重组人CPVL(卵黄羧肽酶样蛋白)

特别提示：包括重组人CPVL(卵黄羧肽酶样蛋白)在内，本公司的所有产品仅可用于科研实验，严禁用于临床医疗及其他非科研用途！

产品名称：重组人CPVL(卵黄羧肽酶样蛋白)
英文名称：Recombinant Human Vitellogenic carboxypeptidase-like protein
产品货号：JN1768
产品规格：10μg|50μg|500μg|1mg

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Leu23-Gly476在C端含有His标签。

CPVL质量控制：＞95%(还原性SDS-PAGE)

CPVL制剂：液体

CPVL保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。

关于CPVL：
Probable serine carboxypeptidase CPVL, also known as Carboxypeptidase, vitellogenic-like, Vitellogenic carboxypeptidase-like protein, is a member of the peptidase S10 family. It is expressed in macrophages but not in other leukocytes. And specifically, it is abundantly expressed in heart and kidney, also expressed in spleen, leukocytes, and placenta. This enzyme may be involved in the digestion of phagocytosed particles in the lysosome, and also participation in an inflammatory protease cascade, and trimming of peptides for antigen presentation.

除了重组人CPVL(卵黄羧肽酶样蛋白),，我公司还供应以下相关产品：



名称：重组小鼠成纤维生长因子9
货号：JN0283
规格：10μg|50μg|500μg|1mg
本品由我们的大肠杆菌表达系统制备，目的基因编码的Met1­Ser208在C端含有His标签。

FGF-9质量控制：＞95%(还原性SDS-PAGE)。

FGF-9制剂：液体

FGF-9保存：
收到后请置于-20℃，可稳定保存6个月，避免反复冻融。

关于FGF-9：
Fibroblast growth factor-9 (FGF-9) is an approximately 26 kDa secreted glycoprotein of the FGF family. Secreted mouse FGF-9 lacks the N-terminal 1-3 aa and shares >98% sequence identity with rat, human, equine, porcine and bovine FGF-9. FGF-9 plays an important role in the regulation of embryonic development, cell proliferation, cell differentiation and cell migration. In the mouse embryo the location and timing of FGF-9 expression affects development of the skeleton, cerebellum, lungs, heart, vasculature, digestive tract, and testes .It may have a role in glial cell growth and differentiation during development, gliosis during repair and regeneration of brain tissue after damage, differentiation and survival of neuronal cells, and growth stimulation of glial tumors. Deletion of mouse FGF-9 is lethal at birth due to lung hypoplasia, and causes rhizomelia, or shortening of the proximal skeleton. An unusual constitutive dimerization of FGF 9 buries receptor interaction sites which lowers its activity, and increases heparin affinity which inhibits diffusion. A spontaneous mouse mutant, Eks, interferes with dimerization, resulting monomeric, diffusible FGF-9 that causes elbow and knee synostoses (joint fusions) due to FGF-9 misexpression in developing joints.