Anti-beta glucuronidase抗体,β葡萄糖醛酸苷酶抗体科研产品介绍：
Defects in GUSB are the cause of mucopolysaccharidosis type 7 (MPS7) ; also known as Sly syndrome. MPS7 is an autosomal recessive lysosomal storage disease characterized by inability to degrade glucuronic acid-containing glycosaminoglycans. The phenotype is highly variable, ranging from severe lethal hydrops fetalis to mild forms with survival into adulthood. Most patients with the intermediate phenotype show hepatomegaly, skeletal anomalies, coarse facies, and variable degrees of mental impairment. Mucopolysaccharidosis type 7 is associated with non-immune hydrops fetalis, a generalized edema of the fetus with fluid accumulation in the body cavities due to non-immune causes. Non-immune hydrops fetalis is not a diagnosis in itself but a symptom, a feature of many genetic disorders, and the end-stage of a wide variety of disorders.
与“Anti-beta glucuronidase抗体,β葡萄糖醛酸苷酶抗体科研”有关的产品：
Anti-CK7 (Cytokeratin 7)ret mouse 抗细胞角蛋白7抗体(大、小鼠)
Anti-CK5+6 (Cytokeratin 5+6) 细胞角蛋白5+6抗体
Anti-CK6 (Cytokeratin 6) 细胞角蛋白6抗体
Anti-CK8(Cytokeratin 8) 细胞角蛋白8抗体
Anti-CKLFSF2（human）（chemokine-like factor superfamily 2） 人类新细胞因子/趋化素样因子超家族成员2抗体
Anti-CK1+5+10+14 高分子量角蛋白抗体
Anti-CK-HMW 高分子量细胞角蛋白抗体
anti-CKIP-1（casein kinase 2 interaction protein 1） 酪蛋白激酶2相互作用蛋白1抗体
Anti-Clostridium perfringens type D 兔抗D型产气荚膜梭菌抗体
Anti-CLCA4(Calcium-activated chloride channel 4) 钙激活氯离子通道4抗体
产品详情：
产品编号：HRK-7980R
产品规格: 0.1ml/0.2ml
产品别名：asd; Beta G1; Beta glucuronidase; Beta-G1; Beta-glucuronidase; BG; BGLR; BGLR_HUMAN; Glucuronidase beta; Gur; Gus; Gus-r; Gus-s; Gus-t; Gus-u; GUSB; Gut; MPS7; Ac2-223
产品价格：询价(电询或客服)
产品用途：科研实验
贮 存： 贮存于-20℃.
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