PE Mouse Anti-Human CD335 (NKp46)
產(chǎn)品名稱: PE Mouse Anti-Human CD335 (NKp46)
產(chǎn)品型號(hào): BD-557991
產(chǎn)品展商: BD Pharmingen
產(chǎn)品文檔: 無(wú)相關(guān)文檔
簡(jiǎn)單介紹
上海創(chuàng)賽優(yōu)勢(shì)提供PE Mouse Anti-Human CD335 (NKp46)，BD抗體現(xiàn)貨促銷PE Mouse Anti-Human CD335 (NKp46)，BD抗體優(yōu)惠促銷PE Mouse Anti-Human CD335 (NKp46)，歡迎來(lái)電咨詢：400-608-7598.
PE Mouse Anti-Human CD335 (NKp46)
的詳細(xì)介紹
產(chǎn)品名稱:PE 小鼠抗人 CD335 (NKp46) 抗體；PE Mouse Anti-Human CD335 (NKp46)
中文名稱:PE 小鼠抗人 CD335 (NKp46) 抗體
英文名稱:PE Mouse Anti-Human CD335 (NKp46)
PE Mouse Anti-Human CD335 (NKp46) 產(chǎn)品介紹：
Material Number: 557991
Alternate Name: NCR1; NK-p46; hNKp46; LY94; Natural cytotoxicity triggering receptor 1
Size: 100 tests
Vol. per Test: 20 μl
Concentration: Optimal
Clone: 9E2/Nkp46
Immunogen: Human NKp46 Recombinant Protein
Isotype: Mouse (BALB/c) IgG1, κ
Reactivity: QC Testing: Human
Storage Buffer: Aqueous buffered solution containing BSA and ≤0.09% sodium azide.
PE Mouse Anti-Human CD335 (NKp46) Description：
The 9E2/Nkp46 monoclonal antibody specifically binds to CD335. CD335 is also known as the Natural killer cell p46-related protein
(NKp46) and the Natural cytotoxicity triggering receptor 1 (NCR1). CD335 is a 46 kDa type I membrane glycoprotein that is expressed on
resting and activated NK cells. Its extracellular region contains two C2-type, Ig-like domains. The transmembrane domain contains a
positively charged amino acid (Arg) which could be involved in stabilizing the association with CD3ζ. Its intracellular region does not contain
immunoreceptor tyrosine-based activating motifs (ITAM), but it is linked to intracytoplasmic transduction machinery by its association with
CD3ζ and FcεRIγ adaptor proteins. CD335 along with NKp30 and NKp44 are referred to as natural cytotoxicity receptors (NCR). These
receptors play very important roles in cells that kill virus-infected target cells, tumor cells and MHC-class I-unprotected cells.
PE Mouse Anti-Human CD335 (NKp46) Preparation and Storage：
Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.
The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.
The antibody was conjugated with R-PE under optimum conditions, and unconjugated antibody and free PE were removed.
