Human [Protein ADP-ribosylarginine] hydrolase (ADPRH) ELISA Kit

SKU:BHE13703162
Overview
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Human [Protein ADP-ribosylarginine] hydrolase (ADPRH) ELISA Kit quantifies Human [Protein ADP-ribosylarginine] hydrolase (ADPRH) in serum, plasma, and cell culture supernatants using a sandwich ELISA format. Includes all components for standard-curve based quantification.
Assay Format Sandwich ELISA
Detection Method Colorimetric
Compatible Sample Types Cell Culture Supernatant, Serum, Plasma
Species Reactivity Human
Assay Time Multiple steps standard sandwich ELISA assay with a working time of 3-5 hours. It depends on the experience of the operation person.
Available Options
Size (4) - 48 T, 96 T, 96 T×5, 96 T×50
Options selector
Catalog no. Size
KTE60946-48T 48 T
KTE60946-96T 96 T
KTE60946-96TX5 96 T×5
KTE60946-96TX50 96 T×50
Field Specification
Accession Number {"text":"P54922","url":"http://www.uniprot.org/uniprot/P54922"}
Alternative Names ADPRH; ARH1; ADP-ribose-L-arginine cleaving enzyme
Assay Time
  • Multiple steps standard sandwich ELISA assay with a working time of 3-5 hours. It depends on the experience of the operation person.
Assay Type
  • Sandwich ELISA (quantitative)
Detection Method
  • Colorimetric
Gene ID 141
Product Type
  • Sandwich ELISA Kit
Reactivity
  • Human
Sample Type(s) Cell culture supernatants, Serum, Plasma, Other biological fluids
Shipping Gel pack with blue ice.
Storage The unopened kit should be stored at 2 - 8°C. After opening, please store refer to protocols.

Features & Benefits

Human [Protein ADP-ribosylarginine] hydrolase (ADPRH) ELISA Kit has high sensitivity and excellent specificity for detection of Human ADPRH. No significant cross-reactivity or interference between Human ADPRH and analogues was observed.

Background

The deduced human ADPRH protein has 357 amino acids and an estimated molecular mass of 39.5 kD. Human ADPRH shows 83% amino acid identity to rat Adprh and 82% identity to mouse Adprh. The authors found that the mouse and rat Adprh sequences contain 5 conserved cysteine residues; the human sequence contains only 4 cysteines, with cys108 in rat corresponding to ser103 in human.

Expression of recombinant wildtype and mutant rat and human ADPRH proteins in E. coli and assessment of their DTT requirements for hydrolase activity demonstrated that cys108 is responsible for the DTT dependence of rat Adprh. Northern blot analysis detected a 4.1-kb ADPRH transcript in various human tissues, including fetal and adult brain.

What sample types are compatible with this ELISA kit?

This [Protein ADP-ribosylarginine] hydrolase (ADPRH) ELISA kit is validated for use with Cell culture supernatants, Serum, Plasma, Other biological fluids. Samples should be collected, processed, and stored correctly to preserve analyte integrity — avoid repeated freeze-thaw cycles and centrifuge to remove particulates before use. Dilute samples exceeding the kit's detection range using the supplied assay diluent. Hemolytic, icteric, or lipemic samples may affect assay performance and should be tested with caution.

What is the assay format and detection principle?

This is a sandwich ELISA kit employing an HRP (horseradish peroxidase)-conjugated secondary antibody paired with a TMB (3,3′,5,5′-tetramethylbenzidine) colorimetric substrate. In the sandwich format, the target analyte [Protein ADP-ribosylarginine] hydrolase (ADPRH) captured on the microplate surface is detected by the conjugated antibody, generating a colorimetric signal proportional to analyte concentration. The reaction is stopped and absorbance measured at 450 nm on a standard microplate reader.

How long does the complete assay take?

The complete protocol, from sample addition to final plate reading, requires approximately 3–5 hours. This includes two incubation periods (analyte binding and detection antibody steps), intermediate wash cycles to remove unbound material, 15–30 minutes of TMB substrate development, and final stop-solution addition before absorbance reading. Exact timing will vary with experience level and the number of samples processed in parallel.

What equipment and instruments are required?

Required equipment: (1) a microplate spectrophotometer capable of reading absorbance at 450 nm (reference wavelength 540–570 nm recommended for background correction); (2) precision single-channel or multichannel pipettes; (3) a plate washer or multichannel aspirator; (4) a microcentrifuge for sample clarification; and (5) a 37°C incubator or stable room-temperature environment. No fluorescence or luminescence reader is required — standard colorimetric plate readers are fully compatible with this kit.

Can this kit detect [Protein ADP-ribosylarginine] hydrolase (ADPRH) in species not listed in the specification?

This ELISA kit is formally validated for Human. Cross-reactivity with species not listed in the specification has not been independently characterized. Variability in protein sequence homology across species means that performance in unlisted species cannot be guaranteed without additional validation. For cross-species detection requirements or non-standard sample matrices, please contact BioHippo support or refer to the manufacturer's technical team for guidance.

Can't Find What You're Looking For? We can help you source the best match or customize an ELISA solution for your study. Options may include alternative target synonyms, different species reactivity, sample type/matrix compatibility (serum/plasma/lysate/supernatant), assay format (sandwich/competitive), sensitivity/range, detection chemistry (colorimetric/fluorescent/chemiluminescent), plate format (pre-coated/uncoated, strips vs full plate), and bulk or custom packaging. Click Talk to a Scientist to submit a request form, email us at support@biohippo.com, or explore our Research Services for additional support. Our team will be in contact with you shortly.

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