重组人激肽释放酶(Kallikrein 11)(KLK11)

特别声明：本产品及我公司所售其他产品均为科研类试剂产品，严禁用于药物、医疗及其他非科研用途。

重组人激肽释放酶(Kallikrein 11)(KLK11)优惠价的品牌：百奥莱博，是优质的分子生物学试剂产品，用于科研实验，本产品质量好，且极具价格优势，深为用户称道，了解更多重组人激肽释放酶(Kallikrein 11)(KLK11)等分子生物学试剂产品请联系我司咨询订购。

名称：重组人激肽释放酶(Kallikrein 11)(KLK11)优惠价
编号：JN1710
品牌：百奥莱博
规格：10μg|50μg|500μg|1mg
产地：国产|进口
本品由我们的哺乳动物细胞表达系统制备而成，目的基因编码的Glu19-Asn250在C端含有His标签。

Kallikrein 11质量控制：＞95%(还原性SDS-PAGE)

Kallikrein 11制剂：液体

Kallikrein 11保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。

关于Kallikrein 11：
Human Kallikrein 11 (KLK11) is a member of tissue kallikrein family which are extracellular serine proteases consisting of 15 members. Two isoforms of KLK11 are differentially expressed. Isoform 1 is predominantly expressed in brain and isoform 2 is preferentially expressed in prostate. Isoform 1 consists of a signal peptide,a short pro peptide and the mature chain.Isoform 2 contains an extra 32 amino acid N terminal to full-length isoform 1.KLK11 is a novel marker for ovarian and prostate cancer carcinomas. KLK11 can be activated by thermolysin and is active against a thioester substrate.

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重组人激肽释放酶(Kallikrein 11)(KLK11)优惠价关键词：重组人Kallikrein 11,重组人激肽释放酶,重组人激肽释放酶蛋白,重组人KLK11,JN1710

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重组人激肽释放酶(Kallikrein 11)(KLK11)优惠价关键词：重组人Kallikrein 11,重组人激肽释放酶,重组人激肽释放酶蛋白,重组人KLK11,JN1710


·重组人磷酸丙糖异构酶(TIM)
编号：JN2030
英文名称：Recombinant Human Triosephosphate Isomerase
规格：10μg|50μg|500μg|1mg
本品由我们的大肠杆菌表达系统制备而成，目的基因编码的Met1-Gln249在N端含有His标签。

TIM质量控制：＞95%(还原性SDS-PAGE)

TIM制剂：液体

TIM保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。

关于TIM：
Triose-phosphate isomerase, also named Triose-phosphate isomerase, TPI and TIM, is an enzyme that catalyzes the reversible interconversion of the triose phosphate isomers dihydroxyacetone phosphate and D-glyceraldehyde 3-phosphate. TPI has been found in nearly every organism searched for the enzyme, including animals such as mammals and insects as well as in fungi, plants, and bacteria. However, some bacteria that do not perform glycolysis, like ureaplasmas, lack TPI. TPI plays an important role in glycolysis and is essential for efficient energy production. TPI deficiency is an autosomal recessive disorder and the most severe clinical disorder of glycolysis. Triose phosphate isomerase deficiency is associated with neonatal jaundice, chronic hemolytic anemia, progressive neuromuscular dysfunction, cardiomyopathy and increased susceptibility to infection and characterized by chronic hemolytic anemia.

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