JN1670型重组人XPNPEP1现货促销

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。

JN1670型重组人XPNPEP1现货促销是高品质的分子生物学试剂产品，由北京百奥莱博供应，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XPNPEP1等分子生物学试剂产品请联系我司咨询订购。

名称：JN1670型重组人XPNPEP1现货促销
产地：国产|进口
英文名：Recombinant Human Xaa-Pro Aminopeptidase 1
品牌：百奥莱博
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Pro2-His623在C端含有His标签。

XPNPEP1质量控制：＞95%(还原性SDS-PAGE)

XPNPEP1制剂：液体

XPNPEP1保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。

关于XPNPEP1：
X-Prolyl Aminopeptidase (XPNPEP1) is a proline-specific metalloaminopeptidase that specifically catalyzes the removal of any unsubstituted N-terminal amino acid that is adjacent to a penultimate proline residue. Because of its specificity toward proline, it has been suggested that X-Prolyl Aminopeptidase is important in the maturation and degradation of peptide hormones, neuropeptides, and tachykinins, as well as in the digestion of otherwise resistant dietary protein fragments, thereby complementing the pancreatic peptidases. X-Prolyl Aminopeptidase is a member of the M24 family of metalloproteases, which also contains methionine aminopeptidases, X-Pro dipeptidase, aminopeptidase P2, aminopeptidase P homolog, proliferation-associated protein 1, and suppressor of Ty homolog or chromatin-specific transcription elongation factor large subunit. It is a soluble enzyme, in contrast to the GPI-anchored Aminopeptidase P2 encoded by XPNPEP2. Deficiency of X-Prolyl Aminopeptidase results in excretion of large amounts of imino-oligopeptides in urine. Human Aminopeptidase P1 is widely expressed. The amino acid sequence of human X-Prolyl Aminopeptidase is 99%, 97%, 95%, 74% and 73% identical to that of canine, bovine, mouse/rat, Xenopus and zebrafish, respectively.

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·重组小鼠外异蛋白A受体(Edar)
编号：JN1435
英文名称：Recombinant Mouse Ectodysplasin Receptor
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Glu27-Ile189在C端带有Fc标签。

EDAR 质量控制：＞95%(还原性SDS-PAGE)

EDAR 制剂：冻干品

EDAR 保存：
冻干蛋白置于-20℃以下可长期保存，室温条件下可稳定保存3周。
复溶蛋白溶液可在4～7℃保存2～7天，可分装后置于-20℃保存三个月。

EDAR 复溶：
打开试剂管前请先离心。
复溶浓度推荐大于100 μg/ml。
冻干蛋白请溶于ddH2O。
复溶后，请根据用量分装冻存，避免反复冻融。

关于EDAR ：
Ectodysplasin A receptor (EDAR) is a type I transmembrane protein of the TNF-α receptor superfamily which plays a key role in ectodermal differentiation. EDAR was encoded by the mouse downless gene and defective in human dominant and recessive forms of autosomal hypohidrotic ectodermal dysplasia (EDA) syndrome. The extracellular domain of EDAR contains 14 cysteine residues, six of which approximate the TNFRSF cysteine-rich region, the cytoplasmic domain contains a region with homology to the death domains found in other TNFRSF members. EDAR has been suggested to be an early and important promoter of placode development in all ectodermal organs, such as uch as hair follicles, teeth and sweat glands. EDA-A1, the A1 isoform of EDA, is the EDAR ligand. EDA and EDA are implicated in appendage development by the cloning of a gene underlying hypohidrotic ectodermal dysplasia (HED) in mouse and human. HED is characterized by agenesis or malformation of ectoderm-derived appendages, such as teeth, sweat glands and hair follicles, while the skin itself develops normally.


JN1670型重组人XPNPEP1现货促销关键词：重组人XPNPEP1蛋白,重组XPNPEP1,Recombinant Human Xaa-Pro Aminopeptidase 1,百奥莱博,JN1670


·重组人酪*酸蛋白激酶BLK
编号：JN1774
英文名称：Recombinant Human Tyrosine-Protein Kinase BLK
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Gly2-Pro505在C端含有His标签。

BLK质量控制：＞95%(还原性SDS-PAGE)

BLK制剂：液体

BLK保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。

关于BLK：
Tyrosine-Protein Kinase Blk (BLK) contains one protein kinase domain, one SH2 domain and one SH3 domain. BLK is a non-receptor tyrosine kinase, which is involved in B-lymphocyte development, differentiation and signaling. B-cell receptor (BCR) signaling requires a tight regulation of several protein tyrosine kinases and phosphatases, and associated coreceptors. Signaling through BLK plays an important role in transmitting signals through surface immunoglobulines and supports the pro-B to pre-B transition, as well as the signaling for growth arrest and apoptosis downstream of B-cell receptor. Defects in BLK are a cause of maturity-onset diabetes of the young type 11 (MODY11).


JN1670型重组人XPNPEP1现货促销关键词：重组人XPNPEP1蛋白,重组XPNPEP1,Recombinant Human Xaa-Pro Aminopeptidase 1,百奥莱博,JN1670


·重组人磷酸甲羟戊酸激酶(PMVK)
编号：JN2018
英文名称：Recombinant Human Phosphomevalonate Kinase
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-Leu192在N端含有His标签。

PMVK质量控制：＞95%(还原性SDS-PAGE)

PMVK制剂：液体

PMVK保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。

关于PMVK：
Phosphomevalonate kinase (PMVK) is a cytosolic enzyme. PMVK can be highly expressed in the heart,skeletal muscle, liver, pancreas, and kidney; it is expressed at lower levels in the brain, lung, and placenta. Induced by sterol, PMVK takes part in isopentenyl diphosphate biosynthesis through the mevalonate pathway. PMVK catalyzes the conversion of mevalonate 5-phosphate into mevalonate 5-diphosphate in the fifth reaction of the cholesterol biosynthetic pathway.

我公司正在火爆促销分子生物学试剂系列产品，欢迎您的垂询选购JN1670型重组人XPNPEP1现货促销。