固绿 FCF
Fast Green FCF 是一种海绿色三芳基甲烷食用染料,最大吸收范围为 622 至 626 nm。Fast Green FCF 可抑制 α-synuclein 聚集,抑制 Aβ、P2X4 受体、TLR4/Myd88/NF-κB。Fast Green FCF 广泛用作染色剂,如在酸性提取 DNA 后在碱性 pH 下定量染色组蛋白,以及在电泳中用作蛋白质染色剂。Fast Green FCF 改善认知障碍、抑郁症、缓解疼痛过敏、促进生殖功能。
苏丹IV
Sudan IV 是一种芳香烃受体 (AhR) 的激动剂,可激活下游信号通路,诱导 CYP1A1 表达。Sudan IV 通过激活 AhR-ARNT 异二聚体,结合 DNA 上的外源性反应元件 (XRE),促进 CYP1A1 基因转录,从而增强药物代谢酶活性。Sudan IV 可用于研究工业染料的毒性机制、与血清蛋白 (如牛血清白蛋白 BSA) 的相互作用对体内分布的影响。Sudan IV 是一种脂溶性重氮染料、可用于冰冻切片上对脂类、甘油三酯和脂蛋白进行染色。
Methyl Green 是一种选择性结合 DNA 大沟的非嵌入性荧光标记剂。Methyl Green 通过带正电荷的基团与 DNA 大沟发生静电相互作用,展现出高亲和力、抗光漂白及稳定的荧光发射等关键活性。Methyl Green 可以通过显微镜和流式细胞术直接测定活性,峰值在 633 和 677 nm。Methyl Green 可用于胚胎组织或细胞的细胞核荧光标记、或凝胶电泳中 DNA 染色及细胞活性检测等。
NIR-Red Dead Cell-1 Dye 是一种非活细胞的 DNA 结合荧光染料 (Ex/Em=515 nm/531 nm)。NIR-Red Dead Cell-1 Dye 可嵌入双链 DNA 的碱基对,并产生更强的应该。NIR-Red Dead Cell-1 Dye 适用于细胞膜受损的坏死细胞或凋亡晚期细胞,在荧光显微镜或流式细胞术下呈现绿色荧光。NIR-Red Dead Cell-1 Dye 可用于区分活细胞与死细胞,区分细胞膜完整性。NIR-Red Dead Cell-1 Dye 可以附着在 Feraheme (FH) 纳米颗粒 (NP) 的表面,以获得荧光染料功能化的 NP,用于药物递送的研究。
二甲苯苯胺
Xylene Cyanol FF 是一种酸性三苯甲烷染料。Xylene Cyanol FF 可用于血红蛋白过氧化物酶的组织化学染色,或用作电泳中 DNA 测序的示踪染料。Xylene Cyanol FF 在双氧化剂过氧化氢与高碘酸钾添加下,会受到 Fe 和 Al 的催化而加快氧化。Xylene Cyanol FF 由此可以利用分光光度法测定待测溶液中 Fe 和 Al 的含量。
碱性蓝 26
Basic blue 26 (Victoria blue B) 是一种合成阳离子染料,属于三芳基甲烷染料。它具有明亮的蓝色,通常用作各种应用的着色剂,包括纺织品、纸张和皮革。Basic Blue 26 也用作实验室 DNA 和蛋白质检测的生物染色剂。由于它能够与带负电荷的材料结合,它可以用作生物样品中特定分子存在的指示剂。然而,据报道,Basic blue 26 对人类健康和环境有潜在的有害影响,其使用在一些国家受到管制。正确的处理和处置程序对于最大程度地减少其对环境的影响是必要的。
绿色核酸染料
SYTM Green 是一种不可渗透细胞膜的 DNA 染料 (Ex/Em=503/530 nm),通过与 dsDNA 结合而发出绿色荧光。SYTM Green 还可用于细菌染色,包括革兰氏阳性菌和革兰氏阴性菌。注:SYTM Green 不可透过活细胞,该产品等效 SYTOX Green (Ex/Em=488/530 nm)。
甲苯胺兰
Toluidine blue (ZnCl2) 是一种碱性噻嗪染料,通常用作显微镜检查的生物染色剂。它具有深蓝紫色,常用于对 DNA 和 RNA 等核酸进行染色,以及对肥大细胞、软骨和其他结缔组织进行染色。Toluidine blue (ZnCl2) 染色这些组织的酸性成分,例如硫酸化或羧化粘多糖。它经常用于组织学、细胞学和病理学应用,以帮助诊断各种疾病和病症。染料通常在显微镜检查之前应用于组织切片,并且可以使用酸性酒精溶液进行区分。Toluidine blue (ZnCl2) 是一种相对简单且廉价的染色剂,具有良好的重现性,使其成为许多实验室的流行选择。
苏丹IV (标准品)
