(18420-1-AP)
用户验证的应用
经验证应用
| 项目 | 详情 |
|---|---|
| Positive WB detected in | HeLa cells, HEK-293 cells, NCI-H1299 cells, U2OS cells, HepG2 cells, Jurkat cells, U-87 MG cells |
| Positive IP detected in | HepG2 cells, U2OS cells |
| Positive IHC detected in | human lung cancer tissue, human gliomas tissue, human liver cancer tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
| Positive IF/ICC detected in | Chloroquine treated HepG2 cells, U2OS cells, Chloroquine treated HeLa cells |
| Positive FC (Intra) detected in | HEK-293 cells |
推荐稀释比例
- Western Blot (WB)1:5000-1:50000
- Immunoprecipitation (IP)0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
- Immunohistochemistry (IHC)1:200-1:800
- Immunofluorescence (IF)/ICC1:750-1:3000
- Flow Cytometry (FC) (INTRA)0.25 ug per 10^6 cells in a 100 µl suspension
推荐稀释说明
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. Sample-dependent, Check data in validation data gallery.
详细信息
背景信息
Background P62 (ubiquitin-binding protein P62), also known as Sequestosome-1, is a multifunctional adaptor protein most widely known for its role as an autophagosome cargo protein (PMID: 8551575). P62 via specific interactions with polyubiquitylated target proteins induces their selective autophagy (PMID: 17580304). It also plays an important role in the regulation of the NFkB signaling pathway, senescence, cell differentiation, apoptosis, and immune responses (PMID: 26404812). What is the molecular weight of P62? The observed molecular weight of the protein can vary from as low as 8 kDa (for the smallest isoforms) to 48 kDa. What is the subcellular localization of P62? P62 is mainly localized in the cytoplasm; however, upon autophagy induction, e.g., via starvation or selective inhibitor treatment, it localizes in vesicular structures - autophagosomes. What is the tissue specificity of P62? It is ubiquitously expressed in various tissues. What is the function of P62 in the regulation of cell death and autophagy? It is a selective autophagy receptor that forms a bridge between polyubiquitylated cargo (via its UBA domains) and an autophagy modifier such as LC3 (via LIR domains) (PMIDs: 16286508, 20168092, 24128730, 28404643, 22622177). The process of selective autophagy is tightly regulated at many levels, including the posttranslational modifications (PTMs) of various proteins in the cascade, P62 among others (PMID: 29233872). P62 is involved in the regulation of cell death induction in response to various stimuli, e.g., via activation of caspase-8 at the autophagosome membrane (PMID: 29480462). In addition, P62 is degraded during the autophagic process, which makes its intracellular level a marker for autophagy progression. What is P62's involvement in disease? Mutations in P62 have been associated with the following diseases: sporadic and familial Paget's disease of bone, neurodegenerative diseases, diabetes, and obesity (PMID: 29480462). A growing number of reports suggest the implication of P62 in the induction of multiple cellular oncogenic transformations. Indeed, increased levels of P62 have been linked to tumor formation, cancer promotion, and resistance to therapy (PMID: 29738493). Moreover, P62 is an unfavorable prognostic marker in liver cancer.
文献引用 (630)
NAP1L1 degradation by FBXW7 reduces the deubiquitination of HDGF-p62 signaling to stimulate autophagy and induce primary cisplatin chemosensitivity in nasopharyngeal carcinoma.
FBXW7 介导的 NAP1L1 降解减少了 HDGF-p62 信号的去泛素化,从而刺激自噬并诱导鼻咽癌对顺铂化疗的敏感性
Biomimetic Nanoparticles Simultaneously Targeting Modulation of Lipid Metabolism and Phenotype of Macrophages for Programmed Atherosclerosis Management.
仿生纳米颗粒同时靶向调节脂质代谢和巨噬细胞表型,用于程序性动脉粥样硬化管理
DSS1 inhibits autophagy to activate epithelial-mesenchymal transition in a pro-metastatic niche of renal cell carcinoma.
DSS1抑制自噬,从而激活肾细胞癌促转移微环境中的上皮-间质转化
RNF167 mediates atypical ubiquitylation and degradation of RLRs via two distinct proteolytic pathways.
RNF167 通过两种不同的蛋白水解途径介导 RLR 的非典型泛素化和降解
In situ architecture of the intercellular organelle reservoir between epididymal epithelial cells by volume electron microscopy.
利用体积电子显微镜观察附睾上皮细胞间细胞器库的原位结构
USP19 potentiates autophagic cell death via inhibiting mTOR pathway through deubiquitinating NEK9 in pancreatic cancer.
USP19 通过去泛素化 NEK9 抑制 mTOR 通路,从而增强胰腺癌细胞的自噬性细胞死亡
TRIM21-driven K63-linked ubiquitination of RBM38c, as a novel interactor of BECN1, contributes to DNA damage-induced autophagy.
TRIM21 驱动的 RBM38c 的 K63 连接的泛素化,作为 BECN1 的新型相互作用蛋白,促进 DNA 损伤诱导的自噬
IGF2BP3-mediated m(6)A modification of RASGRF1 promoting joint injury in rheumatoid arthritis.
IGF2BP3 介导的 RASGRF1 m(6)A 修饰促进类风湿性关节炎的关节损伤
Chaperone-mediated autophagy directs a dual mechanism to balance premature senescence and senolysis to prevent intervertebral disc degeneration.
分子伴侣介导的自噬指导双重机制,以平衡过早衰老和衰老细胞清除,从而防止椎间盘退变
Zika virus disrupts steroidogenesis and impairs spermatogenesis by stalling the translation of CYP17A1 mRNA
寨卡病毒通过阻断CYP17A1 mRNA的翻译来干扰类固醇生成并损害精子发生。
- 1
- 2
- 3
- 4
- 5
- 6
- 63