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SIGMA A3157-10G 阿尔新蓝8GX 33864-

99-2
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  • ¥2265
  • Sigma-Aldrich
  • 进口
  • A3157-10G
  • 2025年07月12日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      常温

    • 保质期

      根据瓶身LOT号查询

    • 英文名

      Alcian Blue 8GX

    • 库存

      有现货

    • 供应商

      浙江羽翔生物科技有限公司

    • CAS号

      33864-99-2

    • 规格

      10G

    属性

    产品名称

    阿尔新蓝 8GX, certified by the Biological Stain Commission

    等级

    certified by the Biological Stain Commission

    质量水平

    200

    表单

    powder

    组成

    Dye content, ≥50%

    技术

    microbe id | staining: suitable

    颜色

    dark blue

    溶解性

    water: 1 mg/mL, blue

    εmax

    195-400 at 617-630 nm

    应用

    diagnostic assay manufacturing
    hematology
    histology

    储存温度

    room temp

    SMILES字符串

    [Cl-].[Cl-].[Cl-].[Cl-].CN(C)C(\SCc1ccc2c3nc(nc4n5[Cu]n6c(nc7nc(nc5c8cc(CS\C(N(C)C)=[N+](\C)C)ccc48)c9ccc(CS\C(N(C)C)=[N+](\C)C)cc79)c%10ccc(CS\C(N(C)C)=[N+](\C)C)cc%10c6n3)c2c1)=[N+](/C)C

    InChI

    1S/C56H68N16S4.4ClH.Cu/c1-65(2)53(66(3)4)73-29-33-17-21-37-41(25-33)49-57-45(37)62-50-43-27-35(31-75-55(69(9)10)70(11)12)19-23-39(43)47(59-50)64-52-44-28-36(32-76-56(71(13)14)72(15)16)20-24-40(44)48(60-52)63-51-42-26-34(18-22-38(42)46(58-51)61-49)30-74-54(67(5)6)68(7)8;;;;;/h17-28H,29-32H2,1-16H3;4*1H;/q+2;;;;;+2/p-4

    InChI key

    CKLBXIYTBHXJEH-UHFFFAOYSA-J

    应用

    阿尔新蓝8GX(Alcian Blue 8GX )已可用于小鼠MPC(间充质祖细胞)结节中硫酸化蛋白多糖的染色。它已可用于牛关节软骨细胞中硫酸化蛋白多糖的染色。

    生化/生理作用

    阿尔新蓝8GX是一种阳离子染料。它与酸性糖胺聚糖形成不溶性复合物,从而有助于糖胺聚糖的定量测定。它还被用于骨和软骨的染色。

    适用性

    经认证可用于Mowry′s pH 2.5方法、Scott′s pH 5.7方法以及Kreyberg′s方法中的角蛋白和粘蛋白染色。

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    图标文献和实验
    该产品被引用文献

    Sarcopenia in osteoarthritis and rheumatoid arthritis: The association with self-reported fatigue, physical function and obesity.

    PloS one (2019-06-07)
    Lara Vlietstra, Simon Stebbings, Kim Meredith-Jones, J Haxby Abbott, Gareth J Treharne, Debra L Waters
    PMID31170172
    摘要

    To determine if there is an association between sarcopenia, physical function and self-reported fatigue in osteoarthritis (OA) and rheumatoid arthritis (RA). A cross-sectional analysis of measurements from a cohort of 157 participants with OA or RA was performed. The relationship between muscle mass (appendicular muscle index (AMI)), physical function (timed up and go, 30-seconds sit-to-stand test, 40-meter fast-paced walk test and grip-strength) and two fatigue measures (Multidimensional Assessment of Fatigue (MAF) and a fatigue Visual Analogue Scale (VAS)) was explored using hierarchical linear regression or logistic regression with established AMI cut-offs for sarcopenia. There were no significant differences for perceived fatigue-related variables between OA or RA sarcopenic or non-sarcopenic participants. Participants with OA had worse physical function (TUG; P = 0.029, STS; P = 0.004, WS; P = 0.003), but participants with RA had lower grip strength (P<0.001). The RA group had higher CRP (P = 0.006), were more likely to receive glucocorticoids (P<0.001), and experienced worse fatigue (P = 0.050). The hierarchical multiple regression showed that self-reported fatigue (VAS/MAF-distress) had a significant but weak association with AMI in RA. Participants with higher percentage body fat had a significantly stronger association with sarcopenia in both OA and RA. Sarcopenia, when assessed by AMI, does not appear to be strongly associated with self-reported fatigue or physical function in participants with either OA or RA. Higher body fat had a moderately strong association with sarcopenia in this cross-sectional study, suggesting that body composition may be an important factor in the health of patients with longstanding OA or RA.

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