巨噬细胞炎性蛋白3α(MIP3a)活性蛋白

Active Macrophage Inflammatory Protein 3 Alpha (MIP3a)

CCL20; CKb4; LARC; MIP3-A; SCYA20; ST38; Small Inducible Cytokine Subfamily A(Cys-Cys)Member 20; Beta-Chemokine Exodus-1; Liver And Activation-Regulated Chemokine

  • 巨噬细胞炎性蛋白3α(MIP3a)活性蛋白 产品包装(模拟)
  • 巨噬细胞炎性蛋白3α(MIP3a)活性蛋白 产品包装(模拟)
  • 巨噬细胞炎性蛋白3α(MIP3a)活性蛋白 Figure. Gene Sequencing (Extract)
  • APA095Hu01.png Figure. SDS-PAGE
  • Certificate 通过ISO 9001、ISO 13485质量体系认证

活性实验

Macrophage Inflammatory Protein 3 Alpha (MIP-3α), also known as LARC (liver and activation-regulated chemokine), Exodus-1 or CCL20, is a CC chemokine with a selective chemotactic activity for lymphocytes and dendritic cells (DCs). MIP3α is produced by activated cells, including monocytes, T cells, endothelial cells, epithelial cells, and fibroblasts and is expressed in liver, lung, and some lymphoid tissues. This chemokine elicits its effects on its target cells by binding to the chemokine receptor CCR7. It attracts certain cells of the immune system, including dendritic cells and antigen-engaged B cells, CCR7 central-memory T-Cells. Thus, chemotaxis assay used 24-well microchemotaxis system was undertaken to detect the chemotactic effect of recombinant human MIP-3α on the Jurkat cell line. Briefly, Jurkat cells were seeded into the upper chambers (200μL cell suspension,106 cells/mL in RPMI 1640 with FBS free) and MIP-3α (0.01ng/mL, 0.1ng/mL, 1ng/mL, 10ng/mL,100ng/mL and 1000ng/mL diluted separately in serum free RPMI 1640 ) was added in lower chamber with a polycarbonate filter (8 μm pore size) used to separate the two compartments. After incubation at 37℃ with 5% CO2 for 2h, the filter was removed, then cells in low chamber were observed by inverted microscope at low magnification (×100) and the number of migrated cells were counted at high magnification (×400) randomly (five fields for each filter). Result shows MIP-3α is able to induce migration of Jurkat cells. The migrated Jurkat cells in low chamber at low magnification (×100) were shown in Figure 1. Five fields of each chamber were randomly chosen, and the migrated cells were counted at high magnification (×400). Statistical results were shown in Figure 2. The optimum chemotaxis of recombinant human MIP-3α occurs at 1-10ng/mL.

Figure 2. The chemotactic effect of recombinant human MIP-3α on Jurkat cells

用法

Reconstitute in 10mM PBS (pH7.4) to a concentration of 0.1-1.0 mg/mL. Do not vortex.

储存

避免反复冻融。2-8°C不超过一个月,-80°C不超过12个月。

稳定性

热稳定性以损失率显示。损失率是由加速降解试验决定,具体方法如下:在37°C孵育48小时,没有显著的降解或者沉淀产生。保质期内,在适当的条件下存储,损失率低于5%。

相关产品

编号 适用物种:Homo sapiens (Human,人) 应用(仅供研究使用,不用于临床诊断!)
RPA095Hu01 巨噬细胞炎性蛋白3α(MIP3a)重组蛋白 Positive Control; Immunogen; SDS-PAGE; WB.
APA095Hu01 巨噬细胞炎性蛋白3α(MIP3a)活性蛋白 Cell culture; Activity Assays.
RPA095Hu02 巨噬细胞炎性蛋白3α(MIP3a)重组蛋白 Positive Control; Immunogen; SDS-PAGE; WB.
APA095Hu02 巨噬细胞炎性蛋白3α(MIP3a)活性蛋白 Cell culture; Activity Assays.
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MAA095Hu22 巨噬细胞炎性蛋白3α(MIP3a)单克隆抗体 WB; IHC; ICC; IP.
MAA095Hu23 巨噬细胞炎性蛋白3α(MIP3a)单克隆抗体 WB; IHC; ICC; IP.
MAA095Hu24 巨噬细胞炎性蛋白3α(MIP3a)单克隆抗体 WB; IHC; ICC; IP.
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MAA095Hu27 巨噬细胞炎性蛋白3α(MIP3a)单克隆抗体 WB; IHC; ICC; IP.
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LMA095Hu 巨噬细胞炎性蛋白3α(MIP3a)等多因子检测试剂盒(流式荧光发光法) FLIA Kit for Antigen Detection.
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参考文献

杂志 参考文献
Medicine (Baltimore). Increased Serum Levels of Macrophage Inflammatory Protein-3α and Cystatin A Predict a Poor Prognosis of Nasopharyngeal Carcinoma [Pubmed:25396333]
Cancer Serum chemokine network correlates with chemotherapy in non-small cell lung cancer [PubMed: 25976768]
American Journal of Cancer Research CCR6+ B lymphocytes responding to tumor cell-derived CCL20 support hepatocellular carcinoma progression via enhancing angiogenesis. [pubmed:28560063]
Biological Research In vitro chemokine (CC motif) receptor 6-dependent non-inflammatory chemotaxis during spermatogenesis [10.1186:s40659-018-0161-z]
BioMed Research International Indoleamine 2, 3-Dioxygenase (IDO) Regulates Th17/Treg Immunity in Experimental IgA Nephropathy []
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