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phosphos-PCNA (Tyr211)抗体

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产品名称: phosphos-PCNA (Tyr211)抗体
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产品展商: XYbscience
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简单介绍

phosphos-PCNA (Tyr211)抗体增殖细胞核抗原(PCNA)是与细胞周期相关的一个28kDa的核蛋白,核蛋白对细胞DNA合成的重要。增殖细胞核抗原*初是通过**荧光鉴定为核蛋白,其外观与细胞的增殖状态有关。PCNA是体外复制DNA所必需的,被认为是DNA聚合酶δ的辅助蛋白(辅因子)。phosphos-PCNA (Tyr211)抗体抗增殖细胞核抗原抗体与增殖细胞核的反应。PCNA是细胞DNA合成的基础,也是猿猴病毒40(SV40)DNA体外复制所必需的,它在复制叉中起主导和滞后链合成的作用。PCNA蛋白可能在细胞核中与抗原结构的变化发挥不同的作用。


phosphos-PCNA (Tyr211)抗体  的详细介绍

phosphos-PCNA (Tyr211)抗体特异性结合抗原:抗体本身不能直接溶解或杀伤带有特异抗原的靶细胞,通常需要补体或吞噬细胞等共同发挥效应以**病原微生物或导致病理损伤。然而,抗体可通过与病毒或**的特异性结合,直接发挥中和病毒的作用。

产品编号xy- 2215R

英文名称phosphos-PCNA (Tyr211)

中文名称磷酸化增殖细胞核抗原抗体

别    名PCNA (phospho Y211); p-PCNA (phospho Y211); PCNA(Tyr211); PCNA; Cyclin; DNA polymerase delta auxiliary protein; HGCN8729; MGC8367; Mutagen-sensitive 209 protein; Pcna/cyclin; PCNAR; Polymerase delta accessory protein; Proliferating Cell Nuclear Antigen; PCNA_HUMAN.  

说 明 书100ul  200ul

研究领域细胞生物  细胞凋亡  转录调节因子  细胞类型标志物  

抗体来源Rabbit

克隆类型Polyclonal

phosphos-PCNA (Tyr211)抗体交叉反应 Human, Mouse, Rat, Chicken, Cow, Rabbit, Sheep,

产品应用WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 Flow-Cyt=1μg /test IF=1:100-500 (石蜡切片需做抗原修复)

not yet tested in other applications.

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

分 子 量29kDa

细胞定位细胞核

性    状Lyophilized or Liquid

浓    度1mg/1ml

免 疫 原KLH conjugated Synthesised phosphopeptide derived from human PCNA around the phosphorylation site of Tyr211:LR(p-Y)LN

亚    型IgG

纯化方法affinity purified by Protein A

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

phosphos-PCNA (Tyr211)抗体保存条件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.

PubMedPubMed

产品介绍background:

Proliferating cell nuclear antigen (PCNA) is a 28kDa nuclear protein associated with the cell cycle, a nuclear protein vital for cellular DNA synthesis. Proliferating cell nuclear antigen was originally identified by immunofluorescence as a nuclear protein whose appearance correlated with the proliferate state of the cell. PCNA is required for replication of DNA in vitro and has been identified as the auxiliary protein (cofactor) for DNA polymerase delta. The anti-PCNA antibodies react with the nuclei of proliferating cells. PCNA is essential for cellular DNA synthesis and is also required for the in vitro replication of simian virus 40 (SV40) DNA where it acts to coordinate leading and lagging strand synthesis at the replication fork. The PCNA protein may fulfil several separate roles in the cell nucleus associated with changes in its antigenic structure.


Function:

Auxiliary protein of DNA polymerase delta and is involved in the control of eukaryotic DNA replication by increasing the polymerase's processibility during elongation of the leading strand. Induces a robust stimulatory effect on the 3'-5' exonuclease and 3'-phosphodiesterase, but not apurinic-apyrimidinic (AP) endonuclease, APEX2 activities. Has to be loaded onto DNA in order to be able to stimulate APEX2. Plays a key role in DNA damage response (DDR) by being conveniently positioned at the replication fork to coordinate DNA replication with DNA repair and DNA damage tolerance pathways. Acts as a loading platform to recruit DDR proteins that allow completion of DNA replication after DNA damage and promote postreplication repair: Monoubiquitinated PCNA leads to recruitment of translesion (TLS) polymerases, while 'Lys-63'-linked polyubiquitination of PCNA is involved in error-free pathway and employs recombination mechanisms to synthesize across the lesion.


Subunit:

Homotrimer (By similarity). Forms a complex with activator 1 heteropentamer in the presence of ATP. Interacts with EXO1, POLH, POLK, DNMT1, ERCC5, FEN1, CDC6 and POLDIP2. Interacts with APEX2; this interaction is triggered by reactive oxygen species and increased by misincorporation of uracil in nuclear DNA. Forms a ternary complex with DNTTIP2 and core histone. Interacts with KCTD10 and PPP1R15A (By similarity). Interacts with POLD1, POLD3 and POLD4. Interacts with BAZ1B; the interaction is direct. Interacts with HLTF and SHPRH. Interacts with NUDT15. Interaction is disrupted in response to UV irradiation and acetylation. Interacts with CDKN1A/p21(CIP1) and CDT1; interacts via their PIP-box which also recruits the DCX(DTL) complex. Interacts with DDX11. Interacts with EGFR; positively regulates PCNA. Interacts with PARPBP. Interacts (when ubiquitinated) with SPRTN; leading to enhance RAD18-mediated PCNA ubiquitination. Interacts (when polyubiquitinated) with ZRANB3. Interacts with SMARCAD1. Interacts with CDKN1C. Interacts with KIAA0101/PAF15 (via PIP-box).


