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巨噬細胞炎性蛋白3β(MIP3b)活性蛋白

Active Macrophage Inflammatory Protein 3 Beta (MIP3b)

CCL19; CKb11; ELC; MIP3-B; SCYA19; Chemokine C-C-Motif Ligand 19; Beta Chemokine Exodus-3; CK Beta-11; EBI1-Ligand Chemokine; Small Inducible Cytokine Subfamily A19

  • 巨噬細胞炎性蛋白3β(MIP3b)活性蛋白產(chǎn)品包裝(模擬)
  • 巨噬細胞炎性蛋白3β(MIP3b)活性蛋白產(chǎn)品包裝(模擬)
  • APA096Hu01.pngFigure. SDS-PAGE
  • 巨噬細胞炎性蛋白3β(MIP3b)活性蛋白Sample: Recombinant MIP3b, Human;
    Antibody: Rabbit Anti-Human MIP3b Ab (PAA096Hu01)
    Figure. Western Blot
  • Certificate通過ISO 9001、ISO 13485質(zhì)量體系認證

活性實驗

Macrophage Inflammatory Protein 3 Beta (MIP3b) is a small cytokine belonging to the CC chemokine family that is also known as EBI1 ligand chemokine (ELC) and Chemokine C-C motif ligand 19 (CCL19). This chemokine elicits its effects on its target cells by binding to the chemokine receptor 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 MIP3b on the Jurkat cell line. Briefly, Jurkat cells were seeded into the upper chambers (150μL cell suspension,106 cells/mL in RPMI 1640 with FBS free) and MIP3b (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 (8μm pore size) used to separate the two compartments. After incubation at 37℃ with 5% CO2 for 3h, 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 MIP3b 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 MIP3b occurs at 0.1-1ng/mL.
(A) Jurkat cells were seeded into the upper chambers and serum free RPMI 1640 with 0.1ng/mL MIP3b was added in lower chamber, then cells in lower chamber were observed at low magnification (×100) after incubation for 3h;
(B) Jurkat cells were seeded into the upper chambers and serum free RPMI 1640 without MIP3b was added in lower chamber, then cells in lower chamber were observed at low magnification (×100) after incubation for 3h.
Figure. The chemotactic effect of recombinant human MIP3b on Jurkat cells.

Figure. The chemotactic effect of recombinant human MIP3b on Jurkat cells.

用法

Reconstitute in 20mM Tris, 150mM NaCl (PH8.0) to a concentration of 0.1-1.0 mg/mL. Do not vortex.

儲存

避免反復(fù)凍融。2-8°C不超過一個月,-80°C不超過12個月。

穩(wěn)定性

熱穩(wěn)定性以損失率顯示。損失率是由加速降解試驗決定,具體方法如下:在37°C孵育48小時,沒有顯著的降解或者沉淀產(chǎn)生。保質(zhì)期內(nèi),在適當?shù)臈l件下存儲,損失率低于5%。

相關(guān)產(chǎn)品

編號適用物種:Homo sapiens (Human,人)應(yīng)用(僅供研究使用,不用于臨床診斷!)
RPA096Hu01巨噬細胞炎性蛋白3β(MIP3b)重組蛋白Positive Control; Immunogen; SDS-PAGE; WB.
APA096Hu01巨噬細胞炎性蛋白3β(MIP3b)活性蛋白Cell?culture;?Activity?Assays.
PAA096Hu01巨噬細胞炎性蛋白3β(MIP3b)多克隆抗體WB,IHC,ICC/IF
LAA096Hu71巨噬細胞炎性蛋白3β(MIP3b)多克隆抗體(生物素標記)WB
MAA096Hu22巨噬細胞炎性蛋白3β(MIP3b)單克隆抗體WB; IHC; ICC; IP.
SEA096Hu巨噬細胞炎性蛋白3β(MIP3b)檢測試劑盒(酶聯(lián)免疫吸附試驗法)Enzyme-linked immunosorbent assay for Antigen Detection.
LMA096Hu巨噬細胞炎性蛋白3β(MIP3b)等多因子檢測試劑盒(流式熒光發(fā)光法)FLIA Kit for Antigen Detection.

參考文獻

雜志參考文獻
BMC Veterinary ResearchMIP-3beta/CCL19 is associated with the intrathecal invasion of mononuclear cells in neuroinflammatory and non-neuroinflammatory CNS diseases in dogs[Pubmed:25016392]
Brain, Behavior, and ImmunityPlasma inflammatory biomarkers for Huntington’s disease patients and mouse model [Pubmed:25266150]
Brain, Behavior, and ImmunityPlasma inflammatory biomarkers for Huntington’s disease patients and mouse model[PubMed: 25266150]
類風濕關(guān)節(jié)炎血清中CCL19 和CCL21 的表達水平與肺間質(zhì)病變的關(guān)系[:]