Cardiotoxin Analog (CTX) IV (6-12) 是一种特异性靶向带负电荷磷脂膜 (如磷脂酰丝氨酸、磷脂酰肌醇) 的膜活性肽段,能够从台湾眼镜蛇的毒液中分离得到。Cardiotoxin Analog (CTX) IV (6-12) 是一种蛇毒心脏毒素,通过疏水相互作用和静电吸引结合细胞膜、嵌入脂质双层,从而破坏膜结构稳定性。Cardiotoxin Analog (CTX) IV (6-12) 可诱导膜脂紊乱和细胞裂解,展现出溶血和细胞毒性。
Cardiotoxin Analog (CTX) IV (6-12) TFA 是一种特异性靶向带负电荷磷脂膜 (如磷脂酰丝氨酸、磷脂酰肌醇) 的膜活性肽段,能够从台湾眼镜蛇的毒液中分离得到。Cardiotoxin Analog (CTX) IV (6-12) TFA 是一种蛇毒心脏毒素,通过疏水相互作用和静电吸引结合细胞膜、嵌入脂质双层,从而破坏膜结构稳定性。Cardiotoxin Analog (CTX) IV (6-12) TFA 可诱导膜脂紊乱和细胞裂解,展现出溶血和细胞毒性。
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。
Celestine Blue 是DNA生物传感器中的一种电活性指示剂。Celestine Blue 在尖晶石相和碳纳米管 (CNT) 上具有很强的吸附作用,有利于分散,可作为旋盖剂,并可用于制造尖晶石装饰的碳纳米管。Celestine Blue 是一种高效的电荷转移介质,它允许显著改善电容行为。在丙型肝炎病毒 (HCV) 核心抗原的夹心免疫检测中,掺杂 Celestine Blue 的二氧化钛纳米颗粒可作为标记物。
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。
Celestine Blue 是DNA生物传感器中的一种电活性指示剂。Celestine Blue 在尖晶石相和碳纳米管 (CNT) 上具有很强的吸附作用,有利于分散,可作为旋盖剂,并可用于制造尖晶石装饰的碳纳米管。Celestine Blue 是一种高效的电荷转移介质,它允许显著改善电容行为。在丙型肝炎病毒 (HCV) 核心抗原的夹心免疫检测中,掺杂 Celestine Blue 的二氧化钛纳米颗粒可作为标记物。
Cardiotoxin Analog (CTX) IV (6-12) 是一种特异性靶向带负电荷磷脂膜 (如磷脂酰丝氨酸、磷脂酰肌醇) 的膜活性肽段,能够从台湾眼镜蛇的毒液中分离得到。Cardiotoxin Analog (CTX) IV (6-12) 是一种蛇毒心脏毒素,通过疏水相互作用和静电吸引结合细胞膜、嵌入脂质双层,从而破坏膜结构稳定性。Cardiotoxin Analog (CTX) IV (6-12) 可诱导膜脂紊乱和细胞裂解,展现出溶血和细胞毒性。
Cardiotoxin Analog (CTX) IV (6-12) TFA 是一种特异性靶向带负电荷磷脂膜 (如磷脂酰丝氨酸、磷脂酰肌醇) 的膜活性肽段,能够从台湾眼镜蛇的毒液中分离得到。Cardiotoxin Analog (CTX) IV (6-12) TFA 是一种蛇毒心脏毒素,通过疏水相互作用和静电吸引结合细胞膜、嵌入脂质双层,从而破坏膜结构稳定性。Cardiotoxin Analog (CTX) IV (6-12) TFA 可诱导膜脂紊乱和细胞裂解,展现出溶血和细胞毒性。
Cardiotoxin Analog (CTX) IV (6-12) 是一种特异性靶向带负电荷磷脂膜 (如磷脂酰丝氨酸、磷脂酰肌醇) 的膜活性肽段,能够从台湾眼镜蛇的毒液中分离得到。Cardiotoxin Analog (CTX) IV (6-12) 是一种蛇毒心脏毒素,通过疏水相互作用和静电吸引结合细胞膜、嵌入脂质双层,从而破坏膜结构稳定性。Cardiotoxin Analog (CTX) IV (6-12) 可诱导膜脂紊乱和细胞裂解,展现出溶血和细胞毒性。
Cardiotoxin Analog (CTX) IV (6-12) TFA 是一种特异性靶向带负电荷磷脂膜 (如磷脂酰丝氨酸、磷脂酰肌醇) 的膜活性肽段,能够从台湾眼镜蛇的毒液中分离得到。Cardiotoxin Analog (CTX) IV (6-12) TFA 是一种蛇毒心脏毒素,通过疏水相互作用和静电吸引结合细胞膜、嵌入脂质双层,从而破坏膜结构稳定性。Cardiotoxin Analog (CTX) IV (6-12) TFA 可诱导膜脂紊乱和细胞裂解,展现出溶血和细胞毒性。
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.