上海研盟生物科技有限公司Anti-HDX抗體*,主要應(yīng)用于WB、IHC、IF、ELISA、流式細(xì)胞術(shù)等實驗中。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-HDX antibody
中文名稱:高度發(fā)散同源異型盒蛋白抗體
高度發(fā)散同源異型盒蛋白抗體保存條件: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.
高度發(fā)散同源異型盒蛋白抗體,Anti-HDX抗體抗原的分類:
一. 免疫學(xué)分類:
(1)*抗原、半抗原;
(2)胸腺依賴抗原與非依賴抗原。
二. 臨床分類:
(1)外源性抗原:微生物、花粉等;
(2)內(nèi)源性抗原:隱蔽的自身抗原、腫瘤相關(guān)抗原等;
(3)同種異型抗原:人類白細(xì)胞抗原、血型抗原;
(4)異嗜性抗原:人與其他動物、植物等之間存在的共同抗原。
★研盟生物★高度發(fā)散同源異型盒蛋白抗體,Anti-HDX抗體
Western Blotting 實驗步驟概述
1、 組織取材:組織塊稱重
2、 利用液氮、研缽粉碎組織塊
3、 加入RIPA緩沖液(每克組織3ml RIPA),PMSF(每克組織30μl,10 mg/ml PMSF),
利用Polytron進(jìn)一步勻漿(15,000轉(zhuǎn)/分*1分鐘)維持4℃
4、 加入PMSF(每克組織30μl,10 mg/ml PMSF),冰上孵育30分鐘
5、 移入離心管4℃,約20,000g(約15,000轉(zhuǎn))15分鐘
6、 上清液為細(xì)胞裂解液可分裝-20℃保存
7、 進(jìn)行Bradford比色法測定蛋白質(zhì)濃度
8、 取相同質(zhì)量的細(xì)胞裂解液(體積*蛋白質(zhì)濃度),并加等體積的2×電泳加樣緩沖液
9、 沸水浴中3分鐘
10、上樣
11、電泳(濃縮膠20mA,分離膠35mA)
12、電轉(zhuǎn)膜儀轉(zhuǎn)膜(100mA 40分鐘)
13、膜用麗春紅染色,膠用考馬斯亮藍(lán)染色
14、Westernblot 試劑盒顯色
15、分析比較記錄
★研盟生物 ★合作: ★客服
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
簡單介紹:
產(chǎn)品別名:CXorf43; D030011N01Rik; FLJ30678; Hdx; HDX_HUMAN; Highly divergent homeobox; MGC126769; MGC126771; OTTHUMP00000062139.
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:HDX (highly divergent homeobox) is a 690 amino acid nuclear protein that contains two homeobox DNA-binding domains. Existing as two alternatively spliced isoforms, the gene encoding HDX maps to the human X chromosome, which consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome leads to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
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