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Human ART1 (GPI-linked NAD (P) (+) ? ?arginine ADP-ribosyltransferase 1) ELISA Kit (HUFI05481)

SKU:
HUFI05481
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P52961
Sensitivity:
0.094ng/ml
Range:
0.156-10ng/ml
ELISA Type:
Sandwich
Synonyms:
ADP ribosyltransferase 1, ART1, ART2, CD296, Mono(ADP ribosyl)transferase 1, RT6
Reactivity:
Human
€599

Description

Human ART1 (GPI-linked NAD (P) (+)–arginine ADP-ribosyltransferase 1) ELISA Kit (HUFI05481)

The Human ART1 (GPI-linked NAD(P) Arginine ADP-ribosyltransferase 1) ELISA Kit is specifically designed for the precise and accurate detection of ART1 levels in human biological samples such as serum, plasma, and cell culture supernatants. This ELISA kit offers exceptional sensitivity and specificity, guaranteeing dependable and consistent results for a variety of research applications.ART1 is a critical enzyme involved in post-translational modifications, specifically ADP-ribosylation, and is linked to GPI (glycosylphosphatidylinositol). It plays a significant role in various cellular processes, including immune response regulation and cell signaling pathways.

ART1 is also implicated in diseases such as inflammation, autoimmune disorders, and cancer, making it a valuable biomarker for studying these conditions and exploring potential therapeutic interventions.Overall, the Human ART1 ELISA Kit is a valuable tool for researchers seeking to investigate the role of ART1 in physiological and pathological processes, offering precise and reliable quantification of ART1 levels in human samples.

Product Name:Human ART1 (GPI-linked NAD (P) (+) arginine ADP-ribosyltransferase 1) ELISA Kit
Product Code:HUFI05481
Size:96 Assays
Alias:ADP ribosyltransferase 1 ELISA Kit, ART1 ELISA Kit, ART2 ELISA Kit, CD296 ELISA Kit, Mono(ADP ribosyl)transferase 1 ELISA Kit, RT6 ELISA Kit
Detection method:Sandwich ELISA, Double Antibody
Application:This immunoassay kit allows for the in vitro quantitative determination of Human ART1 (GPI-linked NAD (P) (+) arginine ADP-ribosyltransferase 1) 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 ART1 (GPI-linked NAD (P) (+) arginine ADP-ribosyltransferase 1) and the recovery rates were calculated by comparing the measured value to the expected amount of Human ART1 (GPI-linked NAD (P) (+) arginine ADP-ribosyltransferase 1) in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)87-9690
EDTA plasma(n=5)86-9591
heparin plasma(n=5)85-10598
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Human ART1 (GPI-linked NAD (P) (+) arginine ADP-ribosyltransferase 1) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)88-105%85-103%85-104%
EDTA plasma(n=5)83-94%89-95%89-99%
UFH plasma(n=5)88-99%89-96%83-100%
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
UniProt Protein Function:ART1: Has ADP-ribosyltransferase activity toward GLP1R. Belongs to the Arg-specific ADP-ribosyltransferase family.
UniProt Protein Details:Protein type:Transferase; Membrane protein, GPI anchor; EC 2.4.2.31

Chromosomal Location of Human Ortholog: 11p15

Cellular Component: cell surface; integral to plasma membrane; plasma membrane; sarcoplasmic reticulum membrane

Molecular Function:NAD(P)+-protein-arginine ADP-ribosyltransferase activity; NAD+ ADP-ribosyltransferase activity

Biological Process: innate immune response; protein amino acid ADP-ribosylation

NCBI Summary:ADP-ribosyltransferase catalyzes the ADP-ribosylation of arginine residues in proteins. Mono-ADP-ribosylation is a posttranslational modification of proteins that is interfered with by a variety of bacterial toxins including cholera, pertussis, and heat-labile enterotoxins of E. coli. The amino acid sequence consists of predominantly hydrophobic N- and C-terminal regions, which is characteristic of glycosylphosphatidylinositol (GPI)-anchored proteins. This gene was previously designated ART2. [provided by RefSeq, Jul 2008]
UniProt Code:P52961
NCBI GenInfo Identifier:206729882
NCBI Gene ID:417
NCBI Accession:P52961.2
UniProt Secondary Accession:P52961,Q6NTD2, Q96KT9,
UniProt Related Accession:P52961
Molecular Weight:36,335 Da
NCBI Full Name:GPI-linked NAD(P)(+)--arginine ADP-ribosyltransferase 1
NCBI Synonym Full Names:ADP-ribosyltransferase 1
NCBI Official Symbol:ART1
NCBI Official Synonym Symbols:RT6; ART2; ARTC1; CD296
NCBI Protein Information:GPI-linked NAD(P)(+)--arginine ADP-ribosyltransferase 1
UniProt Protein Name:GPI-linked NAD(P)(+)--arginine ADP-ribosyltransferase 1
UniProt Synonym Protein Names:ADP-ribosyltransferase C2 and C3 toxin-like 1; ARTC1; Mono(ADP-ribosyl)transferase 1; CD_antigen: CD296
Protein Family:Arrestin family protein
UniProt Gene Name:ART1
UniProt Entry Name:NAR1_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.
Antibodies
Anti-ART1 Antibody (CAB10103)
ART1 Antibody (PACO07228)
ART1 Antibody (PACO62127)
ART1 Antibody, HRP conjugated (PACO62128)
ART1 Antibody, FITC conjugated (PACO62129)

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