Rat TGFB1 ELISA Kit, Lot 21AO-1115 [Cancer Immune Checkpoint Assay Kit]

CAT#: IOK-05-P1026
Product Type: ELISA Kit
Target: TGFB1
Short Description
The kit is designed for in vitro quantitative measurement of Rat TGFB1 in Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate.
Description
The kit is a sandwich enzyme immunoassay for the in vitro quantitative measurement of TGFb1 in rat serum, platelet-poor plasma, tissue homogenates, cell culture supernates and other biological fluids.
Applications
ELISA
Target
TGFB1
Reactivity
Rat
Detection Method
Colorimetric
Method Type
Sandwich ELISA
Analytical Method
Quantitative
Sample Type
Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Specificity
This assay has high sensitivity and excellent specificity for detection of this index.
Cross-Reactivity
No significant cross-reactivity or interference between this index and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between this index and all the analogues, therefore, cross reaction may still exist.
Components
Pre-coated, ready to use 96-well strip plate
Plate sealer for 96 wells
Standard
Standard Diluent
Detection Reagent A
Detection Reagent B
Assay Diluent A
Assay Diluent B
TMB Substrate
Stop Solution
Wash Buffer (30 x concentrate)
Instruction manual
Material not included
1.Microplate reader with 450 ± 10nm filter.
2.Precision single or multi-channel pipettes and disposable tips.
3.Tubes for diluting samples.
4.Deionized or distilled water.
5.Absorbent paper for blotting the microtiter plate.
6.Container for Wash Solution.
7.0.01Mol/L (or 1x) Phosphate Buffered Saline(PBS), pH 7.0-7.2.
Sensitivity
13.3 pg/mL
Sample Volume
100 μL
Assay Time
1 - 4.5 h
Plate
Pre-coated
Assay Procedure
The microtiter plate provided in this kit has been pre-coated with an antibody specific to the index. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific to the index. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain the index, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm.
Assay Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level of target were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level of target were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV < 10%
Inter-Assay: CV < 12%
Precaution of Use
The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
Handling Advice
The stability of ELISA 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 conditions. Note: To minimize unnecessary influences on the performance, operation procedures and lab conditions, especially room temperature, air humidity and incubator temperatures should be strictly regulated.
Storage
4 °C,-20 °C
Storage Comment
The Assay Plate, Standard, Detection Reagent A and Detection Reagent B should be stored at -20°C upon being received. After receiving the kit , Substrate should be always stored at 4°C.Other reagents are kept according to the labels on vials. But for long term storage, please keep the whole kit at -20°C. The unused strips should be kept in a sealed bag with the desiccant provided to minimize exposure to damp air.
Expiry Date
12 months
Note
The Assay Plate, Standard, Detection Reagent A and Detection Reagent B should be stored at -20°C upon being received. After receiving the kit , Substrate should be always stored at 4°C.Other reagents are kept according to the labels on vials. But for long term storage, please keep the whole kit at -20°C. The unused strips should be kept in a sealed bag with the desiccant provided to minimize exposure to damp air.
Restrictions
For Research Use only
Alternative Name
Transforming Growth factor beta1
Synonyms
CED; DPD1; LAP; TGFB; TGFbeta; TGF-beta; TGF-BETA-1; TGF-beta5; ced; dpd1; lap; tgf-beta; tgfb; tgfb5; tgfbeta; TGF-beta1; TGFbeta1; Tgfb; Tgfb-1; ai39657; tgfb1; wu:fb13a07; xx:ai39657; TGFB1; csd; cdb1; cdg2; csd1; csd2; csd3; ebmd; lcd1; bigh3; cdgg1; betaig-h3; TGFB4; transforming growth factor beta 1; transforming growth factor beta-1; transforming growth factor beta 1 L homeolog; transforming growth factor; beta 1; transforming growth factor; beta 1a; transforming growth factor beta induced L homeolog; TGFB1; Tgfb1; tgfb1.L; tgfb1a; tgfbi.L
Background
Alternative name: TGF-B1, CED, DPD1, LAP, Camurati-Engelmann Disease, Latency-associated peptide
Gene ID
59086
UniProt
P17246
Pathways
EGFR Signaling Pathway, Dopaminergic Neurogenesis, Cellular Response to Molecule of Bacterial Origin, Glycosaminoglycan Metabolic Process, Regulation of Leukocyte Mediated Immunity, Regulation of Muscle Cell Differentiation, Positive Regulation of Immune Effector Process, Cell-Cell Junction Organization, Production of Molecular Mediator of Immune Response, Ribonucleoside Biosynthetic Process, Skeletal Muscle Fiber Development, Regulation of Carbohydrate Metabolic Process, Protein targeting to Nucleus, Autophagy, Cancer Immune Checkpoints
Protocol
1.Prepare all reagents, samples and standards.
2.Add 100μL standard or sample to each well. Incubate 1 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.
For Research Use Only | Not For Clinical Use
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