CXCL12 ELISA Kit

Produktnummer ABIN416336

Dieses Colorimetric ELISA kit dient der quantitativen Messung von Ratte CXCL12. Es wurde in 12 Publikationen zitiert.

Kurzübersicht für CXCL12 ELISA Kit (ABIN416336)

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

Reaktivität: Ratte

Nachweismethode: Colorimetric

Methodentyp: Sandwich ELISA

Detektionsbereich: 0.156 ng/mL - 10 ng/mL

Applikation: ELISA

Proben: Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate

Produktdetails CXCL12 ELISA Kit

Untere Nachweisgrenze: 0.156 ng/mL

Verwendungszweck: The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of SDF1 in Serum,Plasma,Tissue Homogenate,Cell Lysate,Cell Culture Supernatant,Biological Fluids

Analytische Methode: Quantitative

Spezifität:

This assay has high sensitivity and excellent specificity for detection of Stromal Cell Derived Factor 1 (SDF1).
No significant cross-reactivity or interference between Stromal Cell Derived Factor 1 (SDF1) and analogues was observed.

Kreuzreaktivität (Details): No significant cross-reactivity or interference between Stromal Cell Derived Factor 1 (SDF1) and analogues was observed.

Sensitivität: < 0.055 ng/mL

Bestandteile:

• Pre-coated, 96-well strip plate
• Plate sealer
• Standard
• Standard Diluent
• Detection Reagent A
• Assay Diluent A
• Detection Reagent B
• Assay Diluent B
• TMB Substrate
• Stop Solution
• Wash Buffer (30X)
• Instruction manual

Benötigtes Material:

• Microplate reader with 450 nm filter.
• Precision single or multi-channel pipettes and disposable tips.
• Eppendorf Tubes for diluting samples.
• Deionized or distilled water.
• Absorbent paper for blotting the microtiter plate.
• Container for Wash Solution

Anwendungsinformationen

Applikationshinweise:

• Limited by the current condition and scientific technology, we cannot completely conduct the comprehensive identification and analysis on the raw material provided by suppliers. So there might be some qualitative and technical risks to use the kit.
• The final experimental results will be closely related to validity of the products, operation skills of the end users and the experimental environments. Please make sure that sufficient samples are available.
• Kits from different batches may be a little different in detection range, sensitivity and color developing time.
• Do not mix or substitute reagents from one kit lot to another. Use only the reagents supplied by manufacturer.
• Protect all reagents from strong light during storage and incubation. All the bottle caps of reagents should be covered tightly to prevent the evaporation and contamination of microorganism.
• There may be some foggy substance in the wells when the plate is opened at the first time. It will not have any effect on the final assay results. Do not remove microtiter plate from the storage bag until needed.
• Wrong operations during the reagents preparation and loading, as well as incorrect parameter setting for the plate reader may lead to incorrect results. A microplate plate reader with a bandwidth of 10nm or less and an optical density range of 0-3 O.D. or greater at 450 ± 10nm wavelength is acceptable for use in absorbance measurement. Please read the instruction carefully and adjust the instrument prior to the experiment.
• Even the same operator might get different results in two separate experiments. In order to get better reproducible results, the operation of every step in the assay should be controlled. Furthermore, a preliminary experiment before assay for each batch is recommended.
• Each kit has been strictly passed Q.C test. However, results from end users might be inconsistent with our in-house data due to some unexpected transportation conditions or different lab equipments. Intra-assay variance among kits from different batches might arise from above factors, too.
• Kits from different manufacturers for the same item might produce different results, since we have not compared our products with other manufacturers.

Kommentare:

Information on standard material:
The standard might be recombinant protein or natural protein, that will depend on the specific kit. Moreover, the expression system is E.coli or yeast or mammal cell. There is 0.05% proclin 300 in the standard as preservative.

Information on reagents:
The stop solution used in the kit is sulfuric acid with concentration of 1 mol/L. And the wash solution is TBS. The standard diluent contains 0.02 % sodium azide, assay diluent A and assay diluent B contain 0.01% sodium azide. Some kits can contain is BSA in them.

Information on antibodies:
The provided antibodies and their host vary in different kits.

Probenmenge: 100 μL

Testdauer: 3 h

Plattentyp: Pre-coated

Protokoll: 1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 2 hours at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
8. Add 50µL Stop Solution. Read at 450nm immediately.

Testpräzision:

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Stromal Cell Derived Factor 1 (SDF1) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Stromal Cell Derived Factor 1 (SDF1) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Vorsichtsmaßnahmen: The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.

Handhabung: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5 % within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

Lagerung: 4 °C

Informationen zur Lagerung:

• For unopened kit: All the reagents should be kept according to the labels on vials. The Standard, Detection Reagent A, Detection Reagent B and the 96-well strip plate should be stored at -20°C upon receipt while the others should be at 4°C.
• For opened kit: When the kit is opened, the remaining reagents still need to be stored according to the above storage condition. Besides, please return the unused wells to the foil pouch containing the desiccant pack, and reseal along entire edge of zip-seal.
  Note: It is highly recommended to use the remaining reagents within 1 month provided this is within the expiration date of the kit.
• For ELISA kit, 1 day storage at 37°C can be considered as 2 months at 4°C, which means 3 days at 37°C equaling 6 months at 4°C.

