Human ULBP2 ELISA Kit
- SKU:
- HUFI01846
- Product Type:
- ELISA Kit
- Size:
- 96 Assays
- Uniprot:
- Q9BZM5
- Sensitivity:
- 7.5IU/ml
- Range:
- 12.5-800IU/ml
- ELISA Type:
- Sandwich
- Synonyms:
- ULBP2, ALCAN-alpha, N2DL2, NKG2DL2, RAET1H, ALCAN-alpha, N2DL2, N2DL-2, NKG2D ligand 2, RAET1HNKG2DL2, retinoic acid early transcript 1 H, Retinoic acid early transcript 1H, UL16 binding protein 2, UL16-binding protein 2
- Reactivity:
- Human
- Research Area:
- Immunology
Frequently bought together:
Description
Human ULBP2 ELISA Kit
The Human ULBP2 (UL16-binding protein 2) ELISA Kit is a reliable and accurate tool for measuring ULBP2 levels in human samples. ULBP2 is a stress-induced ligand for the activating immune receptor NKG2D, which plays a critical role in immune surveillance and responses against infected or transformed cells.This kit offers high sensitivity and specificity, allowing for precise quantification of ULBP2 levels in serum, plasma, and cell culture supernatants. Its robust performance ensures consistent and reproducible results, making it an ideal choice for a wide range of research applications related to immune responses and cancer biology.
By measuring ULBP2 levels, researchers can gain valuable insights into immune activation, tumor evasion mechanisms, and potential therapeutic targets for cancer immunotherapy. With its user-friendly protocol and reliable performance, the Human ULBP2 ELISA Kit is a valuable tool for advancing research in immunology and cancer biology.
| Product Name: | Human ULBP2 ELISA Kit |
| Product Code: | HUFI01846 |
| Size: | 96 Assays |
| Alias: | ULBP2, ALCAN-alpha, N2DL2, NKG2DL2, RAET1H, ALCAN-alpha, N2DL2, N2DL-2, NKG2D ligand 2, RAET1HNKG2DL2, retinoic acid early transcript 1 H, Retinoic acid early transcript 1H, UL16 binding protein 2, UL16-binding protein 2 |
| Detection method: | Sandwich ELISA, Double Antibody |
| Application: | This immunoassay kit allows for the in vitro quantitative determination of Human ULBP2 concentrations in serum plasma and other biological fluids. |
| Sensitivity: | 7.5IU/ml |
| Range: | 12.5-800IU/ml |
| Storage: | 4°C for 6 months |
| Note: | For Research Use Only |
| Recovery: | Matrices listed below were spiked with certain level of Human ULBP2 and the recovery rates were calculated by comparing the measured value to the expected amount of Human ULBP2 in samples. | ||||||||||||||||
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| Linearity: | The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Human ULBP2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected. | ||||||||||||||||
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| CV(%): | Intra-Assay: CV<8% Inter-Assay: CV<10% |
| Component | Quantity | Storage |
| ELISA Microplate (Dismountable) | 8×12 strips | 4°C for 6 months |
| Lyophilized Standard | 2 | 4°C/-20°C |
| Sample/Standard Dilution Buffer | 20ml | 4°C |
| Biotin-labeled Antibody(Concentrated) | 120ul | 4°C (Protect from light) |
| Antibody Dilution Buffer | 10ml | 4°C |
| HRP-Streptavidin Conjugate(SABC) | 120ul | 4°C (Protect from light) |
| SABC Dilution Buffer | 10ml | 4°C |
| TMB Substrate | 10ml | 4°C (Protect from light) |
| Stop Solution | 10ml | 4°C |
| Wash Buffer(25X) | 30ml | 4°C |
| Plate Sealer | 5 | - |
Other materials and equipment required:
- Microplate reader with 450 nm wavelength filter
- Multichannel Pipette, Pipette, microcentrifuge tubes and disposable pipette tips
- Incubator
- Deionized or distilled water
- Absorbent paper
- Buffer resevoir
| Uniprot | Q9BZM5 |
| UniProt Protein Function: | ULBP2: Ligand for the NKG2D receptor, together with at least ULBP1 and ULBP3. ULBPs activate multiple signaling pathways in primary NK cells, resulting in the production of cytokines and chemokines. Binding of ULBPs ligands to NKG2D induces calcium mobilization and activation of the JAK2, STAT5, ERK and PI3K kinase/Akt signal transduction pathway. In CMV infected cells, interacts with soluble CMV glycoprotein UL16. The interaction with UL16 blocked the interaction with the NKG2D receptor, providing a mechanism by which CMV infected cells might escape the immune system. UL16 also causes ULBP2 to be retained in the ER and cis- Golgi apparatus so that it does not reach the cell surface. Belongs to the MHC class I family. |
| UniProt Protein Details: | Protein type:Membrane protein, GPI anchor Chromosomal Location of Human Ortholog: 6q25 Cellular Component: anchored to plasma membrane; cell surface; extracellular space Molecular Function:antigen binding; natural killer cell lectin-like receptor binding Biological Process: antigen processing and presentation; natural killer cell activation; natural killer cell mediated cytotoxicity |
| NCBI Summary: | This gene encodes a major histocompatibility complex (MHC) class I-related molecule that binds to the NKG2D receptor on natural killer (NK) cells to trigger release of multiple cytokines and chemokines that in turn contribute to the recruitment and activation of NK cells. The encoded protein undergoes further processing to generate the mature protein that is either anchored to membrane via a glycosylphosphatidylinositol moiety, or secreted. Many malignant cells secrete the encoded protein to evade immunosurveillance by NK cells. This gene is located in a cluster of multiple MHC class I-related genes on chromosome 6. [provided by RefSeq, Jul 2015] |
| UniProt Code: | Q9BZM5 |
| NCBI GenInfo Identifier: | 47605923 |
| NCBI Gene ID: | 80328 |
| NCBI Accession: | Q9BZM5.1 |
| UniProt Secondary Accession: | Q9BZM5,Q5VUN4, |
| UniProt Related Accession: | Q9BZM5 |
| Molecular Weight: | 27,368 Da |
| NCBI Full Name: | NKG2D ligand 2 |
| NCBI Synonym Full Names: | UL16 binding protein 2 |
| NCBI Official Symbol: | ULBP2  |
| NCBI Official Synonym Symbols: | N2DL2; RAET1H; NKG2DL2; ALCAN-alpha  |
| NCBI Protein Information: | NKG2D ligand 2 |
| UniProt Protein Name: | NKG2D ligand 2 |
| UniProt Synonym Protein Names: | ALCAN-alpha; Retinoic acid early transcript 1H; UL16-binding protein 2 |
| Protein Family: | NKG2D ligand |
| UniProt Gene Name: | ULBP2  |
| UniProt Entry Name: | N2DL2_HUMAN |
*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.
