DOCK6 ELISA Kit
Quick Overview for DOCK6 ELISA Kit (ABIN6211959)
Target
See all DOCK6 productsReactivity
Detection Method
Method Type
Detection Range
Application
Sample Type
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Minimum Detection Limit
- 0.312 ng/mL
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Purpose
- Human Dedicator Of Cytokinesis Protein 6 (DOCK6) ELISA Kit
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Analytical Method
- Quantitative
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Sensitivity
- < 0.1 ng/mL
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Components
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The kit components listed are for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
- Pre-coated 96-Well Microplate
- Standard
- Standard Diluent Buffer
- Wash Buffer
- Detection Reagent A
- Detection Reagent B
- Diluent A
- Diluent B
- TMB Substrate
- Stop Solution
- Plate Sealer
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Material not included
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- 37 °C incubator
- Multi and single channel pipettes and sterile pipette tips
- Squirt bottle or automated microplate washer
- 1.5 mL tubes
- Distilled water
- Absorbent filter papers
- 100 mL and 1 liter graduated cylinders
- Microplate reader (wavelength: 450 nm)
- ELISA Shaker
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Application Notes
- Optimal dilutions/concentrations should be determined by the end user.
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Comment
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The stability of the kit is determined by the rate of activity loss. The loss rate is less than 5 % within the expiration date under appropriate storage conditions. To minimize performance fluctuations, operation procedures and lab conditions should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same user throughout.
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Plate
- Pre-coated
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Reagent Preparation
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This procedure is provided for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
- 1) Standard: Prepare the standard with the recommended volume of Standard Diluent Buffer, to make the standard solution. Then use the Standard Diluent buffer to carry out serial dilutions of the standard solution, as instructed in the Protocol.
- 2) Wash Buffer: Dilute the concentrated Wash Buffer with distilled water, as instructed in the Protocol.
- 3) Detection Reagent Preparation: Calculate the total volume of working solution required. Dilute Detection Reagent A and Detection Reagent B with Diluent A and Diluent B, respectively, at 1:100.
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Sample Collection
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- Tissue homogenates: The preparation of tissue homogenates will vary depending upon tissue type - this is just an example. Rinse tissues with ice-cold PBS to remove the excess of blood. Weigh before homogenization. Finely mince tissues and homogenize with a tissue homogenizer on ice in PBS and sonicate the cell suspension. Centrifuge the homogenates at 5000 x g for 5 min and collect the supernatant. Assay immediately or aliquot and store at -20 °C.
- Cell lysates: Collect cells into a centrifuge tube and wash with PBS. Centrifuge the cell lysate at 1000 x g for 10 min and discard the supernatant. Add 300-500 μL PBS or NaCl per 1 x 106 cells on ice and sonicate the cell suspension. Centrifuge at 10000 x g for 10 min at 4 °C, collect the supernatant and assay immediately.
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Restrictions
- For Research Use only
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Storage
- 4 °C
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Storage Comment
- Shipped at 4 °C. Upon receipt, store the kit according to the storage instruction in the kit's manual.
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Expiry Date
- 6 months
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- DOCK6 (Dedicator of Cytokinesis 6 (DOCK6))
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Alternative Name
- Dedicator Of Cytokinesis Protein 6
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Background
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Ensembl: ENSG00000130158
UniProt Entry Name: DOCK6_HUMAN
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Gene ID
- 57572
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HGNC
- 19189
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OMIM
- 614194
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UniProt
- Q96HP0
Target See all DOCK6 products
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