Sudan IV (Standard) (Solvent Red 24 (Standard)) 是 Sudan IV (HY-D0932) 的分析标准品。本产品用于研究及分析应用。Sudan IV 是一种芳香烃受体 (AhR) 的激动剂,可激活下游信号通路,诱导 CYP1A1 表达。Sudan IV 通过激活 AhR-ARNT 异二聚体,结合 DNA 上的外源性反应元件 (XRE),促进 CYP1A1 基因转录,从而增强药物代谢酶活性。Sudan IV 可用于研究工业染料的毒性机制、与血清蛋白 (如牛血清白蛋白 BSA) 的相互作用对体内分布的影响。Sudan IV 是一种脂溶性重氮染料、可用于冰冻切片上对脂类、甘油三酯和脂蛋白进行染色。
Fast green FCF free acid 是耐酸性的染料。Fast Green FCF free acid 可抑制 α-synuclein 聚集,抑制 Aβ、P2X4 受体、TLR4/Myd88/NF-κB。Fast Green FCF free acid 广泛用作染色剂,如在酸性提取 DNA 后在碱性 pH 下定量染色组蛋白,以及在电泳中用作蛋白质染色剂。Fast Green FCF free acid 改善认知障碍、抑郁症、缓解疼痛过敏、促进生殖功能。
苏丹IV-d6
Sudan IV-d6 (Solvent Red 24-d6) 是氘代标记的 Sudan IV (HY-D0932)。Sudan IV 是一种芳香烃受体 (AhR) 的激动剂,可激活下游信号通路,诱导 CYP1A1 表达。Sudan IV 通过激活 AhR-ARNT 异二聚体,结合 DNA 上的外源性反应元件 (XRE),促进 CYP1A1 基因转录,从而增强药物代谢酶活性。Sudan IV 可用于研究工业染料的毒性机制、与血清蛋白 (如牛血清白蛋白 BSA) 的相互作用对体内分布的影响。Sudan IV 是一种脂溶性重氮染料、可用于冰冻切片上对脂类、甘油三酯和脂蛋白进行染色。
固绿 FCF
Fast Green FCF 是一种海绿色三芳基甲烷食用染料,最大吸收范围为 622 至 626 nm。Fast Green FCF 可抑制 α-synuclein 聚集,抑制 Aβ、P2X4 受体、TLR4/Myd88/NF-κB。Fast Green FCF 广泛用作染色剂,如在酸性提取 DNA 后在碱性 pH 下定量染色组蛋白,以及在电泳中用作蛋白质染色剂。Fast Green FCF 改善认知障碍、抑郁症、缓解疼痛过敏、促进生殖功能。
苏丹IV
Sudan IV 是一种芳香烃受体 (AhR) 的激动剂,可激活下游信号通路,诱导 CYP1A1 表达。Sudan IV 通过激活 AhR-ARNT 异二聚体,结合 DNA 上的外源性反应元件 (XRE),促进 CYP1A1 基因转录,从而增强药物代谢酶活性。Sudan IV 可用于研究工业染料的毒性机制、与血清蛋白 (如牛血清白蛋白 BSA) 的相互作用对体内分布的影响。Sudan IV 是一种脂溶性重氮染料、可用于冰冻切片上对脂类、甘油三酯和脂蛋白进行染色。
Methyl Green 是一种选择性结合 DNA 大沟的非嵌入性荧光标记剂。Methyl Green 通过带正电荷的基团与 DNA 大沟发生静电相互作用,展现出高亲和力、抗光漂白及稳定的荧光发射等关键活性。Methyl Green 可以通过显微镜和流式细胞术直接测定活性,峰值在 633 和 677 nm。Methyl Green 可用于胚胎组织或细胞的细胞核荧光标记、或凝胶电泳中 DNA 染色及细胞活性检测等。
NIR-Red Dead Cell-1 Dye 是一种非活细胞的 DNA 结合荧光染料 (Ex/Em=515 nm/531 nm)。NIR-Red Dead Cell-1 Dye 可嵌入双链 DNA 的碱基对,并产生更强的应该。NIR-Red Dead Cell-1 Dye 适用于细胞膜受损的坏死细胞或凋亡晚期细胞,在荧光显微镜或流式细胞术下呈现绿色荧光。NIR-Red Dead Cell-1 Dye 可用于区分活细胞与死细胞,区分细胞膜完整性。NIR-Red Dead Cell-1 Dye 可以附着在 Feraheme (FH) 纳米颗粒 (NP) 的表面,以获得荧光染料功能化的 NP,用于药物递送的研究。
二甲苯苯胺
Xylene Cyanol FF 是一种酸性三苯甲烷染料。Xylene Cyanol FF 可用于血红蛋白过氧化物酶的组织化学染色,或用作电泳中 DNA 测序的示踪染料。Xylene Cyanol FF 在双氧化剂过氧化氢与高碘酸钾添加下,会受到 Fe 和 Al 的催化而加快氧化。Xylene Cyanol FF 由此可以利用分光光度法测定待测溶液中 Fe 和 Al 的含量。
碱性蓝 26