Before adding to wells, equilibrate the SABC working solution and TMB substrate for at least 30 min at 37°C. When diluting samples and reagents, they must be mixed completely and evenly. It is recommended to plot a standard curve for each test.
| Step | Protocol |
| 1. | Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells! |
| 2. | Aliquot 0.1ml standard solutions into the standard wells. |
| 3. | Add 0.1 ml of Sample / Standard dilution buffer into the control (zero) well. |
| 4. | Add 0.1 ml of properly diluted sample ( Human serum, plasma, tissue homogenates and other biological fluids.) into test sample wells. |
| 5. | Seal the plate with a cover and incubate at 37 °C for 90 min. |
| 6. | Remove the cover and discard the plate content, clap the plate on the absorbent filter papers or other absorbent material. Do NOT let the wells completely dry at any time. Wash plate X2. |
| 7. | Add 0.1 ml of Biotin- detection antibody working solution into the above wells (standard, test sample & zero wells). Add the solution at the bottom of each well without touching the side wall. |
| 8. | Seal the plate with a cover and incubate at 37°C for 60 min. |
| 9. | Remove the cover, and wash plate 3 times with Wash buffer. Let wash buffer rest in wells for 1 min between each wash. |
| 10. | Add 0.1 ml of SABC working solution into each well, cover the plate and incubate at 37°C for 30 min. |
| 11. | Remove the cover and wash plate 5 times with Wash buffer, and each time let the wash buffer stay in the wells for 1-2 min. |
| 12. | Add 90 µl of TMB substrate into each well, cover the plate and incubate at 37°C in dark within 10-20 min. (Note: This incubation time is for reference use only, the optimal time should be determined by end user.) And the shades of blue can be seen in the first 3-4 wells (with most concentrated standard solutions), the other wells show no obvious color. |
| 13. | Add 50 µl of Stop solution into each well and mix thoroughly. The color changes into yellow immediately. |
| 14. | Read the O.D. absorbance at 450 nm in a microplate reader immediately after adding the stop solution. |
When carrying out an ELISA assay it is important to prepare your samples in order to achieve the best possible results. Below we have a list of procedures for the preparation of samples for different sample types.
| Sample Type | Protocol |
| Serum | If using serum separator tubes, allow samples to clot for 30 minutes at room temperature. Centrifuge for 10 minutes at 1,000x g. Collect the serum fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. If serum separator tubes are not being used, allow samples to clot overnight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Remove serum and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. |
| Plasma | Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples at 4°C for 15 mins at 1000 × g within 30 mins of collection. Collect the plasma fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. Note: Over haemolysed samples are not suitable for use with this kit. |
| Urine & Cerebrospinal Fluid | Collect the urine (mid-stream) in a sterile container, centrifuge for 20 mins at 2000-3000 rpm. Remove supernatant and assay immediately. If any precipitation is detected, repeat the centrifugation step. A similar protocol can be used for cerebrospinal fluid. |
| Cell culture supernatant | Collect the cell culture media by pipette, followed by centrifugation at 4°C for 20 mins at 1500 rpm. Collect the clear supernatant and assay immediately. |
| Cell lysates | Solubilize cells in lysis buffer and allow to sit on ice for 30 minutes. Centrifuge tubes at 14,000 x g for 5 minutes to remove insoluble material. Aliquot the supernatant into a new tube and discard the remaining whole cell extract. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C. |
| Tissue homogenates | The preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenize in 20ml of 1X PBS (including protease inhibitors) and store overnight at ≤ -20°C. Two freeze-thaw cycles are required to break the cell membranes. To further disrupt the cell membranes you can sonicate the samples. Centrifuge homogenates for 5 mins at 5000xg. Remove the supernatant and assay immediately or aliquot and store at -20°C or -80°C. |
| Tissue lysates | Rinse tissue with PBS, cut into 1-2 mm pieces, and homogenize with a tissue homogenizer in PBS. Add an equal volume of RIPA buffer containing protease inhibitors and lyse tissues at room temperature for 30 minutes with gentle agitation. Centrifuge to remove debris. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C. |
| Breast Milk | Collect milk samples and centrifuge at 10,000 x g for 60 min at 4°C. Aliquot the supernatant and assay. For long term use, store samples at -80°C. Minimize freeze/thaw cycles. |
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