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Anti-Human uPA/Urokinase Rabbit Recombinant Antibody, PBS Only

uPA/Urokinase Uni-rAb® Recombinant Antibody for FC
Cat No. 98824-2-PBS

产品说明书

CloneNo. 252624A9

宿主/亚型

Rabbit / IgG

种属反应性

human

应用

FC

PLAU, UPA, ATF, EC:3.4.21.73, u PA

缓冲液配方:  PBS Only
PBS, Azide
PBS Only
偶联物:  Unconjugated
规格价格库存


产品信息

98824-2-PBS targets uPA/Urokinase in FC applications and shows reactivity with human samples.

经测试应用 FC Application Description
经测试反应性 human
免疫原

CatNo: Eg7083

Product name: Recombinant human PLAU/uPA protein

Source: mammalian cells-derived, pHZ-KIsec-C-rFc

Tag: C-rFc

Domain: 21-431 aa of NM_002658.6

Sequence: SNELHQVPSNCDCLNGGTCVSNKYFSNIHWCNCPKKFGGQHCEIDKSKTCYEGNGHFYRGKASTDTMGRPCLPWNSATVLQQTYHAHRSDALQLGLGKHNYCRNPDNRRRPWCYVQVGLKLLVQECMVHDCADGKKPSSPPEELKFQCGQKTLRPRFKIIGGEFTTIENQPWFAAIYRRHRGGSVTYVCGGSLISPCWVISATHCFIDYPKKEDYIVYLGRSRLNSNTQGEMKFEVENLILHKDYSADTLAHHNDIALLKIRSKEGRCAQPSRTIQTICLPSMYNDPQFGTSCEITGFGKENSTDYLYPEQLKMTVVKLISHRECQQPHYYGSEVTTKMLCAADPQWKTDSCQGDSGGPLVCSLQGRMTLTGIVSWGRGCALKDKPGVYTRVSHFLPWIRSHTKEENGLAL

种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Recombinant
产品类型 Antibody
全称 plasminogen activator, urokinase
别名 PLAU, UPA, ATF, EC:3.4.21.73, u PA
计算分子量49kDa
GenBank蛋白编号NM_002658.6
基因名称 Urokinase
Gene ID (NCBI) 5328
RRIDAB_3746365
偶联类型 Unconjugated
形式Liquid
纯化方式Protein A purification
UNIPROT IDP00749-1
储存缓冲液 PBS only, pH 7.3.
储存条件Store at -80°C.
The product is shipped with ice packs. Upon receipt, store it immediately at -80°C

背景介绍

uPA (Urokinase-type plasminogen activator) is also named as Urokinase or PLAU, and belongs to the peptidase S1 family. uPA initiates a proteolytic cascade, which degrades the extracellular matrix during tissue growth and remodelling. The secreted proform of uPA is activated after binding to a specific high-affinity cell surface receptor. Secreted UPA is exposed to rapid inactivation in the pericellular space by plasminogen activator inhibitor-1 (PAI-1), which is stored in the extracellular matrix bound to vitronectin (PMID: 9665342). It has 2 isoforms produced by alternative splicing. Defects in uPA are the cause of Quebec platelet disorder (QPD).

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