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Rat TNNT1 (Troponin T Type 1, Slow Skeletal) ELISA Kit

SKU:
RTFI00443
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
Q7TNB2
Sensitivity:
9.375pg/ml
Range:
15.625-1000pg/ml
ELISA Type:
Sandwich
Synonyms:
Tnnt1, Troponin T Type 1, Slow Skeletal
Reactivity:
Rat
€649
Frequently bought together:

Description

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Rat TNNT1 (Troponin T Type 1, Slow Skeletal) ELISA Kit

The Rat TNNT1 (Troponin T Type 1 Slow Skeletal) ELISA Kit is a highly reliable and accurate assay for measuring levels of troponin T type 1 slow skeletal in rat serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, delivering consistent and reproducible results for a variety of research applications.Troponin T type 1 slow skeletal is a critical protein involved in muscle contraction and regulation, making it an essential biomarker for studying muscle function and disorders.

Changes in troponin T levels can be indicative of cardiac and skeletal muscle damage, making this kit valuable for monitoring health conditions and assessing treatment efficacy.Whether studying muscle physiology, cardiac health, or muscle-related disorders, the Rat TNNT1 ELISA Kit provides researchers with a reliable tool for quantifying troponin T levels accurately and efficiently. Trust in the precision and quality of this kit for your research needs.

Product Name:Rat Tnnt1 (Troponin T, slow skeletal muscle) ELISA Kit
Product Code:RTFI00443
Size:96 Assays
Target:Rat Tnnt1
Alias:Tnnt1, Troponin T Type 1, Slow Skeletal
Reactivity:Rat
Detection Method:Sandwich ELISA, Double Antibody
Sensitivity:9.375pg/ml
Range:15.625-1000pg/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery:Matrices listed below were spiked with certain level of Rat Tnnt1 and the recovery rates were calculated by comparing the measured value to the expected amount of Rat Tnnt1 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)85-10294
EDTA plasma(n=5)93-10399
UFH plasma(n=5)88-10194
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat Tnnt1 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%87-104%91-101%
EDTA plasma(n=5)82-101%88-100%83-96%
UFH plasma(n=5)81-100%81-98%85-100%
Intra-Assay:CV <8%
Inter-Assay:CV <10%
Uniprot:Q7TNB2
UniProt Protein Function:TNNT1: Troponin T is the tropomyosin-binding subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity. Defects in TNNT1 are the cause of nemaline myopathy type 5 (NEM5); also known as Amish nemaline myopathy (ANM). A form of nemaline myopathy. Nemaline myopathies are muscular disorders characterized by muscle weakness of varying severity and onset, and abnormal thread-or rod-like structures in muscle fibers on histologic examination. Nemaline myopathy type 5 is a severe and progressive form common among Old Order Amish. Affected infants display tremors with hypotonia and mild contractures of the shoulders and hips. Proximal contractures progressively weaken and a pectus carinatum deformity develops before children die of respiratory insufficiency, usually in the second year. Belongs to the troponin T family. 3 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:Contractile; Motility/polarity/chemotaxis

Cellular Component: troponin complex

Molecular Function:tropomyosin binding; troponin T binding

Biological Process: negative regulation of muscle contraction; regulation of muscle contraction; skeletal muscle contraction; slow-twitch skeletal muscle fiber contraction; transition between fast and slow fiber

NCBI Summary:human homolog plays a role in the calcium sensitivity of contraction in skeletal muscle [RGD, Feb 2006]
UniProt Code:Q7TNB2
NCBI GenInfo Identifier:471270250
NCBI Gene ID:171409
NCBI Accession:NP_001264191.1
UniProt Secondary Accession:Q7TNB2,Q7TNA9, Q7TNB0, Q7TNB1, Q923S7,
UniProt Related Accession:Q7TNB2
Molecular Weight:30,010 Da
NCBI Full Name:troponin T, slow skeletal muscle isoform 4
NCBI Synonym Full Names:troponin T type 1 (skeletal, slow)
NCBI Official Symbol:Tnnt1  
NCBI Official Synonym Symbols:sTnT; tnTs; Fang2  
NCBI Protein Information:troponin T, slow skeletal muscle
UniProt Protein Name:Troponin T, slow skeletal muscle
UniProt Synonym Protein Names:Slow skeletal muscle troponin T; sTnT
Protein Family:Troponin
UniProt Gene Name:Tnnt1  
UniProt Entry Name:TNNT1_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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