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產(chǎn)品名稱：Anti-GATA6抗體*,GATA結合蛋白6抗體
中文名稱：GATA結合蛋白6抗體
英文名稱：Anti-GATA6
產(chǎn)品編號：BYK-1787R
產(chǎn)品別名：Gata binding factor 6; Gata binding protein 6; GATA-binding factor 6; Gata6; GATA6_HUMAN; Transcription factor Gata 6; Transcription factor GATA-6.

本公司另供應“GATA結合蛋白6抗體”的標記有：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 隆：單克隆抗體、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-GATA6抗體*,GATA結合蛋白6抗體技術說明，產(chǎn)品*，由于篇幅原因，更多信息請：

Anti-YY1/FITC  熒光素標記核轉錄因子YY1抗體IgG
Anti-ZAP-70/FITC  熒光素標記zeta相關蛋白70抗體IgG
Anti-ZCWCC1/FITC  熒光素標記ZCWCC1抗體IgG
Anti-Z-DEVD-FMK/FITC  熒光素標記CASPASE3凋亡抑制劑IgG
Anti-Zfp91/FITC  熒光素標記白血病相關新基因抗體IgG
Anti-ZNF217/FITC  熒光素標記鋅指脂蛋白217抗體IgG
Anti-ZNF268（1a）/FITC  熒光素標記鋅指脂蛋白-1a抗體IgG
Anti-ZNF268（1b）/FITC  熒光素標記鋅指脂蛋白-1b抗體IgG
Anti-ZNF268（1c）/FITC  熒光素標記鋅指脂蛋白-1c抗體IgG
Anti-ZNF300 /FITC  熒光素標記鋅指蛋白300抗體IgG
Anti-ZNF307/FITC  熒光素標記鋅指蛋白307抗體IgG
Anti-ZNF474/FITC  熒光素標記鋅指蛋白474抗體IgG
Anti-ZO-1/FITC  熒光素標記胞質(zhì)緊密粘連蛋白1抗體IgG
Anti-ZW10 peptide/FITC  熒光素標記著絲粒蛋白抗體IgG
Anti-Zyxin/FITC  熒光素標記斑聯(lián)蛋白抗體IgG
Anti-Amphetamine/FITC  熒光素標記抗毒pin苯丙胺小鼠單克隆抗體（安非他明）IgG
Anti-Amphetamine/Gold  膠體金離子標記抗毒pin苯丙胺小鼠單克隆抗體（安非他明）IgG

產(chǎn)品介紹：
This gene is a member of a small family of zinc finger transcription factors that play an important role in the regulation of cellular differentiation and organogenesis during vertebrate development. This gene is expressed during early embryogenesis and localizes to endo- and mesodermally derived cells during later embryogenesis and thereby plays an important role in gut, lung, and heart development. Mutations in this gene are associated with several congenital defects. [provided by RefSeq, Mar 2012].