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CXCL12 ELISA Kit

Maus CXCL12 ELISA-Kit Colorimetric-Assay zur Quantifizierung von Maus CXCL12 und wurde in 4+ Publikationen erwähnt.
Produktnummer ABIN2859208

Kurzübersicht für CXCL12 ELISA Kit (ABIN2859208)

Target

Alle CXCL12 ELISA Kits anzeigen
CXCL12 (Chemokine (C-X-C Motif) Ligand 12 (CXCL12))

Bindungsspezifität

AA 22-93

Reaktivität

  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Maus

Nachweismethode

Colorimetric

Methodentyp

Sandwich ELISA

Detektionsbereich

62.5-4000 pg/mL

Applikation

ELISA

Proben

Cell Culture Supernatant, Serum, Plasma (heparin)
  • Untere Nachweisgrenze

    62.5 pg/mL

    Verwendungszweck

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

    Marke

    PicoKine™

    Analytische Methode

    Quantitative

    Spezifität

    Natural and recombinant mouse SDF-1

    Kreuzreaktivität (Details)

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

    Sensitivität

    <10pg/mL

    Bestandteile

    • 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

    Immunogen

    Expression system for standard: E.coli
    Immunogen sequence: K22-M93
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Plattentyp

    Pre-coated

    Protokoll

    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.

    Testdurchführung

    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.

    Testpräzision

    • 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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Lagerung

    -20 °C,4 °C

    Informationen zur Lagerung

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

    Haltbarkeit

    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).

  • Target Alle CXCL12 ELISA Kits anzeigen

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

    Andere Bezeichnung

    CXCL12

    Hintergrund

    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.

    Gen-ID

    20315

    UniProt

    H7BX38

    Pathways

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