Subcellular Location:

Nucleus. Note=Forms nuclear foci representing sites of ongoing DNA replication and vary in morphology and number during S phase. Together with APEX2, is redistributed in discrete nuclear foci in presence of oxidative DNA damaging agents.


Post-translational modifications:

Following DNA damage, can be either monoubiquitinated to stimulate direct bypass of DNA lesions by specialized DNA polymerases or polyubiquitinated to promote recombination-dependent DNA synthesis across DNA lesions by template switching mechanisms. Following induction of replication stress, monoubiquitinated by the UBE2B-RAD18 complex on Lys-164, leading to recruit translesion (TLS) polymerases, which are able to synthesize across DNA lesions in a potentially error-prone manner. An error-free pathway also exists and requires non-canonical polyubiquitination on Lys-164 through 'Lys-63' linkage of ubiquitin moieties by the E2 complex UBE2N-UBE2V2 and the E3 ligases, HLTF, RNF8 and SHPRH. This error-free pathway, also known as template switching, employs recombination mechanisms to synthesize across the lesion, using as a template the undamaged, newly synthesized strand of the sister chromatid. Monoubiquitination at Lys-164 also takes place in undamaged proliferating cells, and is mediated by the DCX(DTL) complex, leading to enhance PCNA-dependent translesion DNA synthesis. Sumoylated during S phase.

Acetylated in response to UV irradiation. Acetylation disrupts interaction with NUDT15 and promotes degradation.

Phosphorylated. Phosphorylation at Tyr-211 by EGFR stabilizes chromatin-associated PCNA.


Similarity:

Belongs to the PCNA family.


SWISS:

P12004


Gene ID:

5111


phosphos-PCNA (Tyr211)抗体antibody, Ab)是由效应B细胞(效应**B细胞)分泌,机体用于抵御外来物质,如病毒,**等抗原,结构呈“Y”字型的球状蛋白质,仅仅存在于脊椎动物的血液和B**细胞膜表面。凡是能够跟抗体结合的物质,均被称作抗原,因此对于抗抗体(能够结合抗体的抗体)来说,抗体本身也是一种抗原物质。

   QQ图片20171030091318

phosphos-PCNA (Tyr211)抗体普通抗体重链和轻链的结构

重链结构:普通的**球蛋白具有2条重链(H链),分子量约为50kD,有μ、δ、γ、ε和α五种重链亚型,对应的**球蛋白名称分别为IgMIgGIgAIgDIgE

轻链结构:  普通**球蛋白具有2条轻链(L链),分子质量约25kDa,有κ链和λ链两种亚型,这两种轻链决定了Ig的亚型类别(IgG1IgG2IgG3IgG4)。一个天然的Ig分子两条轻链总是相同的,但在同一个体内可存在分别带有κ或λ链的抗体分子。不同种属生物体内两型轻链的比例不同,正常人血清**球蛋白κ链:λ链约为21,而在小鼠的比例为201

2.2抗体Fab段和Fc

IgG经木瓜蛋白酶酶切后裂解为2个完全相同的Fab段和1Fc,每个Fab段都为单价,可与抗原结合但不会再发生凝集反应;经胃蛋白酶酶切后裂解为1个完整F(ab)2片段和碎片化的Fc片段,F(ab)2片段为双价,可同时结合两个抗原表位。Fab段为抗原结合片段(fragment of antigen bindingFab),相当于抗体分子的两个臂,由一个完整的轻链和重链的VHCH1结构域组成。Fc段为可结晶段(fragment crystallizableFc)相当于IgCH2CH3结构域,是Ig与效应分子或者细胞相互作用的部位。Fab段包含完整的可变区,以及恒定区的CH1区域。Fc段仅指Ig恒定区CH2CH3的区域,相当于Y字结构下面那一部分。

合格 C9orf135 9号染色体开放阅读框135抗体
合格 ATF4 活化转录因子4抗体
合格 C9orf172 9号染色体开放阅读框172抗体
合格 C9orf23 9号染色体开放阅读框23抗体
合格 C9orf30 9号染色体开放阅读框30抗体
合格 C9orf37 9号染色体开放阅读框37抗体
合格 C9orf41 9号染色体开放阅读框41抗体
合格 C9orf62 9号染色体开放阅读框62抗体
合格 合格 C9orf64 9号染色体开放阅读框64抗体
合格 COX4 细胞色素c氧化酶IV亚型1抗体
合格 C9orf79 9号染色体开放阅读框79抗体
合格 MAP1LC3A 自噬微管相关蛋白轻链3抗体
合格 C9orf96 9号染色体开放阅读框96抗体
合格 C9orf98 9号染色体开放阅读框98抗体
合格 合格 合格 GPCR EX33   G蛋白偶联受体EX33蛋白抗体
合格 GPR10 G蛋白偶联受体GPR10蛋白抗体
合格 GPR105 G蛋白偶联受体GPR105蛋白抗体
合格 GPR110 protein G蛋白偶联受体GPR110蛋白抗体
合格 GPR12   G蛋白偶联受体GPR12蛋白抗体
合格 合格 Alkaline Phosphatase, Tissue Non-Specific isozyme 组织非特异性碱性磷酸酶抗体
合格 GPR30 G蛋白偶联受体GPR30蛋白抗体
合格 GPR78 G蛋白偶联受体GPR78蛋白抗体
合格 GPCR GPR86 G蛋白偶联受体GPR86蛋白抗体
合格 合格 GPR92 G蛋白偶联受体GPR92蛋白抗体
合格 合格 GPCR LGR7 G蛋白偶联受体LGR7蛋白抗体
 


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