You are viewing an incomplete version of our website. Please click to reload the website as full version.

Rat (Rattus) SERPING1 ELISA Kit

Recommended SERPING1 Product (supplied by: Log in to see )

Serpin Peptidase Inhibitor, Clade G (C1 Inhibitor), Member 1 (SERPING1) ELISA Kits
  • C1-INH
  • C1IN
  • C1INH
  • C1nh
  • C1NH
  • fb64f02
  • HAE1
  • HAE2
  • im:7159527
  • LOC100136072
  • si:dkeyp-110g5.2
  • wu:fb60c09
  • wu:fb62a08
  • wu:fb64f02
Rat (Rattus)
Kits with alternative reactivity to:
Methode Type
Competition ELISA
Detection Range
6.17-500 ng/mL
Minimum Detection Limit
6.17 ng/mL
Log in to see
Supplier Product No.
Log in to see

Showcase your results, aid the scientific community, and receive a full refund.

Contribute a validation

Learn more

Available images

Catalog No. ABIN416491
$ 720.00
Plus shipping costs $45.00
Relevance Score ABIN Method Type Sample Type Detection Range Detection Minimum Supplier References Details
0.29927906 ABIN1114301 Sandwich ELISA Serum, Plasma, Biological Fluids 7.81-500 ng/mL 7.81 ng/mL Log in to see
0.29927906 ABIN1568694 Competition ELISA Serum, Plasma, Tissue Homogenate, Cell Lysate, Cell Culture Supernatant, Biological Fluids 6.17-500 ng/mL 6.17 ng/mL Log in to see
0.0012348129 ABIN822550 Sandwich ELISA Serum, Plasma, Cell Culture Supernatant, Bronchoalveolar Lavage, Urine, Tissue Homogenate 15.6-1000 ng/mL 15.6 ng/mL Log in to see
0.0012348129 ABIN626808 Sandwich ELISA Serum, Cell Culture Supernatant, Tissue Homogenate, Plasma, Body Fluids 25-500 ng/mL 25 ng/mL Log in to see
0.0012348129 ABIN2543230 Competition ELISA Serum, Plasma, Biological Fluids 6.17-500 ng/mL 6.17 ng/mL Log in to see
0.0012348129 ABIN1148261 Log in to see
0.0012348129 ABIN2076518 Sandwich ELISA Log in to see
0.0012348129 ABIN2946549 7.813-500 ng/mL 7.813 ng/mL Log in to see


Application / Reactivity Rat (Rattus)


Antigen Serpin Peptidase Inhibitor, Clade G (C1 Inhibitor), Member 1 (SERPING1) ELISA Kits
Reactivity Rat (Rattus)
Kits with alternative reactivity to:
(15), (11), (8), (4), (3), (3), (2), (2), (2), (1), (1), (1)
Methode Type Competition ELISA
Detection Range 6.17-500 ng/mL
Minimum Detection Limit 6.17 ng/mL
Application ELISA
Supplier Log in to see

Product Details SERPING1 ELISA Kit

Target details Application Details Handling Images
Purpose The kit is a competitive inhibition enzyme immunoassay technique for the in vitro quantitative measurement of C1INH in Serum,Plasma,Biological Fluids
Sample Type Serum, Plasma, Biological Fluids
Detection Method Colorimetric
Specificity This assay has high sensitivity and excellent specificity for detection of Complement 1 Inhibitor (C1INH).
Cross-Reactivity (Details) No significant cross-reactivity or interference between Complement 1 Inhibitor (C1INH) and analogues was observed.
Sensitivity 2.26 ng/mL
The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined the mean O.D. Value of 20 replicates of the zero standard added by their three standard deviations.
  • Pre-coated, ready to use 96-well strip plate - 1
  • Plate sealer for 96 wells - 4
  • Standard (liquid) - 2
  • Standard Diluent - 1×20mL
  • Detection Reagent A (green) - 1×120µL
  • Assay Diluent A (2 × concentrate) - 1×6mL
  • TMB Substrate - 1×9mL
  • Stop Solution - 1×6mL
  • Wash Buffer (30 × concentrate) - 1×20mL
  • Instruction manual - 1
Material not included
  • Microplate reader with 450nm 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

Target details

Product Details SERPING1 ELISA Kit Application Details Handling Images back to top
Alternative Name C1INH (SERPING1 ELISA Kit Abstract)
Pathways Complement System

Application Details

Product Details SERPING1 ELISA Kit Target details Handling Images back to top
Application Notes
  • 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.

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.

