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華瑞科研網(wǎng)-ELISA試劑盒
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更新時(shí)間:2018-04-07 10:16:49瀏覽次數(shù):405次
聯(lián)系我時(shí),請告知來自 智慧城市網(wǎng)“Anti-BSCL2抗體,先天性脂肪代謝障礙蛋白2抗體科研"我公司擁有*的細(xì)胞服務(wù)技術(shù),*的儀器設(shè)備和專業(yè)的ELISA檢測試劑盒、生物索標(biāo)記、熒光索標(biāo)記、酶標(biāo)記等,廣泛用于多種分析研究與技術(shù)測定。咨詢,我們將竭誠為你服務(wù)!
Anti-BSCL2抗體,先天性脂肪代謝障礙蛋白2抗體科研產(chǎn)品介紹:
Defects in BSCL2 are the cause of congenital generalized lipodystrophy type 2 (CGL2) . Congenital generalized lipodystrophy is an autosomal recessive disorder characterized by a near absence of adipose tissue, extreme insulin resistance, hypertriglyceridemia, hepatic steatosis and early onset of diabetes.
Defects in BSCL2 are the cause of spastic paraplegia type 17 (SPG17) ; also known as Silver spastic paraplegia syndrome. Spastic paraplegia is a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. SPG17 is characterized by prominent amyotrophy of the hand muscles, the presence of mild to severe pyramidal tract signs, and spastic paraplegia.
SPG17 is a motor neuron disease overlapping with distal spinal muscular atrophy type 5. Defects in BSCL2 are a cause of distal hereditary motor neuropathy type 5 (HMN5); also known aS distal hereditary motor neuropathy type V (DSMAV). HMN5 is an autosomal dominant disorder characterized by degeneration of motor nerve fibers, predominantly in limb distal regions.
與“Anti-BSCL2抗體,先天性脂肪代謝障礙蛋白2抗體科研"有關(guān)的產(chǎn)品:
Anti-CKⅠα/STK(Casein kinase Ⅰα/Serine/Threonine Protein KinaseⅠα/) 屬絲/*蛋白質(zhì)激酶抗體
Anti-CKⅡα/STK(Casein kinase Ⅱα;Serine/Threonine Protein KinaseⅡα) 屬絲/*蛋白質(zhì)激酶抗體
Anti-CKⅡα/STK(Casein kinase Ⅱα;Serine/Threonine Protein KinaseⅡα) 屬絲/*蛋白質(zhì)激酶抗體
Anti-P-CK(pan-cytokeratin) 廣譜細(xì)胞角蛋白抗體
Anti-CK18(Cytokeratin 18) 細(xì)胞角蛋白18抗體
Anti-CK18(Cytokeratin 18)C-term 細(xì)胞角蛋白18抗體(C端)
Anti-CK18(Cytokeratin 18) 細(xì)胞角蛋白18抗體
Anti-CK14/17/42/10 細(xì)胞角蛋白14抗體
Anti-CK15(Cytokeratin 15) 細(xì)胞角蛋白15抗體
Anti-CK16(Cytokeratin 16) 細(xì)胞角蛋白16抗體
產(chǎn)品詳情:
產(chǎn)品編號:HRK-6311R
產(chǎn)品規(guī)格: 0.1ml/0.2ml
產(chǎn)品別名:Bernardinelli Seip congenital lipodystrophy 2; Bernardinelli Seip congenital lipodystrophy type 2 protein; Bernardinelli-Seip congenital lipodystrophy type 2 protein; BSCL 2; BSCL2; BSCL2_HUMAN; GNG3LG; HMN 5; HMN5; MGC4694; Seipin; Spastic paraplegia 17 (autosomal dominant); Spastic paraplegia 17 (Silver syndrome); Spastic paraplegia 17; Spastic paraplegia with amyotrophy of hands and feet (Silver syndrome); Spastic paraplegia with amyotrophy of hands and feet; SPG 17; SPG17
產(chǎn)品價(jià)格:詢價(jià)(電詢或客服)
產(chǎn)品用途:科研實(shí)驗(yàn)
貯 存: 貯存于-20℃.
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