Precision
NA
Assay Type
NA
Stability
NA
Test Principle
NA
Cross Activity
NA
Specificity
NA
Species Reactivity
Rat
Shipping Conditions
Ice packs
Assay Time
1-5 hours
Sensitivity
0.078 ng/mL
Detection Method
Colorimetric
Latin name
Rattus norvegicus
Estimated Turnaround Time
6-11 business days
Detection Range
0.312 ng/mL-20 ng/mL
Research Area
Epigenetics and Nuclear Signaling
Storage Temperature
Short term: 4°C; Long term: see manual.
Sample Type
serum, plasma, tissue homogenates, cell lysates
Target Name
replication protein A 70 kDa DNA-binding subunit
Application
For research use only. Not for diagnostic procedures.
Quality Systems
The kit is manufactured at ISO 9001 certified facilities.
Precaution of Use
The Stop Solution is acidic. Do not allow to contact skin or eyes.
Target's alterntive name
HSSB, MST075, REPA1, RF-A, RP-A, RPA70, MSTP075|replication protein A1
Shelf life
Use Rat replication protein A 70 kDa DNA-binding subunit (RPA1) ELISA kit before 6 months
Properties
E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays
Description
The kilo Daltons subunit weight of 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
About
Rats are used to make rat monoclonal anti mouse antibodies. There are less rat- than mouse clones however. Rats genes from rodents of the genus Rattus norvegicus are often studied in vivo as a model of human genes in Sprague-Dawley or Wistar rats.
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.
