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Bovine Dna Fragmentation Factor Subunit Beta (DFFB) ELISA Kit-Sandwich

Cat. No.EK11F706

Product TypeAnimal Immunoassay Kits

Size

Product Overview

BioVenic Bovine Dna Fragmentation Factor Subunit Beta (DFFB) ELISA Kit-Sandwich is designed for the quantitative determination of Bovine Dna Fragmentation Factor Subunit Beta (DFFB) in serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids using a Sandwich ELISA method. For research use only.

Specifications

Assay Type ELISA-Sandwich
Specificity The assay kit is specific for Bovine DFFB.
Target Species Bovine
Species Reactivity Bovine
Reproducibility Intra-Assay: CV < 10%; Inter-Assay: CV < 10%
Assay Time Around 270 min
Sample Requirement Serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids.

Target Information

DNA Fragmentation Factor Subunit Beta (DFFB), which is also known as Caspase-activated DNase (CAD), is a protein encoded by the DFFB gene in cattle. It is involved in apoptosis (programmed cell death). It breaks down DNA during apoptosis, leading to cell fragmentation. DFFB promotes cell differentiation. DFFB usually exists as an inactive monomer, inhibited by ICAD (inhibitor of caspase-activated DNase).

Target/Biomarker Bovine DFFB
Target Synonym DNA fragmentation factor subunit beta; DNA fragmentation factor, 40 kD, beta polypeptide
Gene ID 535981
UniProt ID Q2KHU4

Shipping and Storage

This product is shipped with gel ice packs. It is recommended to store at 2-8 °C (Up to 6 months).

Documents

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

References

  1. Gutiérrez-Gil, B. et al. An interpretive review of selective sweep studies in Bos taurus cattle populations: identification of unique and shared selection signals across breeds. Frontiers in genetics. 2015, 6.
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