thrombin/Prothrombin,*Ⅱ(*II)抗原相關(guān)產(chǎn)品：
Anti-EGFRvIII(Epidermal growth factor receptor variant type Ⅲ) 表皮生長(zhǎng)因子受體III型突變體抗體
Anti-Egr-1(Early growth response 1) 早期反應(yīng)基因-1/應(yīng)急反應(yīng)生長(zhǎng)基因1抗體
Anti-phospho-eIF4E(pSer209)(phospho-Eukaryotic translation initiation factor 4E) 磷酸化eIF-4E（Ser209）抗體
Anti-ELK1 細(xì)胞轉(zhuǎn)錄因子ELK1抗體
Anti-Elastin 抗彈性蛋白抗體
Anti-ELAVL1/HuR ELAVL1抗體
Anti-Emp1 (epithelial membrane protein 1) 表皮膜蛋白1抗體
Anti-sFRP-4 抗子宮內(nèi)膜抗體
Anti-Endostatin 內(nèi)皮抑素/內(nèi)皮他丁抗體
Anti-beta endorphin (β-endorphin) 抗β內(nèi)啡肽抗體
thrombin/Prothrombin,*Ⅱ(*II)抗原產(chǎn)品詳情：
英文名稱：coagulation factor II; prothrombin; F2; Cf-2; Cf2; FII; F 2 antibody coagulation factor II (thrombin); Coagulation factor II; Coagulation factor II precursor; F2 antibody Factor II; Prothrombin; prothrombin B-chain; PT; serine protease; THRB; THRB_HUMAN; Thrombin; Thrombin heavy chain
中文名稱：*Ⅱ(*II)抗原
產(chǎn)品編號(hào)：byk-1914P
規(guī) 格：0.5mg
多肽活性：多肽
產(chǎn)品來源：合成
分 類：小分子偶聯(lián)物
偶聯(lián)蛋白：KLH
純化方法：HPLC
儲(chǔ) 存 液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
thrombin/Prothrombin,*Ⅱ(*II)抗原其他優(yōu)質(zhì)產(chǎn)品：
小鼠糖原磷酸化酶同工酶BB(GP-BB)試劑盒說明書，96T/48T代測(cè)
小鼠甲狀腺素抗體(TAb)試劑盒說明書，96T/48T代測(cè)
小鼠抗促甲狀腺素受體抗體(TRAb)試劑盒說明書，96T/48T代測(cè)
小鼠兒茶酚胺(CA)試劑盒說明書，96T/48T代測(cè)
小鼠心肌營養(yǎng)素1(CT-1)試劑盒說明書，96T/48T代測(cè)
小鼠抗α-胞襯蛋白抗體IgG/IgA(α-Fodrin IgG/IgA)試劑盒說明書，96T/48T代測(cè)
小鼠脂蛋白α(Lp-α)試劑盒說明書，96T/48T代測(cè)
小鼠*Ⅷ相關(guān)抗原(FⅧ-Ag)試劑盒說明書，96T/48T代測(cè)
小鼠*Ⅸ(FⅨ)試劑盒說明書，96T/48T代測(cè)
小鼠*Ⅹ(FⅩ)試劑盒說明書，96T/48T代測(cè)
thrombin/Prothrombin,*Ⅱ(*II)抗原保存條件：Store at -20 °C for one year. The lyophilized powder is stable at room temperature for at least one month and for greater than a year when kept at -20°C. Upon reconstituted, aliquot and store at -20°C or -80°C. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹：Coagulation factor II is proteolytically cleaved to form thrombin in the first step of the coagulation cascade which ultimay results in the stemming of blood loss. F2 also plays a role in maintaining vascular integrity during development and postnatal life. Mutations in F2 leads to various forms of thrombosis and dysprothrombinemia.
Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing. Involvement in disease:
Defects in F2 are the cause of factor II deficiency (FA2D) . It is a very rare blood coagulation disorder characterized by mucocutaneous bleeding symptoms. The severity of the bleeding manifestations correlates with blood factor II levels
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