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產品名稱：Anti-PROSAAS抗體-枯草溶菌素轉化酶1抑制劑抗體【客戶好評】
中文名稱：枯草溶菌素轉化酶1抑制劑抗體
英文名稱：Anti-PROSAAS
產品編號：BYK-11686R
產品別名：b-LEN; b-PEN-LEN; b-SAAS; Big LEN; granin like neuroendocrine peptide; l-LEN; l-SAAS; N-proSAAS; PCSK1_HUMAN; Pcsk1n; pro-SAAS; Proprotein convertase 1 inhibitor; Proprotein convertase subtilisin/kexin type 1 inhibitor; PROSAAS; SAAS; SAAS CT（1-49）; SAAS CT（25-40）.
本公司另供應“枯草溶菌素轉化酶1抑制劑抗體”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.
產品規(guī)格：100ug/200ug
產品濃度： 1mg/1ml
抗體來源：兔源、鼠源、其他
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-PROSAAS抗體-枯草溶菌素轉化酶1抑制劑抗體【客戶好評】技術說明，產品*，由于篇幅原因，更多信息請：
Anti-CXCL16（CXC-chemokine ligand 16） CXC趨化因子16抗體
Anti-Secretin 分泌素抗體
Anti-Secretin receptor 分泌素受體抗體
Anti-SEL1L（Suppressor of lin-12-like Protein） SEL1L抗體
Anti-Selenoprotein W 硒蛋白W抗體
Anti-Sema3A （semaphorin 3A） 臂板蛋白3A抗體
Anti-Sema3F （semaphorin 3F） 臂板蛋白3F抗體
Anti-Sema4C （semaphorin 4C） 臂板蛋白4C抗體
Anti-SFRP1（Secreted frizzled related protein 1） 分泌型卷曲相關蛋白1抗體
Anti-SGC （soluble glycoprotein C） 可溶性糖蛋白C抗體
Anti-SGLT1 （sodium-glucose cotransporter1） 鈉-葡萄糖共轉運載體1抗體
Anti-Shank1（SH3 and multiple anleyrin repead domins protein 1） shank-1抗體
Anti-Shadow/SPRN（Shadow of prion protein precursor） 新朊蛋白/朊蛋白相關蛋白/沙杜（Shadoo）蛋白抗體
Anti-SDF-1/CXCL12 （stromal cell derived factor-1） 基質細胞衍生因子－1抗體
Anti-CXCL14/BRAK（C-X-C motif chemokine 14） CXC趨化因子14抗體
產品介紹：
PCSK1N is a 260 amino acid protein that is both secreted and localized to the trans-Golgi network. Expressed in pancreas and brain, PCSK1N is thought to play a role in the control of the neuroendocrine secretory pathway and may also be involved in PCSK1 inhibition. The gene encoding PCSK1N maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination, as an X and a Y chromosome lead to normal male development, while two copies of an X chromosome lead to normal female development. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
