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由来生物
mouse
品質水準
結合体
unconjugated
抗体製品の状態
ascites fluid
抗体製品タイプ
primary antibodies
クローン
NOS-IN, monoclonal
分子量
antigen 130 kDa
含みます
15 mM sodium azide
化学種の反応性
mouse, rat
包装
antibody small pack of 25 μL
テクニック
microarray: suitable
western blot: 1:1,000 using whole cell extract of the murine macrophage cell line RAW 264.7 activated with LPS and IFN-γ
アイソタイプ
IgG1
UniProtアクセッション番号
輸送温度
dry ice
保管温度
−20°C
ターゲットの翻訳後修飾
unmodified
遺伝子情報
human ... NOS2(4843)
mouse ... Nos2(18126)
rat ... Nos2(24599)
関連するカテゴリー
詳細
Monoclonal Anti-Nitric Oxide Synthase, Inducible (iNOS) (mouse IgG1 isotype) is derived from the NOS-IN hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized BALB/c mouse. Nitric oxide synthase (NOS) is classified into three types based on molecular mass, subcellular location, and Ca2+ dependence. Type I NOS (150-160 kDa) is found in neurons. It is also called as NOS-1, neuronal NOS (nNOS), brain NOS (bNOS), cerebral NOS, constitutive NOS or Ca2+-regulated NOS (cNOS). Type II (130 kDa), best characterized in macrophages, also known as macrophage NOS (mNOS) or inducible NOS (iNOS). Type III (135 kDa) is found in endothelial cells. It is called as endothelial NOS (eNOS, or ecNOS). Type II NOS is Ca2+ -independent and is expressed in activated macrophages and some glial cells after stimulation. iNOS is also found in several other cell types including hepatocytes, chondrocytes, endothelial cells and fibroblasts.
特異性
Monoclonal Anti-Nitric Oxide Synthase, Inducible (iNOS), antibody reacts specifically with inducible-type nitricoxide synthase (iNOS, also termed macNOS and mNOS). It does not react with NOS derived from brain.
免疫原
マウスマクロファ-ジ由来NOシンタ-ゼ(iNOSまたはmacNOS)のアミノ酸1126-1144に相当する合成ペプチドのKLH結合体。免疫原の配列はラットiNOSで高度に保存されていますが、ヒトiNOSとは異なっています。
アプリケーション
Monoclonal Anti-Nitric Oxide Synthase, Inducible (iNOS) has been used in
- immunofluorescence staining
- immunogold electron microscopy
- immunoblotting
- immunohistochemistry
- immunocytochemistry
- enzyme linked immunosorbent assay (ELISA)
生物化学的/生理学的作用
Nitric oxide synthase (NOS) is an enzyme involved in the synthesis of nitric oxide (NO), a free radical generated under physiological conditions by virtually all mammalian cells. NO is formed from arginine by NOS which oxidizes a guanidino nitrogen of arginine, releasing NO and citrulline. NO is a messenger molecule mediating diverse functions including vasodilatation, neurotransmission, and antimicrobial and anti-tumor activities. Various types of NOS may serve a variety of diverse biological pathways.
免責事項
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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保管分類コード
12 - Non Combustible Liquids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
試験成績書(COA)
製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
Involvement of inducible nitric oxide synthase (iNOS) in immune-functioning of Paphia malabarica (Chemnitz, 1782)
Fish & Shellfish Immunology, 84, 384-389 (2019)
Journal of inflammation (London, England), 4, 10-10 (2007-05-08)
Since airway hyperresponsiveness (AHR) and allergic inflammatory changes are regarded as the primary manifestations of asthma, the main goals of asthma treatment are to decrease inflammation and maximize bronchodilation. These goals can be achieved with aerosol therapy. Intravenous administration of
Regulation of boar sperm functionality by the nitric oxide synthase/nitric oxide system
Journal of Assisted Reproduction and Genetics, 1-16 (2019)
Cerebral inducible nitric oxide synthase protein expression in microglia, astrocytes and neurons in Trypanosoma brucei brucei-infected rats
PLoS ONE, 14(4), e0215070-e0215070 (2019)
Effects of nebulized ketamine on allergen-induced airway hyperresponsiveness and inflammation in actively sensitized Brown-Norway rats
Journal of Inflammation, 4(1), 10-10 (2007)
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