Aniline blue diammonium 是常用多色染色剂的组分。Aniline blue diammonium 用于染色组织切片中的胶原纤维，使用 Masson 三色方案染色多种成分。用这种方法可将胶原染成蓝色，该染料适用于植物标本中胼胝质的选择性染色和组蛋白染色，以评估核成熟度。Aniline blue diammonium 用于Gomori的一步三色染色剂和Mallory的结缔组织染色剂，适用于肾脏和肠道等组织。
GSK-2881078 是一种具有口服活性的非甾体选择性雄激素受体调节剂 (SARM)，在雄激素组织中作为部分 AR 激动剂，而在合成代谢组织中主要作为完全 AR 激动剂，在 PC3(AR)2 细胞中诱导 AR 介导的转录激活 (EC50 = 3.99 nM)，其效应可被非甾体 AR 拮抗剂 Bicalutamide 抑制。GSK-2881078 可用于慢性和急性疾病相关的肌无力和恶病质的研究。
Antcin K 是靶向 PI3K/Akt、NF-κB、MEK1/2-ERK、p38 及 AP-1 通路的选择性抑制剂。Antcin K 上调 IL-10 表达，进而抑制促炎因子产生、阻滞单核细胞黏附、减轻组织损伤并促进肌生成。Antcin K 具有显著的抗炎、抗损伤及组织保护活性。Antcin K 主要应用于牙周炎、类风湿关节炎、骨骼肌损伤等炎症相关疾病的研究。
Myelin Basic Protein (MHP4-14) 是一种合成肽，包含髓鞘碱性蛋白的残基4-14，是一种非常有选择性的PKC底物 (Km=7 μM)。Myelin Basic Protein 不被环腺苷酸依赖性蛋白激酶、酪蛋白激酶 I 和 II、Ca2+/钙调素依赖性蛋白激酶II或磷酸化酶激酶磷酸化，可常规用于测定粗组织提取物中低背景的蛋白激酶C。
Myelin Basic Protein (MHP4-14) TFA 是一种合成肽，包含髓鞘碱性蛋白的残基4-14，是一种非常有选择性的 PKC 底物 (Km=7 μM)。Myelin Basic Protein TFA 不被环腺苷酸依赖性蛋白激酶、酪蛋白激酶 I 和 II、Ca2+/钙调素依赖性蛋白激酶 II 或磷酸化酶激酶磷酸化，可常规用于测定粗组织提取物中低背景的蛋白激酶C。
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。
Aniline blue diammonium 是常用多色染色剂的组分。Aniline blue diammonium 用于染色组织切片中的胶原纤维，使用 Masson 三色方案染色多种成分。用这种方法可将胶原染成蓝色，该染料适用于植物标本中胼胝质的选择性染色和组蛋白染色，以评估核成熟度。Aniline blue diammonium 用于Gomori的一步三色染色剂和Mallory的结缔组织染色剂，适用于肾脏和肠道等组织。
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。
Myelin Basic Protein (MHP4-14) 是一种合成肽，包含髓鞘碱性蛋白的残基4-14，是一种非常有选择性的PKC底物 (Km=7 μM)。Myelin Basic Protein 不被环腺苷酸依赖性蛋白激酶、酪蛋白激酶 I 和 II、Ca2+/钙调素依赖性蛋白激酶II或磷酸化酶激酶磷酸化，可常规用于测定粗组织提取物中低背景的蛋白激酶C。
Myelin Basic Protein (MHP4-14) TFA 是一种合成肽，包含髓鞘碱性蛋白的残基4-14，是一种非常有选择性的 PKC 底物 (Km=7 μM)。Myelin Basic Protein TFA 不被环腺苷酸依赖性蛋白激酶、酪蛋白激酶 I 和 II、Ca2+/钙调素依赖性蛋白激酶 II 或磷酸化酶激酶磷酸化，可常规用于测定粗组织提取物中低背景的蛋白激酶C。
Antcin K 是靶向 PI3K/Akt、NF-κB、MEK1/2-ERK、p38 及 AP-1 通路的选择性抑制剂。Antcin K 上调 IL-10 表达，进而抑制促炎因子产生、阻滞单核细胞黏附、减轻组织损伤并促进肌生成。Antcin K 具有显著的抗炎、抗损伤及组织保护活性。Antcin K 主要应用于牙周炎、类风湿关节炎、骨骼肌损伤等炎症相关疾病的研究。
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.
![[Lys5,MeLeu9,Nle10]Neurokinin A(4-10)](http://hg.y866.cn/biomolecule/lib/file/product_pic/hy-p3849.gif)
