Latin name
Capra aegagrus hircus
Notes
For research use only.
Properties
E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays
Additional description
The kilo Daltons subunit weight of Goat protein A 70 DNA binding subunit(RPA1) ELISA kit compared to your protein ladder can be shifted a little due to electrophoresis effects. 1 kDa = 1000 g/mol protein
Storage_and_shipping
Storage: store at 2-8°C Stability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
Specifications
Recognized antigen: Replication protein A 70 kDa DNA binding subunit(RPA1); Species reactivity: Goat; Sensitivity: 0.1ng/mL; Detection range: 2.5-50ng/mL; Principle: competitive ELISA; Reproducibility: Intra-Assay: CV
Description
A competitive ELISA for quantitative measurement of Goat Replication protein A 70 kDa DNA binding subunit(RPA1) in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Additional_information
Kit contents: 1. MICROTITER PLATE * 1 2. ENZYME CONJUGATE*1 vial 3. STANDARD A*1 vial 4. STANDARD B*1 vial 5. STANDARD C*1 vial 6. STANDARD D*1 vial 7. STANDARD E*1 vial 8. STANDARD F*1 vial 9. SUBSTRATE A*1 vial 10. SUBSTRATE B*1 vial 11. STOP SOLUTION*1 vial 12. WASH SOLUTION (100 x)*1 vial 13. BALANCE SOLUTION*1 vial 14. INSTRUCTION*1
Test
ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED,Replication factor subunits and DNA replication proteins are found in DNA replication complexes like GINS, MCM,.. and replication initiators producing two identical replicas of DNA from one original DNA molecule. This process occurs in all living organisms and is the basis for biological inheritance. DNA is made up of a double helix of two strands, and each strand of the original DNA molecule gene serves as a template for the production of the complementary strand, a process referred to as semiconservative replication. Cellular proofreading and error-checking mechanisms ensure near perfect fidelity for DNA replication of genes.