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產(chǎn)品名稱：跨膜蛋白106B（Anti-TMEM106B）抗體*
中文名稱：跨膜蛋白106B抗體
英文名稱：Anti-TMEM106B
產(chǎn)品編號(hào)：BYK-11694R
產(chǎn)品別名：Tmem106b; Transmembrane protein 106B; 2310036D22Rik; 5830455K21Rik; 6430519M21Rik; AI428776; AI661344; FLJ11273; LRRGT00101; MGC33727; MGC94135; T106B_HUMAN.

本公司另供應(yīng)“跨膜蛋白106B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、其他
克 ?。?jiǎn)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.

跨膜蛋白106B（Anti-TMEM106B）抗體*技術(shù)說明，產(chǎn)品*，由于篇幅原因，更多信息請(qǐng)：

Anti-VTN（Vitronectin）  玻璃粘連蛋白抗體
Anti-VTG（vilogenin）  卵黃蛋白原抗體
Anti-VWF（Von Willebrand Factor）  血管假性血友病因子/血管性血友病因子抗體
Anti-V.cholera Ogawa（Vibrio cholerae O1 Serotype Ogawa）  01群稻葉型霍亂弧菌抗體
Anti-V.cholera Ogawa（Vibrio cholerae O1 serotype Ogawa）  01群小川型霍亂弧菌抗體
Anti-WEE1 protein  WEE1蛋白抗體
Anti-WNK4（Ser/Thr-protein kinase WNK4; protein kinase with no lysine 4; protein kinase, lysine –dficient 4）  一種新的*/*激酶家族成員的基因WNK4抗體
Anti-WNK3 protein（Serine/threonine-protein kinase WNK3）  */*激酶家族成員的基因WNK3抗體
Anti-Wnt1  信號(hào)通路Wnt1抗體
Anti-WDR26/MIP2   心肌缺血預(yù)處理正調(diào)節(jié)蛋白2抗體
Anti-Visfatin-1/PBEF1（NT）  內(nèi)脂素/內(nèi)臟脂肪素/腹脂素/內(nèi)肥素（小鼠抗人、大、小鼠、猴：N端多肽）
Anti-Visfatin-1/PBEF1（NT） hu、 mo、 rat、MK  內(nèi)脂素/內(nèi)臟脂肪素（N端抗體）
Anti-Visfatin-1/PBEF1（NT） Human  內(nèi)脂素/內(nèi)臟脂肪素（N端抗體）
Anti-Visfatin-2（CT）  內(nèi)脂素/內(nèi)臟脂肪素（C端抗體）
Anti-VR1（Vanilloid receptor subtype1）  辣椒素受體抗體
Anti-VSIG4（V-set and immunoglobulin domain-containing protein 4）  T淋巴細(xì)胞負(fù)調(diào)節(jié)蛋白之一抗體

產(chǎn)品介紹：

TMEM106B is a 274 amino acid single-pass membrane protein that is encoded by a gene which maps to human chromosome 7. Chromosome 7 houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders, including cases of acute myelogenous leukemia and myelodysplasia.