, a cell line for neural crest stem cells.Moreover, cranial NCCs isolated from a transgenic mouse line with enhanced bone morphogenetic protein (BMP) signaling in NCCs showed an increase in their chondrogenic differentiation capacity, suggesting maintenance of their in vivo differentiation potentials observed in vitro.[1] |
| 数据来源文献 | [1]. Hiroki Ueharu, et al. Isolation and Culture of Cranial Neural Crest Cells from the First Branchial Arch of Mice. Bio Protoc. 2022 Apr 5;12(7):e4371. [2]. J Tas, et al. The Alcian blue and combined Alcian blue--Safranin O staining of glycosaminoglycans studied in a model system and in mast cells. Histochem J. 1977 Mar;9(2):205-30. [3]. Brian G Redfern, et al. An alternative Alcian Blue dye variant for the evaluation of fetal cartilage. Birth Defects Res B Dev Reprod Toxicol. 2007 Jun;80(3):171-6. [4]. Yuan Fang Li, et al. Determination of Proteins Based on Their Resonance Light Scattering Enhancement Effect on Alcian Blue 8GX. Original Papers. 2000 Dec; VOL.16 |
| 单位 | 瓶 |
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文献和实验【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
标题:OTUB1 promotes osteoblastic bone formation through stabilizing FGFR2
成员:Zhu Qiong, Fu Yesheng, Cui Chun-Ping, Ding Yi, Deng Zhikang, Ning Chao, Hu Fan, Qiu Chen, Yu Biyue, Zhou Xuemei, Yang Guan, Peng Jiang, Zou Weiguo, Liu Cui Hua, Zhang Lingqiang
论文因子:38.104 发表期刊:Signal Transduction and Targeted Therapy pmid:37024477
【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
标题:Nrf2 activation is involved in osteogenic differentiation of periodontal ligament stem cells under cyclic mechanical stretch
成员:Xi X; Zhao Y; Liu H; Li Z; Chen S; Liu D
论文因子:3.7 发表期刊:Exp Cell Res pmid:33865812
【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
标题:Conditional ablation of MAPK7 expression in chondrocytes impairs endochondral bone formation in limbs and adaptation of chondrocytes to hypoxia
成员:YangX;ZhongD;GaoW;LiaoZ;ChenY;ZhangS;ZhouH;SuP;XuC
论文因子:6.068 发表期刊:Cell Biosci pmid:32944217
【本资料源自公开渠道,如需(此处)屏蔽,请联系删除】
标题:lncRNA-CRNDE regulates BMSC chondrogenic differentiation and promotes cartilage repair in osteoarthritis through SIRT1/SOX9
成员:Shi C. Zheng W. Wang J
论文因子:3.108 发表期刊:Mol Cell Biochem pmid:33479807
好的选择。另外一种可供选择的方法是用不同的试剂来标记蛋白质至饱和来避免这种问题,这种方法有所报道 [11] ,但没有被广泛使用。 来自于 DIGE 的量化分析的意义是另外一个争论热点。这种体系现在只有 Amer-sham Biosciences ( GE Health care 的一部分)拥有,但非常昂贵。合成并使用商业化的蓝色染料 N-羟基丁二酰亚胺活化酯可避免这个问题 [12] 。deCyder 软件可以识别蛋白质表达变化,统计学上非常有意义。用软件模式比较荧光强度相对于传统的手工调节图像的亮度
光标记配体的测定可以获得不少有关结构参量和功能参量的信息。用于这方面工作的荧光探针主要有FITC、罗丹明系列(如四甲基异硫氰酸罗丹明TRITC、异硫氰酸罗丹明X-RITC和美国德州红等)、藻胆蛋白系列等。 2.2.4生物活性 生物活性的测定主要包括两方面:① 细胞本身的死活;② 活细胞生物功能发挥的强弱。FCM用来判断细胞死活的常用荧光探针有两大类:一类是能透过活细胞膜进入细胞内而发出荧光的物质,例如二乙酸荧光素(FDA,Fluorescein diacetate),它可被活细胞滞留而发出黄绿
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