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Mouse Bone sialoprotein 2 ELISA Kit

SKU:
MOFI00342
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
Q61711
Sensitivity:
0.188ng/ml
Range:
0.313-20ng/ml
ELISA Type:
Sandwich
Synonyms:
Ibsp, BSP, IBSP, BNSP, BSP, BSP-II, SP-II, Integrin-Binding Bone Sialoprotein, Bone Sialoprotein
Reactivity:
Mouse
Research Area:
Signal Transduction
€649
Frequently bought together:

Description

system_update_altDatasheetsystem_update_altMSDS

Mouse Bone sialoprotein 2 ELISA Kit

The Mouse Bone Sialoprotein 2 (BSP2) ELISA Kit is specifically designed for the accurate quantification of BSP2 levels in mouse samples, including serum, plasma, and cell culture supernatants. This kit provides high sensitivity and specificity, ensuring precise and reproducible results for a variety of research applications.BSP2 is a critical protein involved in bone formation and remodeling, playing a key role in skeletal development and maintenance. Dysregulation of BSP2 is associated with various bone diseases, making it a valuable biomarker for studying bone health and potential therapeutic interventions.

With its reliable performance and ease of use, the Mouse BSP2 ELISA Kit is a valuable tool for researchers investigating bone physiology, osteoporosis, and other bone-related disorders. It offers a comprehensive solution for accurate BSP2 measurement, facilitating in-depth studies and advancements in bone research.

Product Name:Mouse Bone sialoprotein 2 ELISA Kit
Product Code:MOFI00342
Size:96 Assays
Alias:Ibsp, BSP, IBSP, BNSP, BSP, BSP-II, SP-II, Integrin-Binding Bone Sialoprotein, Bone Sialoprotein
Detection Method:Sandwich ELISA
Application:This immunoassay kit allows for the in vitro quantitative determination of Mouse Ibsp concentrations in serum plasma and other biological fluids.
Sensitivity:0.188ng/ml
Range:0.313-20ng/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery: Matrices listed below were spiked with certain level of Mouse Ibsp and the recovery rates were calculated by comparing the measured value to the expected amount of Mouse Ibsp in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)91-10499
EDTA plasma(n=5)86-10295
UFH plasma(n=5)88-10499
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mouse Ibsp and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)90-105%85-105%91-105%
EDTA plasma(n=5)82-101%84-92%83-100%
UFH plasma(n=5)86-98%95-98%87-99%
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
UniprotQ61711
UniProt Protein Function:Sialoprotein-2: Binds tightly to hydroxyapatite. Appears to form an integral part of the mineralized matrix. Probably important to cell-matrix interaction. Promotes Arg-Gly-Asp-dependent cell attachment.
UniProt Protein Details:

Protein type:Secreted; Cell adhesion; Secreted, signal peptide; Motility/polarity/chemotaxis

Cellular Component: extracellular space; membrane; extracellular region

Biological Process: osteoblast differentiation; ossification; extracellular matrix organization and biogenesis; biomineral formation; cell adhesion

UniProt Code:Q61711
NCBI GenInfo Identifier:341942035
NCBI Gene ID:15891
NCBI Accession:Q61711.2
UniProt Secondary Accession:Q61711,Q61363, Q80VR6,
UniProt Related Accession:Q61711
Molecular Weight:
NCBI Full Name:Bone sialoprotein 2
NCBI Synonym Full Names:integrin binding sialoprotein
NCBI Official Symbol:Ibsp  
NCBI Official Synonym Symbols:BSP; Bsp2; BSPII; BSP II  
NCBI Protein Information:bone sialoprotein 2; bone sialoprotein II; cell-binding sialoprotein; integrin-binding sialoprotein
UniProt Protein Name:Bone sialoprotein 2
UniProt Synonym Protein Names:Bone sialoprotein II; BSP II; Cell-binding sialoprotein; Integrin-binding sialoprotein
Protein Family:Bone sialoprotein
UniProt Gene Name:Ibsp  
UniProt Entry Name:SIAL_MOUSE

*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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