Haltbarkeit: 6 months

Referenzen für CXCL12 ELISA Kit (ABIN416336)

Golle, Gerth, Beul, Heitplatz, Barth, Fobker, Pavenstädt, Di Marco, Brand: "Bone marrow-derived cells and their conditioned medium induce microvascular repair in uremic rats by stimulation of endogenous repair mechanisms." in: Scientific reports, Vol. 7, Issue 1, pp. 9444, (2019) (PubMed).

Wu, Cao, Liu, Zheng, Jiao, Zeng, Wang, Kaplan, Jiang: "Functionalization of Silk Fibroin Electrospun Scaffolds via BMSC Affinity Peptide Grafting through Oxidative Self-Polymerization of Dopamine for Bone Regeneration." in: ACS applied materials & interfaces, Vol. 11, Issue 9, pp. 8878-8895, (2019) (PubMed).

Ying, Wen, Pei, Su, Ruan: "Stromal cell-derived factor-1α promotes recruitment and differentiation of nucleus pulposus-derived stem cells." in: World journal of stem cells, Vol. 11, Issue 3, pp. 196-211, (2019) (PubMed).

Shen, Chen, Gu, Ning, Zeng, Yi, Lu: "AMD3100 treatment attenuates pulmonary angiogenesis by reducing the c-kit (+) cells and its pro-angiogenic activity in CBDL rat lungs." in: Biochimica et biophysica acta. Molecular basis of disease, Vol. 1864, Issue 3, pp. 676-684, (2018) (PubMed).

Eibel, Kristochek, Peres, Dias, Dartora, Casali, Kalil, Lehnen, Irigoyen, Markoski: "β-blockers interfere with cell homing receptors and regulatory proteins in a model of spontaneously hypertensive rats." in: Cardiovascular therapeutics, Vol. 36, Issue 4, pp. e12434, (2018) (PubMed).

Zhou, Xu, Wang, Lin, Liu, He: "The effects of Sr-incorporated micro/nano rough titanium surface on rBMSC migration and osteogenic differentiation for rapid osteointegration." in: Biomaterials science, Vol. 6, Issue 7, pp. 1946-1961, (2018) (PubMed).

García-Marchena, Araos, Barrios, Sánchez-Marín, Chowen, Pedraz, Castilla-Ortega, Romero-Sanchiz, Ponce, Gavito, Decara, Silva, Torrens, Argente, Rubio, Serrano, de Fonseca, Pavón: "Plasma Chemokines in Patients with Alcohol Use Disorders: Association of CCL11 (Eotaxin-1) with Psychiatric Comorbidity." in: Frontiers in psychiatry, Vol. 7, pp. 214, (2017) (PubMed).

Wu, Ji, Wang, Nan, Liu: "Stromal cell-derived factor 1 promoted migration of adipose-derived stem cells to the wounded area in traumatic rats." in: Biochemical and biophysical research communications, Vol. 467, Issue 1, pp. 140-5, (2015) (PubMed).

Guo, Chai, Chen, Chen, Ge, Li, Li, Li, Cao: "Stromal cell-derived factor 1 (SDF-1) accelerated skin wound healing by promoting the migration and proliferation of epidermal stem cells." in: In vitro cellular & developmental biology. Animal, Vol. 51, Issue 6, pp. 578-85, (2015) (PubMed).

Shao, Cai, Sheng, Yin: "Role of SDF-1 and Wnt signaling pathway in the myocardial fibrosis of hypertensive rats." in: American journal of translational research, Vol. 7, Issue 8, pp. 1345-56, (2015) (PubMed).

Uchinaka, Kawaguchi, Mori, Hamada, Miyagawa, Saito, Sawa, Matsuura: "Tissue inhibitor of metalloproteinase-1 and -3 improves cardiac function in an ischemic cardiomyopathy model rat." in: Tissue engineering. Part A, Vol. 20, Issue 21-22, pp. 3073-84, (2014) (PubMed).

Tong, Xu, Han, Chen, Yang, Qiao, Hong, Wu, Zhou et al.: "Tanshinone IIA increases recruitment of bone marrow mesenchymal stem cells to infarct region via up-regulating stromal cell-derived factor-1/CXC chemokine receptor 4 axis in a myocardial ischemia ..." in: Phytomedicine : international journal of phytotherapy and phytopharmacology, Vol. 18, Issue 6, pp. 443-50, (2011) (PubMed).

Details zu CXCL12

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

Andere Bezeichnung: SDF1

Hintergrund: CXCL12, PBSF, P-BSF, SCYB12, SDF1-A, SDF1-B, SDF1A, SDF1B, TLSF-A, TLSF-B, TPAR1, Pre-B Cell Growth-Stimulating Factor, Chemokine C-X-C-Motif Ligand 12

UniProt: Q9QZD1

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