LGALS1/Galectin 1 ELISA Kit
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- Target See all LGALS1/Galectin 1 (LGALS1) ELISA Kits
- LGALS1/Galectin 1 (LGALS1) (Lectin, Galactoside-Binding, Soluble, 1 (LGALS1))
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Reactivity
- Mouse
- Detection Method
- Colorimetric
- Method Type
- Sandwich ELISA
- Detection Range
- 156-10000 pg/mL
- Minimum Detection Limit
- 156 pg/mL
- Application
- ELISA
- Purpose
- For quantitative detection of Galectin-1 in mouse serum, plasma, body fluids, tissue lysates or cell culture supernatants.
- Sample Type
- Cell Culture Supernatant, Plasma, Serum, Tissue Lysate
- Analytical Method
- Quantitative
- Sensitivity
- < 5 pg/mL
- Components
- 1. One 96-well plate pre-coated with anti-Mouse Galectin-1 antibody 2. Lyophilized Mouse Galectin-1 standards: 2 tubes (10ng / tube) 3. Sample / Standard diluent buffer: 30ml 4. Biotin conjugated anti-Mouse Galectin-1 antibody (Concentrated): 130 µl.
- Material not included
- 1. 37 °C incubator 2. Microplate reader (wavelength: 450nm) 3. Precise pipette and disposable pipette tips 4. Automated plate washer 5. ELISA shaker 6. 1.5ml of Eppendorf tubes 7. Plate cover 8. Absorbent filter papers 9. Plastic or glass container with volume of above 1L
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- Comment
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This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti- Galectin-1 polyclonal antibody was pre-coated onto 96-well plates. And the biotin conjugated anti-GALECTIN-1 polyclonal antibody was used as detection antibodies. The standards test samples and biotin conjugated detection antibody were added - the wells subsequently and wash with wash buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with wash buffer. TMB substrates were used - visualize HRP enzymatic reaction. TMB was catalyzed by HRP - produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional - the Galectin-1 amount of sample captured in plate. Read the O.D. absorbance at 450 nm in a microplate reader and then the concentration of Galectin-1 can be calculated.
- Plate
- Pre-coated
- Reagent Preparation
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- Before the experiment, centrifuge each kit component for several minutes to bring down all reagents to the bottom of tubes. 2. It is recommend to measure each standard and sample in duplicate. 3. Do NOT let the plate completely dry at any time! Since the dry condition can inactivate the biological material on the plate. 4. Do not reuse pipette tips and tubes to avoid cross contamination. 5. Do not use the expired components and the components from different batches. 6. To avoid the marginal effect of plate incubation for temperature differences (the marginal wells always get stronger reaction), it is recommend to equilibrate the ABC working solution and TMB substrate for at least 30 min at room temperature (37°C ) before adding to wells.The TMB substrate (Kit Component 8) is colorless and transparent before use, if not, please contact us for replacement.
- Sample Preparation
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Preparation of sample and reagents 1. Sample Isolate the test samples soon after collecting, then, analyze immediately (within 2 hours). Or aliquot and store at -20 °C for long term. Avoid multiple freeze-thaw cycles.
Cell culture supernatants: Centrifuge to remove precipitate, analyze immediately or aliquot and store at -20 °C .
Body fluids and tissue lysates: Centrifuge at approximately 2000 X g for 20 min to remove precipitate.
Serum: Coagulate the serum at room temperature (about 4 hours). Centrifuge at approximately 2000 × g for 20 min. Analyze the serum immediately or aliquot and store at -20 °C .
Plasma: Collect plasma with heparin or EDTA as the anticoagulant. Centrifuge for 20 min at 2000 x g within 30 min of collection. Analyze immediately or aliquot and store frozen at -20 °C. Citrate can not be used as anticoagulant here. Note: 1. Coagulate blood samples completely, then, centrifuge, and avoid hemolysis and particle. 2. NaN3 can not be used as test sample preservative, since it is the inhibitor for HRP. - Restrictions
- For Research Use only
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- Preservative
- Sodium azide, Thimerosal (Merthiolate)
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- Target See all LGALS1/Galectin 1 (LGALS1) ELISA Kits
- LGALS1/Galectin 1 (LGALS1) (Lectin, Galactoside-Binding, Soluble, 1 (LGALS1))
- Alternative Name
- Galectin-1 (LGALS1 Products)
- Synonyms
- GAL1 ELISA Kit, GBP ELISA Kit, Galectin-1 ELISA Kit, LGAS1 ELISA Kit, LGALS1 ELISA Kit, MGC64502 ELISA Kit, GB10026 ELISA Kit, AA410090 ELISA Kit, Gal-1 ELISA Kit, Galbp ELISA Kit, L-14.5 ELISA Kit, L14 ELISA Kit, Lect14 ELISA Kit, galectin-1 ELISA Kit, Galaptin ELISA Kit, galectin 1 ELISA Kit, galectin-1 ELISA Kit, lectin, galactoside-binding, soluble, 1 L homeolog ELISA Kit, protein enabled ELISA Kit, lectin, galactose binding, soluble 1 ELISA Kit, LGALS1 ELISA Kit, Lgals1 ELISA Kit, CC1G_05003 ELISA Kit, CC1G_05004 ELISA Kit, lgals1.L ELISA Kit, LOC408848 ELISA Kit
- Background
- Galectin-1 is a member of the galectins, which are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. In Mouses it is encoded by the LGALS1 gene, which maps to 22q12-q13. It is expressed by the endometrial stromal cells throughout the menstrual cycle, however significantly increases during implantation. The Galectin-a plays a role in the immunosuppression required for a successful pregnancy, and it may also act as an autocrine negative growth factor that regulates cell proliferation.
- Pathways
- Carbohydrate Homeostasis
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