Menu

Human Ubiquitin Conjugating Enzyme E2I (UBE2I) ELISA Kit

Information

Catalog number

SEE600Hu-10x96

Full name

Human Ubiquitin Conjugating Enzyme E2I (UBE2I) ELISA Kit

Size

10 plates of 96 wells

Price

4782.00 €

Go to shop   

Details

Description

Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Human Ubiquitin Conjugating Enzyme E2I (UBE2I) in samples from Tissue homogenates, cell lysates and other biological fluids with no significant corss-reactivity with analogues from other species. This is a cost efficient bulk pack of 10 plates of 96 wells each, conveniently packed along with the other reagents in 10 separate kits to avoid unsealing the plates and reagents that won't be immediately used.

Specifications

Detection range: 0.156-10ng/mL; Sensitivity: < 0.058ng/mL; Species reactivity: Homo sapiens (Human)

Additional_information

Known also as Ubiquitin Conjugating Enzyme E2I elisa. Alternative names of the recognized antigen: P18; UBC9; UBCE9; SUMO-protein ligase; Ubiquitin carrier protein 9; Ubiquitin carrier protein I; Ubiquitin-protein ligase I; SUMO-conjugating enzyme UBC9

Storage_and_shipping

Transported on ice packs/blue ice. Keep refrigerated at 2-8 degrees Celsius. Shelf life: 6 months.

Notes

Research Use Only.

Properties

E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.

Test

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED

Additional description

Enzymes are cleaving the substrate. If the substrate is DNA they are called restriction enzymes. Activating enzymes will cut off the domain that is biological active to become functional.