Basic blue 26 (Victoria blue B) 是一种合成阳离子染料,属于三芳基甲烷染料。它具有明亮的蓝色,通常用作各种应用的着色剂,包括纺织品、纸张和皮革。Basic Blue 26 也用作实验室 DNA 和蛋白质检测的生物染色剂。由于它能够与带负电荷的材料结合,它可以用作生物样品中特定分子存在的指示剂。然而,据报道,Basic blue 26 对人类健康和环境有潜在的有害影响,其使用在一些国家受到管制。正确的处理和处置程序对于最大程度地减少其对环境的影响是必要的。
绿色核酸染料
SYTM Green 是一种不可渗透细胞膜的 DNA 染料 (Ex/Em=503/530 nm),通过与 dsDNA 结合而发出绿色荧光。SYTM Green 还可用于细菌染色,包括革兰氏阳性菌和革兰氏阴性菌。注:SYTM Green 不可透过活细胞,该产品等效 SYTOX Green (Ex/Em=488/530 nm)。
甲苯胺兰
Toluidine blue (ZnCl2) 是一种碱性噻嗪染料,通常用作显微镜检查的生物染色剂。它具有深蓝紫色,常用于对 DNA 和 RNA 等核酸进行染色,以及对肥大细胞、软骨和其他结缔组织进行染色。Toluidine blue (ZnCl2) 染色这些组织的酸性成分,例如硫酸化或羧化粘多糖。它经常用于组织学、细胞学和病理学应用,以帮助诊断各种疾病和病症。染料通常在显微镜检查之前应用于组织切片,并且可以使用酸性酒精溶液进行区分。Toluidine blue (ZnCl2) 是一种相对简单且廉价的染色剂,具有良好的重现性,使其成为许多实验室的流行选择。
苏丹IV (标准品)
Sudan IV (Standard) (Solvent Red 24 (Standard)) 是 Sudan IV (HY-D0932) 的分析标准品。本产品用于研究及分析应用。Sudan IV 是一种芳香烃受体 (AhR) 的激动剂,可激活下游信号通路,诱导 CYP1A1 表达。Sudan IV 通过激活 AhR-ARNT 异二聚体,结合 DNA 上的外源性反应元件 (XRE),促进 CYP1A1 基因转录,从而增强药物代谢酶活性。Sudan IV 可用于研究工业染料的毒性机制、与血清蛋白 (如牛血清白蛋白 BSA) 的相互作用对体内分布的影响。Sudan IV 是一种脂溶性重氮染料、可用于冰冻切片上对脂类、甘油三酯和脂蛋白进行染色。
Fast green FCF free acid 是耐酸性的染料。Fast Green FCF free acid 可抑制 α-synuclein 聚集,抑制 Aβ、P2X4 受体、TLR4/Myd88/NF-κB。Fast Green FCF free acid 广泛用作染色剂,如在酸性提取 DNA 后在碱性 pH 下定量染色组蛋白,以及在电泳中用作蛋白质染色剂。Fast Green FCF free acid 改善认知障碍、抑郁症、缓解疼痛过敏、促进生殖功能。
二甲苯苯胺
Xylene Cyanol FF 是一种酸性三苯甲烷染料。Xylene Cyanol FF 可用于血红蛋白过氧化物酶的组织化学染色,或用作电泳中 DNA 测序的示踪染料。Xylene Cyanol FF 在双氧化剂过氧化氢与高碘酸钾添加下,会受到 Fe 和 Al 的催化而加快氧化。Xylene Cyanol FF 由此可以利用分光光度法测定待测溶液中 Fe 和 Al 的含量。
Sudan IV-d6 (Solvent Red 24-d6) 是氘代标记的 Sudan IV (HY-D0932)。Sudan IV 是一种芳香烃受体 (AhR) 的激动剂,可激活下游信号通路,诱导 CYP1A1 表达。Sudan IV 通过激活 AhR-ARNT 异二聚体,结合 DNA 上的外源性反应元件 (XRE),促进 CYP1A1 基因转录,从而增强药物代谢酶活性。Sudan IV 可用于研究工业染料的毒性机制、与血清蛋白 (如牛血清白蛋白 BSA) 的相互作用对体内分布的影响。Sudan IV 是一种脂溶性重氮染料、可用于冰冻切片上对脂类、甘油三酯和脂蛋白进行染色。
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
MedchemExpress Validation 03
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
MedchemExpress Validation 04
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.