RNA聚合酶II抗體

抗體制備過程：

1.材料與試劑

 a．提取的動物 Ig

 b．弗氏佐劑和弗氏不佐劑

 d．實驗動物 兔

 e．其它材料及試劑

2、選擇實驗活體。

3、進(jìn)行動物免疫實驗。

4、試取血樣進(jìn)行測試，查看免疫效果。

5、如果免疫成功，殺死實驗活體，采集全部血清。

6、純化出抗體。

7、鑒定抗體。胎牛血清（無菌采制）

公司產(chǎn)品僅用于科研專業(yè)供應(yīng)的抗體，是用于化學(xué)反應(yīng)、分析化驗、研究實驗、教學(xué)實驗、化學(xué)配方使用的純凈化學(xué)品，價格實惠，多種規(guī)格供應(yīng)，售后*。
英文名稱: RNA polymerase II

中文名稱: RNA聚合酶II抗體

規(guī)格：50ul、100ul、200ul
別    名:POLR2A; POLR2; DNA directed RNA polymerase II A; DNA-directed RNA polymerase II largest subunit; DNA-directed RNA polymerase II subunit A; RPB1_HUMAN.

研究領(lǐng)域:染色質(zhì)和核信號  轉(zhuǎn)錄調(diào)節(jié)因子  表觀遺傳學(xué)

抗體來源:Rabbit

克隆類型:Polyclonal

交叉反應(yīng):Mouse, Rat,  (predicted: Human, Dog, Pig, Cow, Horse, )

產(chǎn)品應(yīng)用:WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 （石蠟切片需做抗原修復(fù)）

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

理論分子量:217kDa

細(xì)胞定位:細(xì)胞核

性    狀:Liquid

濃    度:1mg/ml

免 疫 原:KLH conjugated synthetic peptide derived from human Pol II/RNA polymerase II: 101-200/1970

亞    型:IgG

純化方法:affinity purified by Protein A

緩 沖 液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

注意事項:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

產(chǎn)品介紹:RNA polymerase II (Pol II) is an enzyme that is composed of twelve subunits and is responsible for the transcription of protein-coding genes. Transcription initiation requires Pol II-mediated recruitment of transcription machinery to a target promoter, thereby allowing transcription to begin. The largest subunit of Pol II (referred to as RPB1 or RPB205) is a 1,840 amino acid protein that contains one C2H2-type zinc finger and a C-terminal domain comprised of several heptapeptide repeats. Although Pol II function requires the cooperation of all twelve subunits, the largest subunit conveys Pol II catalytic activity and, together with the second largest subunit, forms the active center of the Pol II enzyme. Additionally, the large subunit participates in forming the DNA-binding domain of Pol II, a groove that is necessary for transcription of the DNA template. Without proper function of the large subunit, mRNA synthesis and subsequent transcription elongation cannot occur.

DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates. Largest and catalytic component of RNA polymerase II which synthesizes mRNA precursors and many functional non-coding RNAs. Forms the polymerase active center together with the second largest subunit. Pol II is the central component of the basal RNA polymerase II transcription machinery. It is composed of  elements that move relative to each other. RPB1 is part of the core element with the central large cleft, the clamp element that moves to open and close the cleft and the jaws that are thought to grab the incoming DNA template. At the start of transcription, a single stranded DNA template strand of the promoter is positioned within the central active site cleft of Pol II. A bridging helix emanates from RPB1 and crosses the cleft near the catalytic site and is thought to promote translocation of Pol II by acting as a ratchet that moves the RNA-DNA hybrid through the active site by switching from straight to bent conformations at each step of nucleotide addition. During transcription elongation, Pol II moves on the template as the transcript elongates. Elongation is influenced by the phosphorylation status of the C-terminal domain (CTD) of Pol II largest subunit (RPB1), which serves as a platform for assembly of factors that regulate transcription initiation, elongation, termination and mRNA processing. Acts as a RNA-dependent RNA polymerase when associated with small delta antigen of Hepatitis delta virus, acting both as a replicate and transcriptase for the viral RNA circular genome.
抗體基本結(jié)構(gòu)：

