SML2967
Gp91ds-tat, scrambled trifluoroacetate
≥95% (HPLC)
别名:
Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Cys-Leu-Arg-Ile-Thr-Arg-Gln-Ser-Arg-NH2 trifluoroacetate, Gp91 ds-tat, scrambled trifluoroacetate, NADPH oxidase 2 docking sequence-tat trifluoroacetate, NOX2 ds-tat, scrambled trifluoroacetate, NOX2ds-tat, scrambled trifluoroacetate, RKKRRQRRR-CLRITRQSR-NH2 trifluoroacetate, scrambled Gp91phox docking sequence-tat trifluoroacetate, scrambled NOX2 docking sequence-tat trifluoroacetate
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关于此项目
经验公式（希尔记法）:
C98H190N50O22S · xC2HF3O2
分子量:
2452.94 (free base basis)
NACRES:
NA.77
UNSPSC Code:
12352200
Biochem/physiol Actions
Inactive control peptide for the NADPH oxidase inhibitor peptide gp91ds-tat (NOX2ds-tat). The control peptide is composed of a membrane-permeant HIV-1 Tat protein transduction domain sequence (aa49-57) N-terminal to a scrambled sequence of murine gp91phox (NOX2) aa86-94.
Scrambled inactive control peptide for the NADPH oxidase inhibitor peptide gp91ds-tat (NOX2ds-tat).
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
常规特殊物品
此项目有
F E Rey et al.
Circulation research, 89(5), 408-414 (2001-09-05)
We previously reported enhanced expression of the p67(phox) and gp91(phox) components of NAD(P)H oxidase in angiotensin (Ang) II-induced hypertension, suggesting de novo assembly in response to Ang II. To examine the direct involvement of NAD(P)H oxidases in Ang II-induced O(2)(-)
Dina Vara et al.
Haematologica, 104(9), 1879-1891 (2019-01-27)
The regulation of platelets by oxidants is critical for vascular health and may explain thrombotic complications in diseases such as diabetes and dementia, but remains poorly understood. Here, we describe a novel technique combining electron paramagnetic resonance spectroscopy and turbidimetry
Boris Sabirzhanov et al.
Brain, behavior, and immunity, 80, 73-87 (2019-02-27)
NADPH oxidase (NOX2) is an enzyme that induces reactive oxygen species (ROS) and serves as a switch between the pro-inflammatory and neurorestorative microglial/macrophage phenotypes; such changes play an important role in neuropathic pain and motor dysfunction. Increased NOX2 expression after
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