Anti-SQSTM1/p62泛素结合蛋白P62抗体

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bioss
国产
2021-09-09 19:26

上海恪敏生物科技有限公司

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上海恪敏生物科技有限公司
王羽
18021003406
1914109725@qq.com
产品属性
保存条件-20℃
宿主
是否单克隆2
抗体英文名Anti-SQSTM1/p62
供应商上海科敏
抗原来源详询
保质期1年
应用范围WB,IHC-P,IHC-F,ICC,IF, Elisa
适应物种hu, mo, rat, pig, shp, cow, hrs, dog, Rb
规格100ug
产品说明
本公司提供科研SQSTM1/p62泛素结合蛋白P62抗体,抗体质量可靠,订购SQSTM1/p62泛素结合蛋白P62抗体请联系在线客服或者销售人员。
抗体参数如下>>>>
中文名称:泛素结合蛋白P62抗体
英文名称:Anti-SQSTM1/p62
货号:bs-2951R
抗体来源:兔
克隆类型:多克隆
蛋白分子量:predicted molecular weight: 48kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, mo, rat, pig, shp, cow, hrs, dog, Rb
测试应用:ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500
(石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
产品背景介绍:Adapter protein which binds ubiquitin and may regulate the activation of NFKB1 by TNF-alpha, nerve growth factor (NGF) and interleukin-1. May play a role in titin/TTN downstream signaling in muscle cells. May regulate signaling cascades through ubiquitination. Adapter that mediates the interaction between TRAF6 and CYLD (By similarity). May be involved in cell differentiation, apoptosis, immune response and regulation of K(+) channels.Function : Adapter protein which binds ubiquitin and may regulate the activation of NFKB1 by TNF-alpha, nerve growth factor (NGF) and interleukin-1. May play a role in titin/TTN downstream signaling in muscle cells. May regulate signaling cascades through ubiquitination. Adapter that mediates the interaction between TRAF6 and CYLD (By similarity). May be involved in cell differentiation, apoptosis, immune response and regulation of K(+) channels.Subunit : Cytoplasm. Late endosome. Nucleus. Endoplasmic reticulum. Note=Sarcomere. In cardiac muscles localizes to the sarcomeric band. Localizes to late endosomes. May also localize to the nucleus. Accumulates in neurofibrillary tangles and in Lewy bodies of neurons from individuals with Alzheimer and Parkinson disease respectively. Enriched in Rosenthal fibers of pilocytic astrocytoma. In liver cells, accumulates in Mallory bodies associated with alcoholic hepatitis, Wilson disease, indian childhood cirrhosis and in hyaline bodies associated with hepatocellular carcinoma. Colocalizes with TRIM13 in the perinuclear endoplasmic reticulum.Subcellular Location : Cytoplasm. Late endosome. Nucleus. Sarcomere (By similarity). In cardiac muscles localizes to the sarcomeric band (By similarity). Localizes to late endosomes. May also localize to the nucleus. Accumulates in neurofibrillary tangles and in Lewy bodies of neurons from individuals with Alzheimer and Parkinson disease respectively. Enriched in Rosenthal fibers of pilocytic astrocytoma. In liver cells, accumulates in Mallory bodies associated with alcoholic hepatitis, Wilson disease, indian childhood cirrhosis and in hyaline bodies associated with hepatocellular carcinoma.Tissue Specificity : Ubiquitously expressed.Post-translational modifications : Phosphorylated. May be phosphorylated by PRKCZ (By similarity). Phosphorylated in vitro by TTN.DISEASE : Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:602080]. PDB is a metabolic bone disease affecting the axial skeleton and characterized by focal areas of increased and disorganized bone turn-over due to activated osteoclasts. Manifestations of the disease include bone pain, deformity, pathological fractures, deafness, neurological complications and increased risk of osteosarcoma. PDB is a chronic disease affecting 2 to 3% of the population above the age of 40 years.Similarity : Contains 1 OPR domain.Contains 1 UBA domain.Contains 1 ZZ-type zinc finger.