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當(dāng)前位置:上海博研生物工程研究中心>>科研抗體>>一抗>> Anti-Histone H3-like protein抗體,組蛋白H3樣抗體巨額讓利

Anti-Histone H3-like protein抗體,組蛋白H3樣抗體巨額讓利

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上海博研生物工程研究中心為您現(xiàn)貨提供*的產(chǎn)品與服務(wù),本中心產(chǎn)品齊全,保證實驗的有效性,提供,是您科研實驗產(chǎn)品的一站式平臺,咨詢。!

產(chǎn)品名稱:Anti-Histone H3-like protein抗體,組蛋白H3樣抗體巨額讓利
中文名稱:組蛋白H3樣抗體
英文名稱:Anti-Histone H3-like protein
產(chǎn)品編號:BYK-0483R
產(chǎn)品別名:centromere-specific H3 variant protein.

本公司另供應(yīng)“組蛋白H3樣抗體”的標(biāo)記有:Alexa Fluor 350 Alexa Fluor 488 Alexa Fluor 555 Alexa Fluor 647 AP APC Biotin Cy3 Cy5 Cy5.5 Cy7 FITC Gold HRP PE PE-Cy3 PE-CY5 PE-CY5.5 PE-CY7 RBITC.
產(chǎn)品規(guī)格:100ug/200ug
產(chǎn)品濃度: 1mg/1ml
抗體來源:兔源、鼠源、山羊
克 ?。簡慰寺】贵w、多克隆抗體
抗體類型:一抗
性 狀: 凍干粉或液體
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.

Anti-Histone H3-like protein抗體,組蛋白H3樣抗體巨額讓利技術(shù)說明,產(chǎn)品*,由于篇幅原因,更多信息請:

Anti-CXCR3/CD183  細胞表面趨化因子受體3抗體/G蛋白偶聯(lián)受體
Anti-Gastrin(Bombesin)  胃泌素/蛙皮素抗體
Anti-Gastrin(Bombesin)  胃泌素/蛙皮素抗體
Anti-Gastrin receptor(Gastrin /cholecystokinin type B receptor)  促胃泌素受體抗體
Anti-GATA-3(GATA binding factor 3)  抗GATA結(jié)合蛋白3抗體
Anti-GATA-4(GATA binding factor 4)  抗GATA結(jié)合蛋白4抗體
Anti-GATA-5(GATA binding factor 5)  抗GATA結(jié)合蛋白5抗體
Anti-GATA-6(GATA binding factor 6)  抗GATA結(jié)合蛋白6抗體
Anti-Gax(growth arrest-specific homeobox)  生長終止特異性同源盒基因抗體
Anti-GCP-2/CXCL6(granulocyte chemotactic protein 2)  抗粒細胞趨化蛋白2抗體
Anti-CXCL7/NAP-2/PPBP(C-X-C motif chemokine 7)  中性粒細胞趨化蛋白2抗體
Anti-CXCL9/MIG/CMK  γ干擾素誘導(dǎo)單核細胞因子抗體
Anti-CXCL11/ITAC/SCYB11  干擾素誘導(dǎo)T細胞趨化因子抗體
Anti-CXCL13/BLC-1(C-X-C motif chemokine 13)  B-淋巴細胞趨化因子抗體
Anti-CXCL15/Lungkine  趨化因子CXCL15體
Anti-GCK/GLK(Glucokinase)  抗葡萄糖激酶抗體
Anti-GAPDH(兔來源免疫組化用抗體)rat、mouse  3-磷酸甘油醛脫氫酶(大鼠、小鼠)(兔來源免疫組化用抗體)
Anti-GAPDH(兔來源免疫組化用抗體)  3-磷酸甘油醛脫氫酶(兔來源免疫組化用抗體)
Anti-Gαi-3(G alpha i-3)  抑制型G蛋白α3抗體

產(chǎn)品介紹:

Histones are highly conserved proteins that serve as the structural scaffold for the organization of nuclear DNA into chromatin. The four core histones, H2A, H2B, H3, and H4, assemble into an octamer (2 molecules of each). Subsequently, 146 base pairs of DNA are wrapped around the octamer, forming a nucleosome, the basic subunit of chromatin. Histone modifications regulate DNA transcription, repair, recombination, and replication. The most commonly studied modifications are acetylation, phosphorylation, methylation, and ubiquitination. These modifications can alter local chromatin architecture, or recruit trans-acting factors that recognize specific histone modifications (the "histone code" hypothesis). Trimethylation of histone H3 on Lys9 (H3K9me3) is one of the most highly studied epigenetic marks. H3K9me3 functions in the repression of euchromatic genes, and in epigenetic control of heterochromatin assembly, most likely via acting as a recognition motif for the binding of chromatin-associated proteins, such as Swi6 or HP1Alpha/Beta. The enzymes responsible for H3K9me3 formation are SUV39H1 and SUV39H2.

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