商品詳情：
英文名稱(chēng)：TERT

別    名:EST2; hEST2; TCS1; Telomerase associated protein 2; Telomerase Catalytic Subunit; Telomere Reverse Transcriptase; Telomerase reverse transcriptase; TERT; TP2; TRT; TERT_HUMAN; Telomerase reverse transcriptase; HEST2; Telomerase catalytic subunit; Telomerase-associated protein 2.

研究領(lǐng)域:腫瘤  細胞生物  免疫學(xué)  細胞凋亡  轉錄調節因子

抗體來(lái)源:Rabbit

克隆類(lèi)型:Polyclonal

交叉反應:Human, Mouse,  (predicted: Rat, Dog, )

產(chǎn)品應用:WB=1:500-2000 ELISA=1:5000-10000 Flow-Cyt=1μg/Test ICC=1:100

not yet tested in other applications.

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

理論分子量:124kDa

細胞定位:細胞核 細胞漿

性    狀:Liquid

濃    度:1mg/ml

免 疫 原:KLH conjugated synthetic peptide derived from human TERT: 521-620/1132

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:Telomerase is a ribonucleoprotein enzyme essential for the replication of chromosome termini in most eukaryotes. It elongates telomeres. It is a reverse transcriptase that adds simple sequence repeats to chromosome ends by copying a template sequence within the RNA component of the enzyme. Telomerase are large DNA-protein complexes with telomerase expression being the subject of recent research due to its link to cell immortalization. Recent evidence has shown that MYC upregulates the catalytic subunit of telomerase, TERT, and that Telomerase is a ribonucleoprotein polymerase that maintains telomere ends by addition of the telomere repeat TTAGGG. The enzyme consists of a protein component with reverse transcriptase activity, encoded by this gene, and an RNA component which serves as a template for the telomere repeat. Telomerase expression plays a role in cellular senescence, as it is normally repressed in postnatal somatic cells resulting in progressive shortening of telomeres. Deregulation of telomerase expression in somatic cells may be involved in oncogenesis. Studies in mouse suggest that telomerase also participates in chromosomal repair, since de novo synthesis of telomere repeats may occur at double-stranded breaks. Alternatively spliced variants encoding different isoforms of telomerase reverse transcriptase have been identified; the full-length sequence of some variants has not been determined. Alternative splicing at this locus is thought to be one mechanism of regulation of telomerase activity. [provided by RefSeq, Jul 2008].

Telomerase is a ribonucleoprotein enzyme essential for the replication of chromosome termini in most eukaryotes. Active in progenitor and cancer cells. Inactive, or very low activity, in normal somatic cells. Catalytic component of the teleromerase holoenzyme complex whose main activity is the elongation of telomeres by acting as a reverse transcriptase that adds simple sequence repeats to chromosome ends by copying a template sequence within the RNA component of the enzyme. Catalyzes the RNA-dependent extension of 3'-chromosomal termini with the 6-nucleotide telomeric repeat unit, 5'-TTAGGG-3'. The catalytic cycle involves primer binding, primer extension and release of product once the template boundary has been reached or nascent product translocation followed by further extension. More active on substrates containing 2 or 3 telomeric repeats. Telomerase activity is regulated by a number of factors including telomerase complex-associated proteins, chaperones and polypeptide modifiers. Modulates Wnt signaling. Plays important roles in aging and antiapoptosis.

商品屬性：

實(shí)驗原理 :

（1）公司產(chǎn)品僅用于科研特異性結合抗原：抗體本身不能直接溶解或殺傷帶有特異抗原的靶細胞，通常需要補體或吞噬細胞等共同發(fā)揮效應以清除病原微生物或導致病理?yè)p傷。然而，抗體可通過(guò)與病毒或毒素的特異性結合，直接發(fā)揮中和病毒的作用。

