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Mouse Rps14 / 40S ribosomal protein S14 ELISA Kit

SKU:
MOFI00590
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P62264
Sensitivity:
46.875pg/ml
Range:
78.125-5000pg/ml
ELISA Type:
Sandwich
Synonyms:
Rps14, 40S ribosomal protein S14
Reactivity:
Mouse
€649
Frequently bought together:

Description

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Mouse Rps14/ 40S ribosomal protein S14 ELISA Kit

The Mouse RPS14 (40S Ribosomal Protein S14) ELISA Kit is a highly precise and reliable assay designed for the accurate measurement of RPS14 levels in mouse serum, plasma, and cell lysates. This kit boasts high sensitivity and specificity, ensuring consistent and reproducible results for a variety of research applications.RPS14 is a vital component of the 40S ribosomal subunit and plays a crucial role in protein synthesis. Dysregulation of RPS14 has been linked to various diseases, including cancer, developmental disorders, and autoimmune conditions.

As such, this ELISA kit serves as a valuable tool for studying the role of RPS14 in these diseases and potential therapeutic interventions.Overall, the Mouse RPS14 (40S Ribosomal Protein S14) ELISA Kit is a must-have for researchers looking to deepen their understanding of ribosomal protein biology and its implications in disease pathology.

Product Name:Mouse Rps14 / 40S ribosomal protein S14 ELISA Kit
Product Code:MOFI00590
Size:96 Assays
Alias:Rps14, 40S ribosomal protein S14
Detection Method:Sandwich ELISA
Application:This immunoassay kit allows for the in vitro quantitative determination of Mouse Rps14 concentrations in serum plasma and other biological fluids.
Sensitivity:46.875pg/ml
Range:78.125-5000pg/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery: Matrices listed below were spiked with certain level of Mouse Rps14 and the recovery rates were calculated by comparing the measured value to the expected amount of Mouse Rps14 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)86-10292
EDTA plasma(n=5)88-10598
UFH plasma(n=5)86-10396
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mouse Rps14 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)87-96%85-95%90-104%
EDTA plasma(n=5)84-101%83-100%84-97%
UFH plasma(n=5)87-98%83-97%83-88%
Intra Assay:CV <8%
Inter Assay:CV <10%
ComponentQuantityStorage
ELISA Microplate (Dismountable)8-12 strips4°C for 6 months
Lyophilized Standard24°C/-20°C
Sample/Standard Dilution Buffer20ml4°C
Biotin-labeled Antibody(Concentrated)120ul4°C (Protect from light)
Antibody Dilution Buffer10ml4°C
HRP-Streptavidin Conjugate(SABC)120ul4°C (Protect from light)
SABC Dilution Buffer10ml4°C
TMB Substrate10ml4°C (Protect from light)
Stop Solution10ml4°C
Wash Buffer(25X)30ml4°C
Plate Sealer5-

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
UniprotP62264
UniProt Protein Function:RPS14: a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S11P family of ribosomal proteins. It is located in the cytoplasm. Transcript variants utilizing alternative transcription initiation sites have been described in the literature. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. In Chinese hamster ovary cells, mutations in this gene can lead to resistance to emetine, a protein synthesis inhibitor. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
UniProt Protein Details:

Protein type:RNA-binding; Ribosomal; Translation

Chromosomal Location of Human Ortholog: 18 E1|18 34.4 cM

Cellular Component: extracellular matrix; focal adhesion; membrane; mitochondrion; nucleolus

Molecular Function:mRNA 5'-UTR binding; RNA binding; structural constituent of ribosome; translation regulator activity

Biological Process: erythrocyte differentiation; maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA); negative regulation of transcription from RNA polymerase II promoter; ribosomal small subunit assembly and maintenance; translation

UniProt Code:P62264
NCBI GenInfo Identifier:31981100
NCBI Gene ID:20044
NCBI Accession:NP_065625.2
UniProt Secondary Accession:P62264,P06366, Q544W4,
UniProt Related Accession:P62264
Molecular Weight:16,273 Da
NCBI Full Name:40S ribosomal protein S14
NCBI Synonym Full Names:ribosomal protein S14
NCBI Official Symbol:Rps14  
NCBI Official Synonym Symbols:AL023078; 2600014J02Rik  
NCBI Protein Information:40S ribosomal protein S14
UniProt Protein Name:40S ribosomal protein S14
Protein Family:40S ribosomal protein
UniProt Gene Name:Rps14  

*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.

StepProcedure
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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