详细信息
特异性
Cross reactivity against Beta Galactosidase from other tissues and species may occur but have not been specifically determined. Very low background staining has been reported in various assays.
背景信息
Application Note: This antibody shows inconsistent results between batches in ICC/IF, IF, IHC-P, IHC-Fr and IHC-FoFr. We have received several good Abreviews on these applications, however, we are unable to guarantee positive results. If the antibody is used for IHC, please try fixing with methanol and block with gelatine instead with BSA or NGS. After each antibody incubation, please wash 5x with TBS instead of PBS.We would recommend ab4761 or ab12081 as alternatives.
文献引用 (64)
The Vitamin D-Sirt1/PGC1α Axis Regulates Bone Metabolism and Counteracts Osteoporosis
维生素 D-Sirt1/PGC1α 轴调节骨代谢并抵抗骨质疏松症
Development of a Hepatocyte-Specific Temporal Genetic Mouse Model Using Albumin Promoter-Driven FlpER2 Expression.
利用白蛋白启动子驱动的FlpER2表达，构建肝细胞特异性时间遗传小鼠模型。
Inhibiting Glutaminase Exerts Opposite Effects on Ovariectomy-Induced and Age-Related Reductions in Murine Bone Mass
抑制谷氨酰胺酶对卵巢切除术引起的和与年龄有关的小鼠骨量减少产生相反的影响
The senolytic agent ABT263 ameliorates osteoporosis caused by active vitamin D insufficiency through selective clearance of senescent skeletal cells
抗衰老药物 ABT263 通过选择性清除衰老骨骼细胞，改善因活性维生素 D 不足引起的骨质疏松症
Albumin promoter-driven FlpO expression induces efficient genetic recombination in mouse liver.
白蛋白启动子驱动的 FlpO 表达可诱导小鼠肝脏中有效的基因重组
1,25-Dihydroxyvitamin D Deficiency Accelerates Aging-related Osteoarthritis via Downregulation of Sirt1 in Mice
1,25-二羟基维生素 D 缺乏症通过下调小鼠 Sirt1 加速与衰老相关的骨关节炎
Patient-associated mutations in Drosophila Alk perturb neuronal differentiation and promote survival
果蝇Alk基因中与患者相关的突变会扰乱神经元分化并促进存活
Osteogenic differentiation of human mesenchymal stromal cells and fibroblasts differs depending on tissue origin and replicative senescence
人类间充质干细胞和成纤维细胞的成骨分化因组织来源和复制性衰老而异
Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles
鉴定针对 eEF1A2 并上调营养不良肌肉中 utrophin A 翻译的治疗方法
Loss of Cx43 in Murine Sertoli Cells Leads to Altered Prepubertal Sertoli Cell Maturation and Impairment of the Mitosis-Meiosis Switch
小鼠塞托利细胞 Cx43 缺失导致青春期前塞托利细胞成熟改变和有丝分裂-减数分裂转换受损
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