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Anti-NDSP抗體,神經(jīng)母細(xì)胞瘤源性分泌蛋白抗體

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“Anti-NDSP抗體,神經(jīng)母細(xì)胞瘤源性分泌蛋白抗體"抗體規(guī)格0.1ml、0.2ml、1ml，抗體產(chǎn)品有效期一年，質(zhì)保三個(gè)月，質(zhì)保期內(nèi)出現(xiàn)任何質(zhì)量問(wèn)題或是出不了實(shí)驗(yàn)結(jié)果均可免費(fèi)退換。：、

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上海研盟生物科技有限公司Anti-NDSP抗體,神經(jīng)母細(xì)胞瘤源性分泌蛋白抗體*，主要應(yīng)用于WB、IHC、IF、ELISA、流式細(xì)胞術(shù)等實(shí)驗(yàn)中。說(shuō)明書隨貨發(fā)送，您也可以直接我司在線客服索取。客服

簡(jiǎn)單介紹：

中文名稱：神經(jīng)母細(xì)胞瘤源性分泌蛋白抗體

英文名稱：Anti-NDSP

產(chǎn)品編號(hào)：BYK-11711R

產(chǎn)品別名：C1orf76; NDSP; FAM163A; Chromosome 1 open reading frame 76; F163A_HUMAN; Fam163a; hypothetical protein MGC16664; NDSP; Neuroblastoma derived secretory protein; Neuroblastoma-derived secretory protein; Protein FAM163A

產(chǎn)品規(guī)格：0.1ml、0.2ml、1ml

產(chǎn)品用途：科研實(shí)驗(yàn)

產(chǎn)品價(jià)格：請(qǐng)報(bào)價(jià)

說(shuō)明書：請(qǐng)?zhí)砑涌头苯铀魅?/p>

抗體來(lái)源：該指標(biāo)有兩種產(chǎn)品，一種是兔來(lái)源抗體，一種是鼠來(lái)源抗體

克隆類型：兔來(lái)源為多克隆抗體，鼠來(lái)源單克隆抗體

交叉反應(yīng)：請(qǐng)索取說(shuō)明書查看

性狀：Lyophilized or Liquid

濃度：1mg/1ml

亞型:IgG

純化方法: affinity purified by Protein A

儲(chǔ) 存液: 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol

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-NDSP抗體,神經(jīng)母細(xì)胞瘤源性分泌蛋白抗體產(chǎn)品介紹：Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf76 gene product has been provisionally designated C1orf76 pending further characterization.

抗原修復(fù)方法：
方法1：沸水浴修復(fù)，將盛有修復(fù)液和玻片的燒杯置于沸水浴環(huán)境，保持外部沸騰狀態(tài)15min，自然冷卻至室溫。
方法2：微波修復(fù)，將盛有修復(fù)液和玻片的燒杯置于微波爐中，高火5min，停火3min，中火5min，自然冷卻至室溫。
方法3：高壓修復(fù)，修復(fù)液加入高壓鍋加熱至沸騰，放入玻片，封蓋加壓持續(xù)加熱至噴氣時(shí)開始計(jì)時(shí)修復(fù)2min，自然冷卻至室溫。
方法4：使用*修復(fù)，將*修復(fù)液加入到組織上，37℃，消化30min

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