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DNA修復(fù)蛋白NBS1抗體

  • 更新時(shí)間:  2023-09-05
  • 產(chǎn)品型號:  
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  • DNA修復(fù)蛋白NBS1抗體別 名:p95 NBS1; Nijmegen breakage syndrome 1; Nijmegen breakage syndrome 1 (nibrin); AT V1; AT V2; AT-V1; AT-V2; ATV; Cell cycle regulatory protein p95; NBS 1; NBS; NBS1; Nibrin; Nijmege
詳細(xì)介紹

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(yàn)、研究實(shí)驗(yàn)、教學(xué)實(shí)驗(yàn)、化學(xué)配方使用的純凈化學(xué)品,價(jià)格實(shí)惠,多種規(guī)格供應(yīng),售后完善。
英文名稱: NBN

中文名稱: DNA修復(fù)蛋白NBS1抗體

規(guī)格:50ul、100ul、200ul
   :p95 NBS1; Nijmegen breakage syndrome 1; Nijmegen breakage syndrome 1 (nibrin); AT V1; AT V2; AT-V1; AT-V2; ATV; Cell cycle regulatory protein p95; NBS 1; NBS; NBS1; Nibrin; Nijmegen breakage syndrome; Nijmegen breakage syndrome protein 1; p95; NBN_HUMAN; Nijmegen breakage syndrome protein 1.

研究領(lǐng)域:腫瘤  細(xì)胞生物  免疫學(xué)  染色質(zhì)和核信號  信號轉(zhuǎn)導(dǎo)  轉(zhuǎn)錄調(diào)節(jié)因子

抗體來源:Rabbit

克隆類型:Polyclonal

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

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=1:100-500 (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:85kDa

細(xì)胞定位:細(xì)胞核

   :Liquid

   :1mg/ml

:KLH conjugated synthetic peptide derived from human NBS1: 651-754/754

   :IgG

純化方法:affinity purified by Protein A

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

保存條件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

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

產(chǎn)品介紹:Component of the MRE11/RAD50/NBN (MRN complex) which plays a critical role in the cellular response to DNA damage and the maintenance of chromosome integrity. The complex is involved in double-strand break (DSB) repair, DNA recombination, maintenance of telomere integrity, cell cycle checkpoint control and meiosis. The complex possesses single-strand endonuclease activity and double-strand-specific 3'-5' exonuclease activity, which are provided by MRE11A. RAD50 may be required to bind DNA ends and hold them in close proximity. NBN modulate the DNA damage signal sensing by recruiting PI3/PI4-kinase family members ATM, ATR, and probably DNA-PKcs to the DNA damage sites and activating their functions. It can also recruit MRE11 and RAD50 to the proximity of DSBs by an interaction with the histone H2AX. NBN also functions in telomere length maintenance by generating the 3' overhang which serves as a primer for telomerase dependent telomere elongation. NBN is a major player in the control of intra-S-phase checkpoint and there is some evidence that NBN is involved in G1 and G2 checkpoints. The roles of NBS1/MRN encompass DNA damage sensor, signal transducer, and effector, which enable cells to maintain DNA integrity and genomic stability.

Function:

Component of the MRE11-RAD50-NBN (MRN complex) which plays a critical role in the cellular response to DNA damage and the maintenance of chromosome integrity. The complex is involved in double-strand break (DSB) repair, DNA recombination, maintenance of telomere integrity, cell cycle checkpoint control and meiosis. The complex possesses single-strand endonuclease activity and double-strand-specific 3'-5' exonuclease activity, which are provided by MRE11A. RAD50 may be required to bind DNA ends and hold them in close proximity. NBN modulate the DNA damage signal sensing by recruiting PI3/PI4-kinase family members ATM, ATR, and probably DNA-PKcs to the DNA damage sites and activating their functions. It can also recruit MRE11 and RAD50 to the proximity of DSBs by an interaction with the histone H2AX. NBN also functions in telomere length maintenance by generating the 3' overhang which serves as a primer for telomerase dependent telomere elongation. NBN is a major player in the control of intra-S-phase checkpoint and there is some evidence that NBN is involved in G1 and G2 checkpoints. The roles of NBS1/MRN encompass DNA damage sensor, signal transducer, and effector, which enable cells to maintain DNA integrity and genomic stability. Forms a complex with RBBP8 to link DNA double-strand break sensing to resection.
抗體基本結(jié)構(gòu):

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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(shí)驗(yàn)動物 兔

 e.其它材料及試劑

2、選擇實(shí)驗(yàn)活體。

3、進(jìn)行動物免疫實(shí)驗(yàn)。

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(shí)驗(yàn)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)

免疫熒光技術(shù)的實(shí)驗(yàn)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(shí)驗(yàn)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(shí)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。

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(jià)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。

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