储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0051R
特异性： Endogenous
基因名称： SQSTM1 ORCA OSIL
蛋白名称： SQSTM
Organism-1： Human
基因ID-1： 8878
SwissProt-1： Q13501
Organism-2： Mouse
基因ID-2： 18412
SwissProt-2： Q64337
Organism-3： Rat
基因ID-3： 113894
SwissProt-3： O08623
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. [provided by RefSeq, Mar 2009],
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0051R
特异性： Endogenous
基因名称： SQSTM1 ORCA OSIL
蛋白名称： SQSTM
Organism-1： Human
基因ID-1： 8878
SwissProt-1： Q13501
Organism-2： Mouse
基因ID-2： 18412
SwissProt-2： Q64337
Organism-3： Rat
基因ID-3： 113894
SwissProt-3： O08623
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. [provided by RefSeq, Mar 2009],
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