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Human IFIT1 / Interferon-induced protein with tetratricopeptide repeats 1 ELISA Kit

SKU:
HUFI01406
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P09914
Sensitivity:
0.094ng/ml
Range:
0.156-10ng/ml
ELISA Type:
Sandwich
Synonyms:
IFIT1, Interferon-induced protein with tetRatricopeptide repeats 1, IFIT-1, Interferon-induced 56 kDa protein, IFI-56K, G10P1, IFI56, IFNAI1, ISG56, GARG-16, IFI-56, ISG56, RNM561
Reactivity:
Human
Research Area:
Immunology
€599
Frequently bought together:

Description

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Human IFIT1/Interferon-induced protein with tetratricopeptide repeats 1 ELISA Kit

The Human IFIT1 (Interferon Induced Protein with Tetratricopeptide Repeats 1) ELISA Kit is a powerful tool for detecting and quantifying IFIT1 levels in human serum, plasma, and cell culture supernatants. With its high sensitivity and specificity, this kit delivers reliable and reproducible results, making it perfect for a variety of research applications.IFIT1 is a key protein that is induced by interferons and plays a critical role in the human immune response to viral infections.

By studying the levels of IFIT1 in different samples, researchers can gain valuable insights into the immune system's antiviral mechanisms and develop novel therapeutic strategies for infectious diseases.Whether you are studying host-virus interactions, immune responses, or developing new antiviral treatments, the Human IFIT1 ELISA Kit from Assay Genie provides a comprehensive solution for accurate IFIT1 detection.

Product Name:Human IFIT1 / Interferon-induced protein with tetratricopeptide repeats 1 ELISA Kit
Product Code:HUFI01406
Size:96 Assays
Alias:IFIT1, Interferon-induced protein with tetRatricopeptide repeats 1, IFIT-1, Interferon-induced 56 kDa protein, IFI-56K, G10P1, IFI56, IFNAI1, ISG56, GARG-16, IFI-56, ISG56, RNM561
Detection method:Sandwich ELISA, Double Antibody
Application:This immunoassay kit allows for the in vitro quantitative determination of Human IFIT1 concentrations in serum plasma and other biological fluids.
Sensitivity:0.094ng/ml
Range:0.156-10ng/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery:Matrices listed below were spiked with certain level of Human IFIT1 and the recovery rates were calculated by comparing the measured value to the expected amount of Human IFIT1 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)86-10391
EDTA plasma(n=5)90-10295
UFH plasma(n=5)91-10195
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Human IFIT1 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)87-103%87-105%87-104%
EDTA plasma(n=5)83-100%82-99%83-99%
UFH plasma(n=5)80-90%86-99%84-95%
CV(%):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
UniprotP09914
UniProt Protein Function:IFIT1: IFN-induced antiviral protein which inhibits expression of viral messenger RNAs lacking 2'-O-methylation of the 5' cap. The ribose 2'-O-methylation would provide a molecular signature to distinguish between self and non-self mRNAs by the host during viral infection. Viruses evolved several ways to evade this restriction system such as encoding their own 2'-O-methylase for their mRNAs or by stealing host cap containing the 2'-O- methylation (cap snatching mechanism). Exhibits antiviral activity against several viruses including human papilloma and hepatitis C viruses. Belongs to the IFIT family.
UniProt Protein Details:Chromosomal Location of Human Ortholog: 10q23.31

Cellular Component: cytoplasm; cytosol

Molecular Function:protein binding; RNA binding

Biological Process: cytokine and chemokine mediated signaling pathway; defense response to virus; intracellular transport of viral proteins in host cell; negative regulation of defense response to virus by host; negative regulation of helicase activity; negative regulation of protein binding; negative regulation of viral genome replication; positive regulation of viral genome replication; response to virus

NCBI Summary:This gene encodes a protein containing tetratricopeptide repeats that was originally identified as induced upon treatment with interferon. The encoded protein may inhibit viral replication and translational initiation. This gene is located in a cluster on chromosome 10 with five other closely related genes. There is a pseudogene for this gene on chromosome 13. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Aug 2012]
UniProt Code:P09914
NCBI GenInfo Identifier:400286381
NCBI Gene ID:3434
NCBI Accession:NP_001257857.1
UniProt Secondary Accession:P09914,Q5T7J1, Q96QM5, B3KS50, D3DR31,
UniProt Related Accession:P09914
Molecular Weight:51,713 Da
NCBI Full Name:interferon-induced protein with tetratricopeptide repeats 1 isoform 3
NCBI Synonym Full Names:interferon induced protein with tetratricopeptide repeats 1
NCBI Official Symbol:IFIT1
NCBI Official Synonym Symbols:C56; P56; G10P1; IFI56; ISG56; IFI-56; IFIT-1; IFNAI1; RNM561; IFI-56K
NCBI Protein Information:interferon-induced protein with tetratricopeptide repeats 1
UniProt Protein Name:Interferon-induced protein with tetratricopeptide repeats 1
UniProt Synonym Protein Names:Interferon-induced 56 kDa protein; IFI-56K; P56
Protein Family:Interferon-induced protein with tetratricopeptide repeats
UniProt Gene Name:IFIT1
UniProt Entry Name:IFIT1_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.

StepProtocol
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 TypeProtocol
SerumIf 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.

PlasmaCollect 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 FluidCollect 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 supernatantCollect 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 lysatesSolubilize 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 homogenatesThe 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 lysatesRinse 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 MilkCollect 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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