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Human ATP7b ELISA Kit
Human ATP7b ELISA Kit
Catalog # MSPP-SEG386HU
CAS Number:  
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Human ATP7b ELISA Kit
Catalog # MSPP-SEG386HU
Supplier Number:  SEG386HU
CAS Number:  
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Specifications

  • Assay duration:
    Multiple steps
  • Assay Type (ELISA with LOV):
    Sandwich
  • Conjugate ELISA:
    Biotin
  • Format:
    Pre-coated
  • Host:
    Rabbit
  • Primary antibody reactivity:
    Human
  • Target protein:
    ATP7b
  • Size:
    1 kit
  • Sample Type:
    Tissue homogenates, cell lysates and other biological fluids
  • Cross Reactivity:
    No significant cross-reactivity or interference between ATPase, Cu++ Transporting Beta Polypeptide (ATP7b) and analogues was observed
  • Detection Method:
    Colorimetric
  • Time to Results:
    3 h
  • Shelf Life:
    12 Months
  • Detection Range:
    0.156 - 10 ng/ml
  • Storage Temperature:
    4 °C for one month (frequent use), −20 °C for one year
  • Sample Volume:
    100 µl
  • Sensitivity:
    0.059 ng/ml
  • Regulatory Status:
    RUO
  • Cat. No.:
    MSPP-SEG386HU
  • No. of tests:
    96 wells

Specifications

About this item

This assay has high sensitivity and excellent specificity for detecting Human ATP7b (ATPase, Cu++ Transporting Beta Polypeptide). The assay range is from 0.156 to 10 ng/ml (Sandwich kit) with a sensitivity of 0.059 ng/ml. There is no detectable cross-reactivity with other relevant proteins. Activity loss rate and accelerated stability test ect have been conducted to guarantee the best performance of the products after long storage and delivery.

  • High sensitivity and specificity
  • Perfect reproducibility and consistency across batches
  • Quality control with three-level inspections
  • Wide range of targets/species available
  • Intra-assay: CV<10%; Inter-assay: CV<12%

ATP7b is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least two putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson's disease.ATP7B gene was 78% in the transduction region, 89% in the channel/phosphorylation regions, and 79% in the ATP-binding region. The predicted length of the gene product was 1,411 amino acids for ATP7B compared with 1500 amino acids for MNK.

Caution: For research use only. Not for use in clinical diagnostic procedures. Please proper stored each component based on the instruction.