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Human COL7 ELISA Kit
Human COL7 ELISA Kit
Catalog # MSPP-SEC147HU
CAS Number:  
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Human COL7 ELISA Kit
Catalog # MSPP-SEC147HU
Supplier Number:  SEC147HU
CAS Number:  

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:
    COL7
  • Size:
    1 kit
  • Sample Type:
    Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
  • Cross Reactivity:
    No significant cross-reactivity or interference between Collagen Type VII (COL7) and analogues was observed
  • Detection Method:
    Colorimetric
  • Time to Results:
    3 h
  • Shelf Life:
    12 Months
  • Detection Range:
    3.12 - 200 ng/ml
  • Storage Temperature:
    4 °C for one month (frequent use), −20 °C for one year
  • Sample Volume:
    100 µl
  • Sensitivity:
    1.33 ng/ml
  • Regulatory Status:
    RUO
  • Cat. No.:
    MSPP-SEC147HU
  • No. of tests:
    96 wells

Specifications

About this item

This assay has high sensitivity and excellent specificity for detecting Human COL7 (Collagen Type VII). The assay range is from 3.12 to 200 ng/ml (Sandwich kit) with a sensitivity of 1.33 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%

Collagen, type VII, alpha 1 encodes the alpha chain of type VII collagen. The type VII collagen fibril, composed of three identical alpha collagen chains, is restricted to the basement zone beneath stratified squamous epithelia. It functions as an anchoring fibril between the external epithelia and the underlying stroma. Mutations in this gene are associated with all forms of dystrophic epidermolysis bullosa. In the absence of mutations, however, an autoimmune response against type VII collagen can result in an acquired form of this disease called epidermolysis bullosa acquisita.Type VII collagen is also found in the retina; its function in this organ is unknown.COL7A1 is located on the short arm of human chromosome 3, in the chromosomal region denoted 3p21.31.

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