免疫熒光技術(shù)的實驗步驟：

一、準(zhǔn)備好試劑與儀器：

磷酸鹽緩沖鹽水、熒光標(biāo)記的抗體溶液、緩沖甘油、搪瓷桶三只、有蓋搪瓷盒一只、熒光顯微鏡、玻片架、濾紙、37℃溫箱等。

二、實驗步驟

1.滴加0.01mol/L，pH7.4的PBS于待檢標(biāo)本片上，十分鐘后棄去，使標(biāo)本保持一定濕度。

2.滴加適當(dāng)稀釋的熒光標(biāo)記的抗體溶液，使其覆蓋標(biāo)本，置于有蓋搪瓷盒內(nèi)，保溫一定時間以三十分鐘為參考。

3.取出玻片，置玻片架上，先用0.01mol/L，pH7.4的PBS沖洗后，再按順序過0.01mol/L，pH7.4的PBS三缸浸泡，每缸三到五分鐘，并不停地?fù)u晃振蕩。

4.取出玻片，用濾紙吸去多余水分，但不使標(biāo)本干燥，加一滴緩沖甘油，以蓋玻片覆蓋。

5.立即用熒光顯微鏡觀察。觀察標(biāo)本的特異性熒光強(qiáng)度。

公司出售的產(chǎn)品：

抗體的定義：

抗體（antibody），（免疫球蛋白不僅僅只是抗體）是一種由漿細(xì)胞（效應(yīng)B細(xì)胞）分泌，被免疫系統(tǒng)用來鑒別與中和外來物質(zhì)如細(xì)菌、病毒等的大型Y形蛋白質(zhì)，僅被發(fā)現(xiàn)存在于脊椎動物的血液等體液中，及其B細(xì)胞的細(xì)胞膜表面。抗體能識別特定外來物的一個特征，該外來目標(biāo)被稱為抗原。

動物抗體功能分類：

①豬抗體：豬瘟抗體，豬藍(lán)耳抗體，豬圓環(huán)病毒抗體，豬偽狂犬抗體，豬細(xì)小病毒抗體，豬口蹄疫抗體，豬流感抗體等。

②禽抗體:小鵝瘟抗體，鴨肝抗體抗體，鴨漿膜炎抗體，抗體，新城疫抗體等

③牛抗體：牛口蹄疫抗體，奶牛乳房炎抗體，牛流行熱抗體，牛病毒性腹瀉抗體，牛出血性敗血癥抗體等

④羊抗體：羊痘抗體，羊口蹄疫抗體，羊小反芻獸疫抗體，羊快疫抗體，羊腸毒血癥抗體，羊猝疽抗體，羊黑疫抗體等。

⑤犬抗體：犬狂犬病抗體、犬瘟熱抗體、犬副流感抗體、犬腺病毒抗體與犬細(xì)小病毒病抗體，狐貉水貂的偽狂犬抗體、細(xì)小病毒抗體、乙腦抗體等。

抗體的結(jié)構(gòu)：

抗體是具有4條多肽鏈的對稱結(jié)構(gòu)，其中2條較長、相對分子量較大的相同的重鏈(H鏈)；2條較短、相對分子量較小的相同的輕鏈(L鏈)。鏈間由二硫鍵和非共價鍵聯(lián)結(jié)形成一個由4條多肽鏈構(gòu)成的單體分子。輕鏈有κ和λ兩種，重鏈有μ、δ、γ、ε和α五種。 整個抗體分子可分為恒定區(qū)和可變區(qū)兩部分。在給定的物種中，不同抗體分子的恒定區(qū)都具有相同的或幾乎相同的氨基酸序列。可變區(qū)位于"Y"的兩臂末端。在可變區(qū)內(nèi)有一小部分氨基酸殘基變化特別強(qiáng)烈，這些氨基酸的殘基組成和排列順序更易發(fā)生變異區(qū)域稱高變區(qū)。高變區(qū)位于分子表面，最多由17個氨基酸殘基構(gòu)成，少則只有2 ～ 3個。高變區(qū)氨基酸序列決定了該抗體結(jié)合抗原抗原的特異性。一個抗體分子上的兩個抗原結(jié)合部位是相同的，位于兩臂末端稱抗原結(jié)合片段(antigen-binding fragment, Fab)。"Y"的柄部稱結(jié)晶片段(crystalline fragment,FC)，糖結(jié)合在FC 上。