Sample Volume 50 μL
Assay Time 2.5 h
Plate Pre-coated,Strips (12 x 8)
Protocol This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific for rat C1INH has been pre-coated onto a microplate. A competitive inhibition reaction is launched between Horseradish Peroxidase (HRP) labeled rat C1INH and unlabeled rat C1INH (Standards or samples) with the pre-coated antibody specific for rat C1INH. After incubation the unbound conjugate is washed off. The amount of bound HRP conjugate is reverse proportional to the concentration of C1INH in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of C1INH in the sample.
  • Prepare all reagents, samples and standards,
  • Add 50 µL standard or sample to each well. And then add 50 µL prepared Detection Reagent A immediately. Incubate 1 hour at 37 °C,
  • Aspirate and wash 5 times,
  • Add 90 µL Substrate Solution. Incubate 15-25 minutes at 37 °C,
  • Add 50 µL Stop Solution. Read at 450 nm immediately.
Reagent Preparation
  • Bring all kit components and samples to room temperature (18-25°C) before use.
  • Standard - Reconstitute the Standard with 0.4mL of Standard Diluent, kept for 10 minutes at room temperature, shake gently (not to foam). The concentration of the standard in the stock solution is 500ng/mL. Please prepare 5 tubes containing 0.6mL Standard Diluent and produce a triple dilution series. Mix each tube thoroughly before the next transfer. Set up 5 points of diluted standard such as 500ng/mL, 166.7ng/mL, 55.6ng/mL, 18.5ng/mL, 6.17ng/mL, and the last EP tubes with Standard Diluent is the blank as 0ng/mL.
  • Assay Diluent A - Dilute 6mL of Assay Diluent A Concentrate (2×) with 6mL of deionized or distilled water to prepare 12 mL of Assay Diluent A. The prepared working dilution cannot be frozen.
  • Detection Reagent A - Briefly spin or centrifuge the stock Detection A before use. Dilute to the working concentration with working Assay Diluent A (1:100).
  • Wash Solution - Dilute 20mL of Wash Solution concentrate (30×) with 580mL of deionized or distilled water to prepare 600 mL of Wash Solution (1×).
  • TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.
  • Making serial dilution in the wells directly is not permitted.
  • Prepare standard within 15 minutes before assay. Please do not dissolve the reagents at 37°C directly.
  • Please carefully reconstitute Standards or working Detection Reagent A according to the instruction, and avoid foaming and mix gently until the crystals have completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10µL for once pipetting.
  • The reconstituted Standards and Detection Reagent A can be used only once.
  • If crystals have formed in the Wash Solution concentrate (30×), warm to room temperature and mix gently until the crystals have completely dissolved.
  • Distilled water is recommended to be used to make the preparation for reagents or samples. Contaminated water or container for reagent preparation will influence the detection result.
Sample Collection Serum: Allow samples to clot for two hours at room temperature or overnight at 4°C before centrifugation for 20 minutes at approximately 1000 × g. Assay immediately or store samples in aliquot at -20°C or -80°C. Avoid repeated freeze/thaw cycles.

Plasma: Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 15 minutes at 1000 × g within 30 minutes of collection. Remove plasma and assay immediately or store samples in aliquot at -20°C or -80°C. Avoid repeated freeze/thaw cycles.