（2）活補體：IgM、IgG1、IgG2和IgG3可通過(guò)經(jīng)典途徑激活補體，凝聚的IgA、IgG4和IgE可通過(guò)替代途徑激活補體。

（3）結合細胞：不同類(lèi)別的免疫球蛋白，可結合不同種的細胞，參與免疫應答。

（4）可通過(guò)胎盤(pán)及粘膜：免疫球蛋白G（IgG）能通過(guò)胎盤(pán)進(jìn)入胎兒血流中，使胎兒形成自然被動(dòng)免疫。免疫球蛋白A（IgA）可通過(guò)消化道及呼吸道粘膜，是粘膜局部抗感染免疫的主要因素。

（5）具有抗原性：抗體分子是一種蛋白質(zhì)，也具有刺機體產(chǎn)生免疫應答的性能。不同的免疫球蛋白分子，各具有不同的抗原性。

（6）抗體對理化因子的抵抗力與一般球蛋白相同：不耐熱，60～70℃即被破壞。各種酶及能使蛋白質(zhì)凝固變性的物質(zhì)，均能破壞抗體的作用?？贵w可被中性鹽類(lèi)沉淀。在生產(chǎn)上?？捎昧蛩徜@或硫酸鈉從免疫血清中沉淀出含有抗體的球蛋白，再經(jīng)透析法將其純化。

一抗和二抗的區別：

第一抗體就是平常所說(shuō)的抗體，即能和抗原特異性結合。

第二抗體是能和抗體結合的，即抗體的抗體。主要用于檢測抗體的存在。

一抗是針對抗原的抗體，二抗是針對一抗的抗體。即抗體也可以充當抗原刺激機體產(chǎn)生抗體。也就是說(shuō)，抗原進(jìn)入機體刺激機體免疫系統產(chǎn)生免疫應答，由B細胞可以產(chǎn)生與相應抗原發(fā)生特異性結合的特殊蛋白質(zhì)。

一抗二抗都是一種可以特異結合別的物質(zhì)的基團，而且一抗可以至少結合兩種其他基團（底物和二抗）。

一抗：可以特異結合底物，就是識別出我們想要檢測的東西。一抗和底物結合與否用肉眼是看不出來(lái)的。

二抗：可以和一抗結合，并帶有可以被檢測出的標記(如帶熒光、放射性、化學(xué)發(fā)光或顯色基團），作用是檢測一抗。 如果一抗自己帶有可以被檢測出的標記(如帶熒光、放射性、化學(xué)發(fā)光或顯色基團），則不需要二抗。但這樣成本很高，因為一種一抗只識別一種底物。所以如今的設計一般是二抗帶上可檢測標記，再來(lái)檢測一抗。而一抗識別底物。這樣，當一抗結合到底物上，就可以通過(guò)二抗檢測出來(lái)。
抗體的標記實(shí)驗要點(diǎn)：

1.如在反應混合液中有疊氮鈉或游離氨基存在,會(huì )抑制標記反應。因此,蛋白質(zhì)在反應前要對 0.1mol/L緩沖液或0.5mol/L硼酸緩沖液充分透析；

2.所用的NHSB及待化蛋白質(zhì)之間的分子比按蛋白質(zhì)表面的ε-氨基的密度會(huì )有所不同,選擇不當則影響標記的效率,應先用幾個(gè)不同的分子比來(lái)篩選最適條件；

3.用NHSB量過(guò)量也是不利的,抗原的結合位點(diǎn)可能因此被封閉,導致抗體失活；

4.由于抗體的氨基不易接近可能造成化不足,此時(shí)可加入去污劑如 Triton x-100, Tween20等；

5.當游離ε-氨基(賴(lài)氨酸殘基的氨基)存在于抗體的抗原結合位點(diǎn)時(shí),或位于酶的催化位點(diǎn)時(shí),化會(huì )降低或損傷抗體蛋白的結合力或活性；

6.還可能與不同的功能基團,如羰基、氨基、巰基、異咪唑基及基,也可與糖基共價(jià)結合；

7.交聯(lián)反應后,應充分透析,否則,殘余的會(huì )對化抗體與親和素的結合產(chǎn)生競爭作用；

8.在細胞的熒光標記實(shí)驗中,中和親和素的本底低,但由于鏈霉親和素含有少量正電荷,故對某些細胞可導致高本底。

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