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Rat SP-1 ELISA Kit (RTFI00412)

SKU:
RTFI00412
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
Q01714
Sensitivity:
46.875pg/ml
Range:
78.125-5000pg/ml
ELISA Type:
Sandwich
Synonyms:
SP1, Sp1 transcription factor, Transcription factor Sp1, TSFP1
Reactivity:
Rat
Research Area:
Cell Biology
€649

Description

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Rat SP-1 ELISA Kit

The Rat SP-1 ELISA Kit is a powerful tool for researchers looking to accurately measure SP-1 levels in rat serum, plasma, and cell culture supernatants. With its high sensitivity and specificity, this kit delivers dependable and consistent results, making it suitable for a variety of research applications.SP-1, also known as Specificity Protein 1, is a key transcription factor that plays a crucial role in regulating gene expression and cell growth. Its dysregulation has been implicated in various diseases, including cancer, diabetes, and cardiovascular disorders, making it a valuable biomarker for studying these conditions and developing potential therapeutic interventions.

By utilizing the Rat SP-1 ELISA Kit, researchers can gain valuable insights into the role of SP-1 in disease pathology and progression, ultimately leading to a better understanding of these conditions and the development of novel treatment strategies.

Product Name:Rat Sp1 (Transcription factor Sp1) ELISA Kit
Product Code:RTFI00412
Size:96 Assays
Target:Rat Sp1
Alias:SP1, Sp1 transcription factor, Transcription factor Sp1, TSFP1
Reactivity:Rat
Detection Method:Sandwich ELISA, Double Antibody
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 Rat Sp1 and the recovery rates were calculated by comparing the measured value to the expected amount of Rat Sp1 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)89-10295
EDTA plasma(n=5)90-10596
UFH plasma(n=5)86-10391
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat Sp1 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)86-105%85-94%89-102%
EDTA plasma(n=5)87-100%90-95%92-97%
UFH plasma(n=5)87-100%80-95%82-93%
Intra-Assay:CV <8%
Inter-Assay:CV <10%
Uniprot:Q01714
UniProt Protein Function:SP1: a transcription factor of the Sp1 C2H2-type zinc-finger protein family. Phosphorylated and activated by MAPK. Dephosphorylation by PTEN inhibits DNA binding. Binds to p38 in the nucleus. Interacts with Huntingtin and TAFII130. Transcriptional activity of SP1 and TAFII130 disrupted in early Huntingtin's Disease.
UniProt Protein Details:

Protein type:DNA-binding; Transcription factor; C2H2-type zinc finger protein

Cellular Component: nucleoplasm; cytoplasm; nuclear chromatin; nucleus

Molecular Function:protein C-terminus binding; histone acetyltransferase binding; protein binding; protein homodimerization activity; DNA binding; sequence-specific DNA binding; histone deacetylase binding; metal ion binding; double-stranded DNA binding; bHLH transcription factor binding; transcription factor activity; transcription factor binding

Biological Process: transcription from RNA polymerase II promoter; embryonic placenta development; ossification; in utero embryonic development; megakaryocyte differentiation; embryonic skeletal development; positive regulation of transcription, DNA-dependent; embryonic process involved in female pregnancy; rhythmic process; enucleate erythrocyte differentiation; liver development; trophectodermal cell differentiation; regulation of transcription from RNA polymerase II promoter; regulation of transcription, DNA-dependent; positive regulation of transcription from RNA polymerase II promoter; embryonic camera-type eye morphogenesis; lung development

NCBI Summary:transcription factor that recognizes 5'-CCGCCC promoter sequence; plays a role in transcriptional regulation of many genes [RGD, Feb 2006]
UniProt Code:Q01714
NCBI GenInfo Identifier:164414419
NCBI Gene ID:24790
NCBI Accession:NP_036787.2
UniProt Secondary Accession:Q01714,Q8K4R0,
UniProt Related Accession:Q01714
Molecular Weight:80,772 Da
NCBI Full Name:transcription factor Sp1
NCBI Synonym Full Names:Sp1 transcription factor
NCBI Official Symbol:Sp1  
NCBI Protein Information:transcription factor Sp1; trans-acting transcription factor 1
UniProt Protein Name:Transcription factor Sp1
Protein Family:Sex-specific storage-protein
UniProt Gene Name:Sp1  
UniProt Entry Name:SP1_RAT
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 clotovernight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Removeserum 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 anti-coagulant. 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 & homogenizein 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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