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巨噬細(xì)胞炎性蛋白1α(MIP1a)活性蛋白

Active Macrophage Inflammatory Protein 1 Alpha (MIP1a)

CCL3; MIP1-A; SCYA3; Chemokine C-C-Motif Ligand 3; Small Inducible Cytokine A3; Homologous To Mouse Mip-1a; Tonsillar Lymphocyte LD78 Alpha Protein

  • 巨噬細(xì)胞炎性蛋白1α(MIP1a)活性蛋白 產(chǎn)品包裝(模擬)
  • 巨噬細(xì)胞炎性蛋白1α(MIP1a)活性蛋白 產(chǎn)品包裝(模擬)
  • 巨噬細(xì)胞炎性蛋白1α(MIP1a)活性蛋白 Gene sequencing
  • APA092Hu61.jpg SDS-PAGE圖
  • 巨噬細(xì)胞炎性蛋白1α(MIP1a)活性蛋白 Figure. Western Blot; Sample: APA092Hu61; Antibody: PAA092Hu06.
  • Certificate 通過ISO 9001、ISO 13485質(zhì)量體系認(rèn)證

活性實(shí)驗(yàn)

MIP-1a (macrophage inflammatory protein 1-alpha) also known as Chemokine (C-C motief) ligand 3 (CCL3), is a cytokine belonging to the CC chemokine family that is involved in the recruitment and activation of macrophages, monocytes and neutrophils. In this case, chemotaxis?assay used 24-well microchemotaxis system was undertaken to evaluate the chemotactic effect of MIP-1a on the human monocytic cell line THP1. Briefly, THP1 cells were seeded into the upper chambers (100μl cell suspension, 106 cells/ml in RPMI 1640 with 0.5% FBS) and MIP-1a (100ng/mL, diluted 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 37oC with 5% CO2 for 5h, the filter was removed, then cells in low chamber were observed by inverted microscope at low magnification (×40) and the number of migrated cells were counted at high magnification (×400) randomly (five fields for each filter).
By counting migrated cells in low chamber at high magnification (×400) randomly, it was shown that a mean of 41.2 THP1 cells/field migrated towards serum free RPMI 1640 medium with 100ng/mL MIP-1a, while only 3.6 THP1 cells/field migrated towards serum free RPMI 1640 medium. And the migrated THP1 cells in low chamber at low magnification (×40) was shown in Figure 1.

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(gè)月,-80°C不超過12個(gè)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(yàn)決定,具體方法如下:在37°C孵育48小時(shí),沒有顯著的降解或者沉淀產(chǎn)生。保質(zhì)期內(nèi),在適當(dāng)?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!)
RPA092Hu01 巨噬細(xì)胞炎性蛋白1α(MIP1a)重組蛋白 Positive Control; Immunogen; SDS-PAGE; WB.
APA092Hu01 巨噬細(xì)胞炎性蛋白1α(MIP1a)活性蛋白 Cell?culture;?Activity?Assays.
APA092Hu61 巨噬細(xì)胞炎性蛋白1α(MIP1a)活性蛋白 Cell?culture;?Activity?Assays.
EPA092Hu61 巨噬細(xì)胞炎性蛋白1α(MIP1a)真核蛋白 Positive Control; Immunogen; SDS-PAGE; WB.
EPA092Hu51 巨噬細(xì)胞炎性蛋白1α(MIP1a)真核蛋白 Positive Control; Immunogen; SDS-PAGE; WB.
PAA092Hu07 巨噬細(xì)胞炎性蛋白1α(MIP1a)多克隆抗體 WB; IHC; ICC; IP.
PAA092Hu01 巨噬細(xì)胞炎性蛋白1α(MIP1a)多克隆抗體 WB; IHC; ICC; IP.
PAA092Hu06 巨噬細(xì)胞炎性蛋白1α(MIP1a)多克隆抗體 WB; IHC; ICC; IP.
MAA092Hu22 巨噬細(xì)胞炎性蛋白1α(MIP1a)單克隆抗體 WB; IHC; ICC; IP.
SEA092Hu 巨噬細(xì)胞炎性蛋白1α(MIP1a)檢測試劑盒(酶聯(lián)免疫吸附試驗(yàn)法) Enzyme-linked immunosorbent assay for Antigen Detection.
SCA092Hu 巨噬細(xì)胞炎性蛋白1α(MIP1a)檢測試劑盒(化學(xué)發(fā)光免疫分析法) Chemiluminescent immunoassay for Antigen Detection.
LMA092Hu 巨噬細(xì)胞炎性蛋白1α(MIP1a)等多因子檢測試劑盒(流式熒光發(fā)光法) FLIA Kit for Antigen Detection.
KSA092Hu01 巨噬細(xì)胞炎性蛋白1α(MIP1a)檢測試劑盒DIY材料(酶聯(lián)免疫吸附試驗(yàn)法) Main materials for "Do It (ELISA Kit) Yourself".
PGA092Hu01 巨噬細(xì)胞炎性蛋白1α(MIP1a)引物對 PCR

參考文獻(xiàn)

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