上海研盟生物科技有限公司Anti-RPLP0抗體*,主要應(yīng)用于WB、IHC、IF、ELISA、流式細(xì)胞術(shù)等實(shí)驗(yàn)中。說明書隨貨發(fā)送,您也可以直接我司在線客服索取??头?/span>
英文名稱:Anti-RPLP0 antibody
中文名稱:酸性核糖體磷蛋白大亞基P0抗體
酸性核糖體磷蛋白大亞基P0抗體保存條件:Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
酸性核糖體磷蛋白大亞基P0抗體,Anti-RPLP0抗體抗原修復(fù)方法:
方法1:沸水浴修復(fù),將盛有修復(fù)液和玻片的燒杯置于沸水浴環(huán)境,保持外部沸騰狀態(tài)15min,自然冷卻至室溫。
方法2:微波修復(fù),將盛有修復(fù)液和玻片的燒杯置于微波爐中,高火5min,停火3min,中火5min,自然冷卻至室溫。
方法3:高壓修復(fù),修復(fù)液加入高壓鍋加熱至沸騰,放入玻片,封蓋加壓持續(xù)加熱至噴氣時(shí)開始計(jì)時(shí)修復(fù)2min,自然冷卻至室溫。
方法4:使用*修復(fù),將*修復(fù)液加入到組織上,37℃,消化30min
★研盟生物★酸性核糖體磷蛋白大亞基P0抗體,Anti-RPLP0抗體
實(shí)驗(yàn)注意事項(xiàng):
1、 把聚丙烯酰胺凝膠中的蛋白質(zhì)電泳轉(zhuǎn)移到硝酸纖維膜上;
a. 轉(zhuǎn)移緩沖液洗滌凝膠和硝酸纖維素膜,將硝酸纖維素膜鋪在凝膠上,用5ml移液管在凝膠上來回滾動(dòng)去除所有的氣泡
b. 在凝膠/濾膜外再包一張3mm濾紙(預(yù)先用轉(zhuǎn)移緩沖液浸濕),將凝膠夾在中間,保持濕潤和沒有氣泡
c. 將此濾紙/凝膠/薄膜濾紙按照廠家建議方法放入電泳裝置中,凝膠面向陰極
d. 將上述裝置放入緩沖液槽中,并灌滿轉(zhuǎn)移緩沖液以淹沒凝膠
e. 按照廠家所示接通電源開始電泳轉(zhuǎn)移
f. 轉(zhuǎn)移結(jié)束后,取出薄膜和凝膠,棄去凝膠
2、 將薄膜漂在氨基黑中快速染色,直至分子量標(biāo)準(zhǔn)顯現(xiàn)時(shí)取出,記錄下標(biāo)準(zhǔn)位置;
3、 用100ml水洗滌纖維素膜,必要時(shí)可用脫色緩沖液;
4、 膜置印跡緩沖液中于37℃保溫1小時(shí);
5、 室溫下,用PBS-Tween緩沖液洗滌薄膜
6、 用封口機(jī)將薄膜封入塑料袋中,盡可能不留空氣;
7、 袋的一角剪一緩沖液的小口,用透析袋夾緊;
8、 混合:NGS(100微升),印跡緩沖液中的抗體(2.5-5毫升),加在裝薄膜的袋中,于室溫下?lián)u動(dòng)2小時(shí)(或4℃過ye);
9、 用總體積300ml PBS-Tween緩沖液,分4次在一淺盤中洗滌薄膜,每次75ml;
10、將連接*的羊抗兔IgG(40微升溶于10毫升印跡緩沖液/100微升 NGS)加在袋內(nèi),于室溫下?lián)u動(dòng)1小時(shí);
11、按步驟9洗滌;
12、加入抗生素蛋白-HRP(40微升溶于10毫升印跡緩沖液/100微升 NGS),于室溫下?lián)u動(dòng);
13、Western Blot中轉(zhuǎn)移在膜上的蛋白處于變性狀態(tài),空間結(jié)構(gòu)改變,因此那些識(shí)別空間表位的抗體不能用于Western Blot檢測(cè)。這種情況可以將表達(dá)目的蛋白的細(xì)胞或細(xì)胞裂解液中的所有蛋白物素化,再用酶標(biāo)記親和素進(jìn)行Western Blot。實(shí)驗(yàn)中取膠和膜需帶手套。
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相關(guān)標(biāo)記抗體:HRP標(biāo)記抗體,Biotin標(biāo)記抗體,Gold標(biāo)記抗體,RBITC標(biāo)記抗體,AP標(biāo)記抗體,FITC標(biāo)記抗體,Cy3標(biāo)記抗體,Cy5標(biāo)記抗體,Cy5.5標(biāo)記抗體,Cy7標(biāo)記抗體,PE標(biāo)記抗體,PE-Cy3標(biāo)記抗體,PE-Cy5標(biāo)記抗體,PE-Cy5.5標(biāo)記抗體,PE-Cy7標(biāo)記抗體,APC標(biāo)記抗體,Alexa Fluor 350標(biāo)記抗體,Alexa Fluor 488標(biāo)記抗體,Alexa Fluor 555標(biāo)記抗體,Alexa Fluor 647標(biāo)記抗體
簡(jiǎn)單介紹:
產(chǎn)品別名:36B4; 60S acidic ribosomal protein P0; 60S ribosomal protein L10E; Acidic ribosomal phosphoprotein P0; Arbp; L10E; LP0; MGC107165; MGC107166; MGC111226; MGC88175; OTTMUSP00000015585; P0; PRLP0; Ribosomal protein P0; Ribosomal protein, large, P0; RLA0_HUMAN; rplP0; RPP0.
抗體來源:Rabbit or Mouse
保質(zhì)期:1年
克隆類型:Polyclonal or monoclonal
性 狀:Lyophilized or Liquid
濃 度:1mg/1ml
背景介紹:Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximay 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein, which is the functional equivalent of the E. coli L10 ribosomal protein, belongs to the L10P family of ribosomal proteins. It is a neutral phosphoprotein with a C-terminal end that is nearly identical to the C-terminal ends of the acidic ribosomal phosphoproteins P1 and P2. The P0 protein can interact with P1 and P2 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. Transcript variants derived from alternative splicing exist; they encode the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.
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