Biological Fluids: Centrifuge samples for 20 minutes at 1000 × g. Remove particulates and assay immediately or store samples in aliquot at -20 °C or -80 °C for later use. Avoid repeated freeze/thaw cycles.
Sample Preparation Notes:
  • The supplier is only responsible for the kit itself, but not for the samples consumed during the assay. The user should calculate the possible amount of the samples used in the whole test. Please reserve sufficient samples in advance.
  • Please predict the concentration before assaying. If values for these are not within the range of the standard curve, users must determine the optimal sample dilutions for their particular experiments.
  • Serum/plasma samples require about a 5,000 fold dilution. For example, to prepare a 1:5,000 dilution of sample, transfer 10µL of sample to 490µL PBS. This yields a 1:50 dilution. Next, dilute the 1:50 sample by transferring 10µL to 990µL PBS. You now have a 1:5,000 dilution of your sample. Mix thoroughly at each stage. Sample should be diluted by 0.02mol/L PBS(PH=7.0-7.2).
  • If the samples are not indicated in the manual, a preliminary experiment to determine the validity of the kit is necessary.
  • Tissue or cell extraction samples prepared by chemical lysis buffer may cause unexpected ELISA results due to the impacts of certain chemicals.
  • Owing to the possibility of mismatching between antigen from other resource and antibody used in our kits (e.g., antibody targets conformational epitope rather than linear epitope), some native or recombinant proteins from other manufacturers may not be recognized by our products.
  • Influenced by the factors including cell viability, cell number and also sampling time, samples from cell culture supernatant may not be detected by the kit.
  • Fresh samples without long time storage is recommended for the test. Otherwise, protein degradation and denaturalization may occur in those samples and finally lead to wrong results.
Assay Procedure
  • 1. Determine wells for diluted standard, blank and sample. Prepare 5 wells for standard, 1 well for blank. Add 50 µL each of dilutions of standard (read Reagent Preparation ), blank and samples into the appropriate wells, respectively. And then add 50 µL of Detection Reagent A to each tube immediately. Shake the plate gently. Cover with a Plate sealer. Incubate for 1 hour at 37 °C. Detection Reagent A may appear cloudy. Warm to room temperature and mix gently until solution appears uniform.
  • 2. Aspirate the solution and wash with 350 µL of 1X Wash Solution to each well using a squirt bottle, multi-channel pipette, manifold dispenser or autowasher, and let it sit for 1-2 minutes. Remove the remaining liquid from all wells completely by snapping the plate onto absorbent paper. Repeat 5 times. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against absorbent paper.
  • 3. Add 90 µL of Substrate Solution to each well. Cover with a new Plate sealer. Incubate for 15 - 25 minutes at 37 °C (Don't exceed 30 minutes). Protect from light. The liquid will turn blue by the addition of Substrate Solution.
  • 4. Add 50 µL of Stop Solution to each well. The liquid will turn yellow by the addition of Stop solution. Mix the liquid by tapping the side of the plate. If color change does not appear uniform, gently tap the plate to ensure thorough mixing.
  • 5. Remove any drop of water and fingerprint on the bottom of the plate and confirm there is no bubble on the surface of the liquid. Then, run the microplate reader and conduct measurement at 450 nm immediately.
  • 1. Assay preparation: Keep appropriate numbers of strips for 1 experiment and remove extra strips from microtiter plate. Removed strips should be resealed and stored at -20 °C until the kits expiry date.
  • 2. Samples or reagents addition: Please use the freshly prepared Standard. Please carefully add samples to wells and mix gently to avoid foaming. Do not touch the well wall as possible. For each step in the procedure, total dispensing time for addition of reagents or samples to the assay plate should not exceed 10 minutes. This will ensure equal elapsed time for each pipetting step, without interruption. To avoid cross-contamination, change pipette tips between additions of each standard level, between sample additions, and between reagent additions. Also, use separate reservoirs for each reagent.
  • 3. Incubation: To ensure accurate results, proper adhesion of plate sealers during incubation steps is necessary. Do not allow wells to sit uncovered for extended periods between incubation steps. Once reagents have been added to the well strips, DO NOT let the strips DRY at any time during the assay. Incubation time and temperature must be observed.
  • 4. Washing: The wash procedure is critical. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Solution by aspirating or decanting and remove any drop of water and fingerprint on the bottom of the plate. Insufficient washing will result in poor precision and falsely elevated absorbance reading.
  • 5. Controlling of reaction time: Observe the change of color after adding TMB Substrate (e.g. observation once every 10 minutes), if the color is too deep, add Stop Solution in advance to avoid excessively strong reaction which will result in inaccurate absorbance reading.
  • 6. TMB Substrate is easily contaminated. Please protect it from light.
Calculation of Results This assay employs the competitive inhibition enzyme immunoassay technique, so there is an inverse correlation between C1INH concentration in the sample and the assay signal intensity. Low levels of C1INH result in a high O.D value, while a high concentration of C1INH results in a low signal. Average the duplicate readings for each standard, control, and samples. Create a standard curve on log-log graph paper, with C1INH concentration on the y-axis and absorbance on the x-axis. Draw the best fit straight line through the standard points and it can be determined by regression analysis. Using some plot software, such as curve expert 1.30, is also recommended. If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor.
In order to make the calculation easier, we plot the O.D. value of the standard (X-axis) against the log of concentration of the standard (Y-axis), although concentration is indeed the independent variable while O.D. value is the dependent variable. The O.D. values of the standard curve may vary according to the conditions of assay performance (e.g. operator, pipetting technique, washing technique or temperature effects). This curve is provided for demonstration only. The customers should establish their own standard curve for each test conducted.
Assay Precision Intra-assay Precision (precision within an assay): Three samples with low, medium and high levels of the target antigen were tested twenty times on one plate, respectively.
Inter-assay Precision (precision between assays): Three samples with low, medium and high levels of the target antigen were tested on three different plates, eight replicates in each plate.
CV (%) = SD/mean X 100
  • Intra-assay: CV less than 10 %
  • Inter-assay: CV less than 12 %
Restrictions For Research Use only


Product Details SERPING1 ELISA Kit Target details Application Details Images back to top
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 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.
Storage 4 °C/-20 °C
Storage Comment
  • 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 0 °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 30 °C can be considered as 2 months at 0 °C, which means 3 days at 30 °C equaling 6 months at 0 °C.
Expiry Date 6 months


Product Details SERPING1 ELISA Kit Target details Application Details Handling back to top
Supplier Images
ELISA image for SERPING1 ELISA Kit (Serpin Peptidase Inhibitor, Clade G (C1 Inhibitor), Member 1) (ABIN416491) Serpin Peptidase Inhibitor, Clade G (C1 Inhibitor), Member 1 (SERPING1) ELISA Kit