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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 產品包裝(模擬)
  • 巨噬細胞炎性蛋白3β(MIP3b)活性蛋白 產品包裝(模擬)
  • APA096Hu01.png Figure. 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

避免反復凍融。2-8°C不超過一個月,-80°C不超過12個月。

穩定性

熱穩定性以損失率顯示。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生。保質期內,在適當的條件下存儲,損失率低于5%。

相關產品

編號 適用物種:Homo sapiens (Human,人) 應用(僅供研究使用,不用于臨床診斷!)
URPA096Hu01 巨噬細胞炎性蛋白3β(MIP3b)重組蛋白 Positive Control; Immunogen; SDS-PAGE; WB.
UAPA096Hu01 巨噬細胞炎性蛋白3β(MIP3b)活性蛋白 Cell?culture;?Activity?Assays.
UPAA096Hu01 巨噬細胞炎性蛋白3β(MIP3b)多克隆抗體 WB; IHC; ICC/IF
ULAA096Hu71 巨噬細胞炎性蛋白3β(MIP3b)多克隆抗體(生物素標記) WB
UMAA096Hu22 巨噬細胞炎性蛋白3β(MIP3b)單克隆抗體 WB; IHC; ICC; IP.
USEA096Hu 巨噬細胞炎性蛋白3β(MIP3b)檢測試劑盒(酶聯免疫吸附試驗法) Enzyme-linked immunosorbent assay for Antigen Detection.
ULMA096Hu 巨噬細胞炎性蛋白3β(MIP3b)等多因子檢測試劑盒(流式熒光發光法) FLIA Kit for Antigen Detection.

參考文獻

雜志 參考文獻
BMC Veterinary Research MIP-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 Immunity Plasma inflammatory biomarkers for Huntington’s disease patients and mouse model [Pubmed:25266150]
Brain, Behavior, and Immunity Plasma inflammatory biomarkers for Huntington’s disease patients and mouse model [PubMed: 25266150]
類風濕關節炎血清中CCL19 和CCL21 的表達水平與肺間質病變的關系 [:]
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