刺五加皂苷 B
Ciwujianoside B 是一种具有口服活性且可穿透血脑屏障的辐射防护剂和记忆增强剂。Ciwujianoside B 减少辐射诱导的 DNA 损伤、细胞周期阻滞和凋亡 (apoptosis)、下调 NF-κB 和 Bax/Bcl-2 比值，增强骨髓细胞增殖能力。Ciwujianoside B 可增强正常小鼠的物体识别记忆，并诱导原代培养皮质神经元的树突延伸。Ciwujianoside B 可用于造血系统辐射损伤和记忆增强相关研究。
王不留行环肽 B
Segetalin B 是一种具有口服活性的环五肽，发现于 Vaccaria segetalis，具有雌激素样活性。Segetalin B 促进体外卵巢切除大鼠骨髓间充质干细胞矿化，提高骨钙素、BMP-2、ALP 和 SIRT1 活性水平。Segetalin B 有望用于绝经后骨质疏松症 (PMOP) 的研究。
锌(II)中卟啉IX
Zn (II) Mesoporphyrin IX (ZnMP) 是一种具有光化学底物活性的血红素加氧酶 (heme oxygenase) 抑制剂。Zn (II) Mesoporphyrin IX 能够特异性抑制骨髓血红素加氧酶的活性。Zn (II) Mesoporphyrin IX 在体外可抑制兔骨髓红系和髓系祖细胞的生长，并阻断 rhG-CSF 诱导的这些祖细胞向外周血的动员，显示出对兔造血生长及祖细胞生成的毒性。Zn (II) Mesoporphyrin IX 在 95% 乙醇溶液中经 UV-B 照射会发生符合一级动力学特征的不可逆光化学分解。Zn (II) Mesoporphyrin IX 可用于造血调控研究，但需注意其光不稳定性及对造血系统的毒性作用。
Eupenicisirenin C 是一种 Sirenin 衍生物。Eupenicisirenin C 具有很强的 NF-κB 抑制活性。Eupenicisirenin C 抑制对 cGAS-STING 通路的影响。Eupenicisirenin C 抑制骨髓巨噬细胞中 RANKL 诱导的破骨细胞分化。
刺五加皂苷 B (标准品)
Ciwujianoside B (Standard)是 Ciwujianoside B 的分析标准品。本产品用于研究及分析应用。Ciwujianoside B 是从 Eleutherococcus senticosus 叶中分离出来的，口服后能够渗透并在大脑中起作用。 Ciwujianoside B 显着增强识别记忆的能力。
Ciwujianoside B 显示对小鼠造血系统的辐射保护作用，其与细胞周期的变化，DNA 损伤的减少和暴露于辐射的骨髓细胞中 Bax/Bcl-2 比率的下调相关。
锌(II)中卟啉IX
Zn (II) Mesoporphyrin IX (ZnMP) 是一种具有光化学底物活性的血红素加氧酶 (heme oxygenase) 抑制剂。Zn (II) Mesoporphyrin IX 能够特异性抑制骨髓血红素加氧酶的活性。Zn (II) Mesoporphyrin IX 在体外可抑制兔骨髓红系和髓系祖细胞的生长，并阻断 rhG-CSF 诱导的这些祖细胞向外周血的动员，显示出对兔造血生长及祖细胞生成的毒性。Zn (II) Mesoporphyrin IX 在 95% 乙醇溶液中经 UV-B 照射会发生符合一级动力学特征的不可逆光化学分解。Zn (II) Mesoporphyrin IX 可用于造血调控研究，但需注意其光不稳定性及对造血系统的毒性作用。
王不留行环肽 B
Segetalin B 是一种具有口服活性的环五肽，发现于 Vaccaria segetalis，具有雌激素样活性。Segetalin B 促进体外卵巢切除大鼠骨髓间充质干细胞矿化，提高骨钙素、BMP-2、ALP 和 SIRT1 活性水平。Segetalin B 有望用于绝经后骨质疏松症 (PMOP) 的研究。
MCE 油红 O 染色试剂盒 (细胞涂片专用) 可有效染色各种大小的脂滴，包括较小的脂滴，且能够从溶剂中优先吸附染料。适用于细胞涂片、骨髓涂片、体液涂片、血液涂片等的油红 O 染色。使用时，标本不应采用含有乙醇的固定液。若需要固定，可使用 10% 福尔马林。脂肪的阳性染色结果通常呈橘黄色至红色，但具体颜色会根据脂质浓度有所不同。
刺五加皂苷 B
Ciwujianoside B 是一种具有口服活性且可穿透血脑屏障的辐射防护剂和记忆增强剂。Ciwujianoside B 减少辐射诱导的 DNA 损伤、细胞周期阻滞和凋亡 (apoptosis)、下调 NF-κB 和 Bax/Bcl-2 比值，增强骨髓细胞增殖能力。Ciwujianoside B 可增强正常小鼠的物体识别记忆，并诱导原代培养皮质神经元的树突延伸。Ciwujianoside B 可用于造血系统辐射损伤和记忆增强相关研究。
王不留行环肽 B
Segetalin B 是一种具有口服活性的环五肽，发现于 Vaccaria segetalis，具有雌激素样活性。Segetalin B 促进体外卵巢切除大鼠骨髓间充质干细胞矿化，提高骨钙素、BMP-2、ALP 和 SIRT1 活性水平。Segetalin B 有望用于绝经后骨质疏松症 (PMOP) 的研究。
Eupenicisirenin C 是一种 Sirenin 衍生物。Eupenicisirenin C 具有很强的 NF-κB 抑制活性。Eupenicisirenin C 抑制对 cGAS-STING 通路的影响。Eupenicisirenin C 抑制骨髓巨噬细胞中 RANKL 诱导的破骨细胞分化。
刺五加皂苷 B (标准品)
Ciwujianoside B (Standard)是 Ciwujianoside B 的分析标准品。本产品用于研究及分析应用。Ciwujianoside B 是从 Eleutherococcus senticosus 叶中分离出来的，口服后能够渗透并在大脑中起作用。 Ciwujianoside B 显着增强识别记忆的能力。
Ciwujianoside B 显示对小鼠造血系统的辐射保护作用，其与细胞周期的变化，DNA 损伤的减少和暴露于辐射的骨髓细胞中 Bax/Bcl-2 比率的下调相关。
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.
