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CXCL12 ELISA 试剂盒

This 小鼠 CXCL12 ELISA Kit is a Colorimetric ELISA Kit designed to quantify 小鼠 CXCL12. This ELISA Kit has been cited in 4+ publications.
产品编号 ABIN2859208
发货至: 中国

Quick Overview for CXCL12 ELISA 试剂盒 (ABIN2859208)

抗原

See all CXCL12 ELISA试剂盒
CXCL12 (Chemokine (C-X-C Motif) Ligand 12 (CXCL12))

抗原表位

AA 22-93

适用

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小鼠

检测方法

Colorimetric

实验类型

Sandwich ELISA

检测范围

62.5-4000 pg/mL

应用范围

ELISA

样品类型

Cell Culture Supernatant, Serum, Plasma (heparin)
  • 最低检测浓度

    62.5 pg/mL

    原理

    For quantitative detection of mouse SDF-1 in cell culture supernates, serum and plasma(heparin).

    品牌

    PicoKine™

    Analytical Method

    Quantitative

    特异性

    Natural and recombinant mouse SDF-1

    交叉反应 (详细)

    There is no detectable cross-reactivity with other relevant proteins.

    灵敏度

    <10pg/mL

    组件

    • 96-well plate precoated with anti- mouse SDF-1 antibod - 1
    • Lyophilized recombinant mouse SDF-1 standar - 10ng/tubex2
    • Biotinylated anti- mouse SDF-1 antibod - 130ul(dilution 1:100)
    • Avidin-Biotin-Peroxidase Complex(ABC - 130ul(dilution 1:100)
    • Sample diluent buffe - 30ml
    • Antibody diluent buffe - 12ml
    • ABC diluent buffe - 12ml
    • TMB color developing agen - 10ml
    • TMB stop solutio - 10ml

    免疫原

    Expression system for standard: E.coli
    Immunogen sequence: K22-M93
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    板类型

    Pre-coated

    实验流程

    mouse SDF-1 ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from rat specific for SDF-1 has been precoated onto 96-well plates. Standards(E.coli, K22-M93) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for SDF-1 is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with PBS or TBS buffer. HRP substrate TMB was used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the mouse SDF-1 amount of sample captured in plate.

    实验流程

    Aliquot 0.1 mL per well of the 4000pg/mL, 2000pg/mL, 1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL mouse SDF-1 standard solutions into the precoated 96-well plate. Add 0.1 mL of the sample diluent buffer into the control well (Zero well). Add 0.1 mL of each properly diluted sample of mouse cell culture supernates, serum or plasma(heparin) to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each mouse SDF-1 standard solution and each sample be measured in duplicate.

    实验精密度

    • Sample 1: n=16, Mean(ng/ml): 0.67, Standard deviation: 0.027, CV(%): 4
    • Sample 2: n=16, Mean(ng/ml): 1.6, Standard deviation: 0.056, CV(%): 3.5
    • Sample 3: n=16, Mean(ng/ml): 2.8, Standard deviation: 0.126, CV(%): 4.5,
    • Sample 1: n=24, Mean(ng/ml): 0.91, Standard deviation: 0.053, CV(%): 5.8
    • Sample 2: n=24, Mean(ng/ml): 2.1, Standard deviation: 0.107, CV(%): 5.4
    • Sample 3: n=24, Mean(ng/ml): 3.2, Standard deviation: 0.202, CV(%): 6.3

    限制

    仅限研究用
  • 储存条件

    -20 °C,4 °C

    储存方法

    Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles

    有效期

    12 months
  • Zhang, Teng, Liu, Zhang, Liu: "Gene expression profile analyze the molecular mechanism of CXCR7 regulating papillary thyroid carcinoma growth and metastasis." in: Journal of experimental & clinical cancer research : CR, Vol. 34, pp. 16, (2015) (PubMed).

    Wu, Li, Wang, Shen, Xu, Liu, Zhuo, Xia, Gao, Tan: "Ultrasound-targeted stromal cell-derived factor-1-loaded microbubble destruction promotes mesenchymal stem cell homing to kidneys in diabetic nephropathy rats." in: International journal of nanomedicine, Vol. 9, pp. 5639-51, (2014) (PubMed).

    Lin, Han, Wang, Xu, Yu, Yang: "CXCR7 stimulates MAPK signaling to regulate hepatocellular carcinoma progression." in: Cell death & disease, Vol. 5, pp. e1488, (2014) (PubMed).

    Tong, Ding, Shen, Chen, Bian, Ma, Yao, Yang: "Mesenchymal stem cell transplantation enhancement in myocardial infarction rat model under ultrasound combined with nitric oxide microbubbles." in: PLoS ONE, Vol. 8, Issue 11, pp. e80186, (2013) (PubMed).

  • 抗原 See all CXCL12 ELISA试剂盒

    CXCL12 (Chemokine (C-X-C Motif) Ligand 12 (CXCL12))

    别名

    CXCL12

    背景

    SDF-1(stromal cell-derived factor-1) is small cytokine belonging to the chemokine family that is officially designated Chemokine(C-X-C motif) ligand 12(CXCL12). This gene is located on chromosome 10q11.1. SDF-1 is produced in two forms, SDF-1alpha/CXCL12a and SDF-1beta/CXCL12b, by alternate splicing of the same gene. Chemokines are characterized by the presence of four conserved cysteines, which form two disulfide bonds. The CXCL12 proteins belong to the group of CXC chemokines, whose initial pair of cysteines are separated by one intervening amino acid. CXCL12 is strongly chemotactic for lymphocytes. CXCL12 was shown to be expressed in many tissues in mice(including brain, thymus, heart, lung, liver, kidney, spleen and bone marrow). CXCL12 is a highly efficacious lymphocyte chemoattractant. In addition, CXCL12 induces intracellular actin polymerization in lymphocytes. CXCL12 is a substrate for the matrix metalloproteinase-2, which cleaves an CXCL12 N-terminal tetrapeptide. The standard product used in this kit is recombinant SDF-1 with the molecular mass of 8Kda.

    基因ID

    20315

    UniProt

    H7BX38

    途径

    Regulation of Cell Size, CXCR4-mediated Signaling Events, Negative Regulation of intrinsic apoptotic Signaling
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