直接黑 38
Direct Black 38 (Chlorazol Black E) 是一种基于联苯胺的偶氮染料,是 Enterococcus gallinarum 的底物,主要用于纺织染色。Direct Black 38 经过微生物酶 (如鹑鸡肠球菌偶氮还原酶) 还原,对偶氮键断裂,释放出联苯胺和 4-氨基联苯等,实现生物降解。Direct Black 38 可用于环境毒理学、废水处理及致癌性研究,但其代谢产物联苯胺被列为人类致癌物。
酸性橙GG
Orange G 是一种常见于纺织废水中的偶氮染料,主要用于纺织品染色。Orange G 具有显色功能,能赋予纺织品特定颜色。而 Orange G 在环境中的稳定性和潜在危害,常被用于研究各种污水处理技术对难降解有机污染物的去除效果,尤其是针对偶氮染料的降解研究。相关研究聚焦于如何通过化学、物理或生物方法,破坏 Orange G 的偶氮键,实现无害化处理,以解决纺织废水污染问题。
Arsenazo III 是变色酸的偶氮衍生物、金属铬染料、螯合剂及阳离子络合剂。Arsenazo III 可与 Ca2+、Mg2+、Sr2+、Ba2+、K+和 Na+形成稳定的 1:1 络合物,且对 Ca2+的结合亲和力取决于 pH、碱金属阳离子浓度和缓冲液参数。Arsenazo III 可用作细胞中微摩尔级离子化 Ca2+的比色指示剂。
1号金莲橙000
Orange I (α-Naphthol Orange) 是一种阴离子型偶氮染料,可与 Methylene blue (HY-14536) 形成复合物,并发生荧光猝灭。Orange I 与 Methylene blue 的复合物的平衡常数为 79900 mol-1·dm3。Orange I 可改变自身及 Methylene blue 的吸收光谱。
赤藓红
Erythrosin B sodium salt,是一种合成偶氮染料,通常用作食品着色剂和纺织染料。它是一种水溶性化合物,可产生鲜红色,常用于改善产品的外观。Erythrosin B sodium salt 还用于纺织工业,对羊毛、丝绸和皮革进行染色。然而,它与潜在的负面健康影响有关,例如儿童的过敏反应和多动症。
苯胺黑
Solvent black 5 (Spirit nigrosine) 是一种属于偶氮染料家族的合成染料。又称油黑或萘酚黑,呈深蓝黑色,在有机溶剂中溶解性极佳。Solvent black 5 通常用作印刷油墨、涂料和塑料等各种工业应用中的着色剂。它还可以用作检测溶液中金属存在的指示剂染料。此外,由于其在近红外区域的高吸收和发射特性,它已在科学研究中用作组织和细胞的荧光生物标志物。然而,据报道,Solvent black 5 对人类健康和环境具有潜在的毒性作用,因此在一些国家/地区对其使用进行了管制。
直接黑 38
Direct Black 38 (Chlorazol Black E) 是一种基于联苯胺的偶氮染料,是 Enterococcus gallinarum 的底物,主要用于纺织染色。Direct Black 38 经过微生物酶 (如鹑鸡肠球菌偶氮还原酶) 还原,对偶氮键断裂,释放出联苯胺和 4-氨基联苯等,实现生物降解。Direct Black 38 可用于环境毒理学、废水处理及致癌性研究,但其代谢产物联苯胺被列为人类致癌物。
酸性橙GG
Orange G 是一种常见于纺织废水中的偶氮染料,主要用于纺织品染色。Orange G 具有显色功能,能赋予纺织品特定颜色。而 Orange G 在环境中的稳定性和潜在危害,常被用于研究各种污水处理技术对难降解有机污染物的去除效果,尤其是针对偶氮染料的降解研究。相关研究聚焦于如何通过化学、物理或生物方法,破坏 Orange G 的偶氮键,实现无害化处理,以解决纺织废水污染问题。
Arsenazo III 是变色酸的偶氮衍生物、金属铬染料、螯合剂及阳离子络合剂。Arsenazo III 可与 Ca2+、Mg2+、Sr2+、Ba2+、K+和 Na+形成稳定的 1:1 络合物,且对 Ca2+的结合亲和力取决于 pH、碱金属阳离子浓度和缓冲液参数。Arsenazo III 可用作细胞中微摩尔级离子化 Ca2+的比色指示剂。
赤藓红
Erythrosin B sodium salt,是一种合成偶氮染料,通常用作食品着色剂和纺织染料。它是一种水溶性化合物,可产生鲜红色,常用于改善产品的外观。Erythrosin B sodium salt 还用于纺织工业,对羊毛、丝绸和皮革进行染色。然而,它与潜在的负面健康影响有关,例如儿童的过敏反应和多动症。
苯胺黑
Solvent black 5 (Spirit nigrosine) 是一种属于偶氮染料家族的合成染料。又称油黑或萘酚黑,呈深蓝黑色,在有机溶剂中溶解性极佳。Solvent black 5 通常用作印刷油墨、涂料和塑料等各种工业应用中的着色剂。它还可以用作检测溶液中金属存在的指示剂染料。此外,由于其在近红外区域的高吸收和发射特性,它已在科学研究中用作组织和细胞的荧光生物标志物。然而,据报道,Solvent black 5 对人类健康和环境具有潜在的毒性作用,因此在一些国家/地区对其使用进行了管制。
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.