Human Developmental Biology ELISA Kits
Human DCLK1 (Doublecortin Like Kinase 1) ELISA Kit (HUES01585)
- SKU:
- HUES01585
- Product Type:
- ELISA Kit
- Size:
- 96 Assays
- Uniprot:
- O15075
- Sensitivity:
- 0.09ng/mL
- Range:
- 0.16-10ng/mL
- ELISA Type:
- Sandwich
- Synonyms:
- CL1, CLICK1, DCAMKL1, DCDC3A, DCLK
- Reactivity:
- Human
- Sample Type:
- Serum, plasma and other biological fluids
- Research Area:
- Developmental Biology
Description
Assay type: | Sandwich |
Format: | 96T |
Assay time: | 4.5h |
Reactivity: | Human |
Detection Method: | Colormetric |
Detection Range: | 0.16-10 ng/mL |
Sensitivity: | 0.10 ng/mL |
Sample Volume Required Per Well: | 100µL |
Sample Type: | Serum, plasma and other biological fluids |
Specificity: | This kit recognizes Human DCLK1 in samples. No significant cross-reactivity or interference between Human DCLK1 and analogues was observed. |
This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human DCLK1. Standards or samples are added to the appropriate micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human DCLK1 and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human DCLK1, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by adding Stop Solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human DCLK1. The concentration of Human DCLK1 in samples can be calculated by comparing the OD of the samples to the standard curve.
UniProt Protein Function: | Probable kinase that may be involved in a calcium-signaling pathway controlling neuronal migration in the developing brain. May also participate in functions of the mature nervous system. |
NCBI Summary: | This gene encodes a member of the protein kinase superfamily and the doublecortin family. The protein encoded by this gene contains two N-terminal doublecortin domains, which bind microtubules and regulate microtubule polymerization, a C-terminal serine/threonine protein kinase domain, which shows substantial homology to Ca2+/calmodulin-dependent protein kinase, and a serine/proline-rich domain in between the doublecortin and the protein kinase domains, which mediates multiple protein-protein interactions. The microtubule-polymerizing activity of the encoded protein is independent of its protein kinase activity. The encoded protein is involved in several different cellular processes, including neuronal migration, retrograde transport, neuronal apoptosis and neurogenesis. This gene is up-regulated by brain-derived neurotrophic factor and associated with memory and general cognitive abilities. Multiple transcript variants generated by two alternative promoter usage and alternative splicing have been reported, but the full-length nature and biological validity of some variants have not been defined. These variants encode different isoforms, which are differentially expressed and have different kinase activities. [provided by RefSeq, Sep 2010] |
UniProt Code: | O15075 |
NCBI GenInfo Identifier: | 6225242 |
NCBI Gene ID: | 9201 |
NCBI Accession: | O15075. 2 |
UniProt Secondary Accession: | O15075,Q5VZY8, Q5VZZ0, Q5VZZ1, B7Z3E9, |
UniProt Related Accession: | O15075 |
Molecular Weight: | 47,681 Da |
NCBI Full Name: | Serine/threonine-protein kinase DCLK1 |
NCBI Synonym Full Names: | doublecortin like kinase 1 |
NCBI Official Symbol: | DCLK1 |
NCBI Official Synonym Symbols: | CL1; DCLK; CLICK1; DCDC3A; DCAMKL1 |
NCBI Protein Information: | serine/threonine-protein kinase DCLK1 |
UniProt Protein Name: | Serine/threonine-protein kinase DCLK1 |
UniProt Synonym Protein Names: | Doublecortin domain-containing protein 3A; Doublecortin-like and CAM kinase-like 1; Doublecortin-like kinase 1 |
Protein Family: | Serine/threonine-protein kinase |
UniProt Gene Name: | DCLK1 |
UniProt Entry Name: | DCLK1_HUMAN |
As the OD values of the standard curve may vary according to the conditions of the actual assay performance (e. g. operator, pipetting technique, washing technique or temperature effects), the operator should establish a standard curve for each test. Typical standard curve and data is provided below for reference only.
Concentration (ng/mL) | O.D | Average | Corrected |
10 | 2.42 2.438 | 2.429 | 2.375 |
5 | 1.489 1.549 | 1.519 | 1.465 |
2.5 | 0.902 0.876 | 0.889 | 0.835 |
1.25 | 0.445 0.479 | 0.462 | 0.408 |
0.63 | 0.269 0.249 | 0.259 | 0.205 |
0.32 | 0.158 0.15 | 0.154 | 0.1 |
0.16 | 0.1 0.11 | 0.105 | 0.051 |
0 | 0.045 0.063 | 0.054 | -- |
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Human DCLK1 were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Human DCLK1 were tested on 3 different plates, 20 replicates in each plate.
