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β葡萄糖醛酸苷酶重組兔單抗

簡(jiǎn)要描述：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 impai

  • 產(chǎn)品型號(hào)：bsm-62371R
  • 廠商性質(zhì)：生產(chǎn)廠家
  • 更新時(shí)間：2025-03-03
  • 訪  問(wèn)  量： 161

詳細(xì)介紹

Human
WB,IHC-P,IHC-F,ICC/IF,IF,Flow-Cyt
Store at 4℃ for short term. Store at -20℃ for long term. Avoid repeated freeze/thaw cycles.

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    請(qǐng)輸入計(jì)算結(jié)果（填寫阿拉伯?dāng)?shù)字），如：三加四=7