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NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
polyclonal
Application:
ELISA, IF, IHC, WB
Species reactivity:
human
Citations:
11
Technique(s):
ELISA: 1:20000, immunofluorescence: 1:100-1:500, immunohistochemistry: 1:50-1:100, western blot: 1:500-1:1000
Uniprot accession no.:
biological source
rabbit
conjugate
unconjugated
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
antigen 131 kDa
species reactivity
human
concentration
~1 mg/mL
technique(s)
ELISA: 1:20000, immunofluorescence: 1:100-1:500, immunohistochemistry: 1:50-1:100, western blot: 1:500-1:1000
NCBI accession no.
UniProt accession no.
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
Gene Information
human ... NOS2(4843)
Physical form
兔IgG,溶于磷酸盐缓冲液(不含Mg2+和Ca2+),pH 7.4,150mM NaCl,0.02%叠氮化钠和50%甘油中。
Application
兔抗INOS,C端抗体可用于免疫印迹。
Biochem/physiol Actions
在感染、组织损伤和炎症期间观察到INOS(诱导型一氧化氮合酶)的上调。INOS负责产生NO(一氧化氮),通过诱导血管舒张来控制血流。NO充当神经递质,可以促进免疫反应。NO还可以响应氧化应激、缺氧、炎性细胞因子(TNF-α,IL-1β,IFN-γ)和脂多糖内毒素而产生抗血栓形成和抗炎作用。iNOS比神经元和内皮NOS产生更多的NO。与这两种同工型不同,iNOS与钙无关。INOS可能与2型糖尿病有关。
Disclaimer
除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。
Features and Benefits
完放心地使用我们的抗体。如果抗体在您的申请的研究中不起作用,我们将全额退款或安排替代抗体。了解更多信息。
General description
INOS(诱导型一氧化氮合酶)基因定位于人类染色体17q11.2。
抗-INOS抗体可检测内源性总INOS蛋白水平。
Immunogen
该抗血清是针对衍生自人iNOS的合成肽而生成的。
免疫原范围: 1101-1150
免疫原范围: 1101-1150
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存储类别
10 - Combustible liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
常规特殊物品
此项目有
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Journal of neuroimmunology, 313, 161-175 (2017-11-18)
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Diagnostics (Basel, Switzerland), 10(5) (2020-05-01)
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Laryngeal squamous cell carcinoma (LSCC) is an aggressive malignancy which lacks early predictors of prognosis. Here, we hypothesized that expression and prognostic characterization of the critical mediators of epithelial to mesenchymal transition (EMT) may provide key information in this regard.
R A Lea et al.
American journal of medical genetics, 105(1), 110-113 (2001-06-27)
Migraine is a debilitating disorder affecting approximately 12% of Caucasian populations. The disease has a large genetic component, although at present the type and number of genes involved is unclear. Candidate gene studies may be useful strategies for identifying genes
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