Intra-assay Precision | Inter-assay Precision | |||||
Sample | 1 | 2 | 3 | 1 | 2 | 3 |
n | 20 | 20 | 20 | 20 | 20 | 20 |
Mean (ng/mL) | 0.55 | 1.17 | 4.32 | 0.54 | 1.17 | 4.45 |
Standard deviation | 0.03 | 0.06 | 0.17 | 0.03 | 0.06 | 0.17 |
C V (%) | 5.45 | 5.13 | 3.94 | 5.56 | 5.13 | 3.82 |
Recovery
The recovery of Human DCLK1 spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.
Sample Type | Range (%) | Average Recovery (%) |
Serum (n=5) | 86-98 | 93 |
EDTA plasma (n=5) | 87-101 | 93 |
Cell culture media (n=5) | 91-103 | 97 |
Linearity
Samples were spiked with high concentrations of Human DCLK1 and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.
Serum (n=5) | EDTA plasma (n=5) | Cell culture media (n=5) | ||
1:2 | Range (%) | 87-100 | 99-113 | 99-116 |
Average (%) | 94 | 106 | 106 | |
1:4 | Range (%) | 91-104 | 86-101 | 86-100 |
Average (%) | 98 | 92 | 91 | |
1:8 | Range (%) | 90-102 | 87-98 | 83-97 |
Average (%) | 95 | 92 | 90 | |
1:16 | Range (%) | 92-108 | 85-95 | 83-93 |
Average (%) | 99 | 90 | 88 |
An unopened kit can be stored at 4°C for 1 month. If the kit is not used within 1 month, store the items separately according to the following conditions once the kit is received.
Item | Specifications | Storage |
Micro ELISA Plate(Dismountable) | 8 wells ×12 strips | -20°C, 6 months |
Reference Standard | 2 vials | |
Concentrated Biotinylated Detection Ab (100×) | 1 vial, 120 µL | |
Concentrated HRP Conjugate (100×) | 1 vial, 120 µL | -20°C(shading light), 6 months |
Reference Standard & Sample Diluent | 1 vial, 20 mL | 4°C, 6 months |
Biotinylated Detection Ab Diluent | 1 vial, 14 mL | |
HRP Conjugate Diluent | 1 vial, 14 mL | |
Concentrated Wash Buffer (25×) | 1 vial, 30 mL | |
Substrate Reagent | 1 vial, 10 mL | 4°C(shading light) |
Stop Solution | 1 vial, 10 mL | 4°C |
Plate Sealer | 5 pieces | |
Product Description | 1 copy | |
Certificate of Analysis | 1 copy |
- Set standard, test sample and control (zero) wells on the pre-coated plate and record theirpositions. It is recommended to measure each standard and sample in duplicate. Note: addall solutions to the bottom of the plate wells while avoiding contact with the well walls. Ensuresolutions do not foam when adding to the wells.
- Aliquot 100 µL of standard solutions into the standard wells.
- Add 100 µL of Sample / Standard dilution buffer into the control (zero) well.
- Add 100 µL of properly diluted sample (serum, plasma, tissue homogenates and otherbiological fluids) into test sample wells.
- Cover the plate with the sealer provided in the kit and incubate for 90 min at 37 °C.
- Aspirate the liquid from each well, do not wash. Immediately add 100 µL of BiotinylatedDetection Ab working solution to each well. Cover the plate with a plate seal and gently mix. Incubate for 1 hour at 37 °C.
- Aspirate or decant the solution from the plate and add 350 µL of wash buffer to each welland incubate for 1-2 minutes at room temperature. Aspirate the solution from each well andclap the plate on absorbent filter paper to dry. Repeat this process 3 times. Note: a microplatewasher can be used in this step and other wash steps.
- Add 100 µL of HRP Conjugate working solution to each well. Cover with a plate seal andincubate for 30 min at 37 °C.
- Aspirate or decant the solution from each well. Repeat the wash process for five times asconducted in step 7.
- Add 90 µL of Substrate Reagent to each well. Cover with a new plate seal and incubate forapproximately 15 min at 37 °C. Protect the plate from light. Note: the reaction time can beshortened or extended according to the actual color change, but not by more than 30min.
- Add 50 µL of Stop Solution to each well. Note: Adding the stop solution should be done inthe same order as the substrate solution.
- Determine the optical density (OD value) of each well immediately with a microplate readerset at 450 nm.