植物血凝素-L(菜豆) Phytohemagglutinin-L


描述

Phytohemagglutinin-L (PHA-L), from Phaseolus Vulgaris

植物血凝素-L(菜豆)

产品标签

淋巴细胞转化实验(T Lymphocyte Transformation Test),非特异性有丝分裂原(mitogen),T细胞活化和增殖,PHA-M,PHA-P,PHA-L,PHA-E,Con A,CAS:9008-97-3

产品信息

产品名称                                                                   

产品编号          规格             价格(元)   
Phytohemagglutinin-L (PHA-L) 植物血凝素-L(菜豆) MP6301-5MG 5mg

2990

产品描述

植物血凝素(Phytohemagglutinin,PHA),多指来源于Phaseolus Vulgaris菜豆属(红腰豆)的凝集素,常用作人淋巴细胞的促有丝分裂原(mitogen),具有促进有丝分裂和诱导干扰素分泌的活性。

PHA属于高分子糖蛋白,是低聚糖(由半乳糖,N-乙酰葡糖胺和甘露糖所构成)和蛋白质形成的复合物。由4个亚基通过非共价键结合形成的四聚体糖蛋白,包含两种亚基分子,L亚基(白细胞凝集素)和E(红细胞凝集素),因此含有5种异构体(L4, L3E1, L2E2, L1E3和E4)。L亚基具有白细胞凝集和高促有丝分裂活性,E亚基具有高红细胞凝集和低促有丝分裂活性。

本品为PHA-L(Phytohemagglutinin-L),是4个L亚基通过非共价键连接形成的四聚体,经色谱纯化所得。PHA-L是白细胞凝集素,具有高促有丝分裂和白细胞凝集活性,但红细胞凝集活性极低。广泛用于免疫学研究,比如用作PBMC的刺激物;用作INF-γ ICS、ELISPOT实验的阳性对照;或用作顺行性神经示踪剂。

保存与运输方法

保存:2-8°C保存,1年有效。

运输:冰袋运输。

储存液配制

  1. 使用前室温回温至少20min,低速离心使粉末沉淀至管底。
  2. 往5mg粉末内加入1ml 10mM磷酸盐溶液,pH 8.0,轻轻漩涡震荡,使其充分溶解,若对后续实验无影响,可加入防腐剂如叠氮钠(0.04%)抑制细菌生长。

【注1】:若用于促有丝分裂实验,粉末重溶后即刻经0.22µm滤膜过滤除菌后,-20°C分装冻存,避免反复冻融,因会降低促有丝分裂活性。

【注2】:若用于顺行性神经示踪剂,5mg粉末内加入0.2ml 10mM磷酸缓冲液,pH 8.0重溶。-20°C分装冻存,避免反复冻融。

注意事项

为了您的安全和健康,请穿实验服并戴一次性手套操作。

相关产品:

货号                      产品名称                                                            规格           价格(元) 
MP6301-5MG PHA-L 植物血凝素-L(菜豆) 5mg 2990
MP6302-100UL PHA-L Solution (500×) PHA-L溶液(500×) 100μL 873
MP6303-5MG PHA-M 植物血凝素-M(菜豆) 5mg 215
MP6304-5MG PHA-E 植物血凝素-E(菜豆) 5mg 2830
MP6305-5MG PHA-P 植物血凝素-P(菜豆) 5mg 285

 

文献引用:

Quan H et al. LncRNA-AK131850 Sponges MiR-93-5p in Newborn and Mature Osteoclasts to Enhance the Secretion of Vascular Endothelial Growth Factor a Promoting Vasculogenesis of Endothelial Progenitor Cells. Cell Physiol Biochem. 2018;46(1):401-417.

After washing, cells were plated on culture dishes at the density of 5×10 6 and cultured with Microvascular Endothelial Cell Growth Medium-2 (EGM-2 MV) BulletKit (Lonza, Walkersville, MD, USA) in a humidified atmosphere of 5% CO2 at 37°C. Two days later, non-adherent cells were removed by washing with PBS twice and the culture medium was replaced every 3 d. After culturing for 1 d, 7 d, 14 d and 28 d, EPCs were identified by optical microscope observation, immunofluorescence for both Dil-Acetylated Low Density Lipoprotein (Dil-Ac- LDL; MaoKang Biotechnology, Shanghai, China) and FITC labeled Ulex Europaeus Agglutinin 1 (FITC-UEA-1; MaoKang Biotechnology, Shanghai, China), and flow cytometry (FACSCalibur Flow Cytometry, BD, Triangle, NC, USA) for PE-Cy7 conjugated anti-mouse CD34 monoclonal antibody.

 

 — — Written/Edited by V. Shallan【版权归集奇生物/MKBio金畔所有】