SQSTM1 抗体 (AA 232-356)
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- 抗原 See all SQSTM1 抗体
- SQSTM1 (Sequestosome 1 (SQSTM1))
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抗原表位
- AA 232-356
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This SQSTM1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)
- 纯化方法
- Purified
- 免疫原
- Purified recombinant fragment of human SQSTM1 (AA: 232-356) expressed in E. Coli.
- 克隆位点
- 5H7E2
- 亚型
- IgG1
- Top Product
- Discover our top product SQSTM1 Primary Antibody
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- 应用备注
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Recommended Dilution:
ELISA: 1/10000
WB: 1/500 - 1/2000
IHC: 1/200 - 1/1000
FCM: 1/200 - 1/400 - 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.05 % sodium azide and 0.5 % protein stabilizer
- 储存液
- Sodium azide
- 注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- Store at 4 °C or at -20 °C for long term.
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Accumulation of p62/SQSTM1 is associated with poor prognosis in patients with lung adenocarcinoma." in: Cancer science, Vol. 103, Issue 4, pp. 760-6, (2012) (PubMed).
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Accumulation of p62/SQSTM1 is associated with poor prognosis in patients with lung adenocarcinoma." in: Cancer science, Vol. 103, Issue 4, pp. 760-6, (2012) (PubMed).
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- 抗原
- SQSTM1 (Sequestosome 1 (SQSTM1))
- 别名
- SQSTM1 (SQSTM1 产品)
- 别名
- SQSTM1 antibody, sqstm1 antibody, MGC79491 antibody, A170 antibody, OSIL antibody, PDB3 antibody, ZIP3 antibody, p60 antibody, p62 antibody, p62B antibody, OSF-6 antibody, Osi antibody, STAP antibody, ZIP antibody, sb:cb621 antibody, zgc:85784 antibody, sequestosome 1 antibody, sequestosome 1 L homeolog antibody, SQSTM1 antibody, sqstm1 antibody, Sqstm1 antibody, sqstm1.L antibody
- 背景
- This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone.
- 分子量
- 47.7 kDa
- 基因ID
- 8878
- HGNC
- 8878
- 途径
- NF-kappaB Signaling, Neurotrophin Signaling Pathway, Autophagy
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