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HOW DID OUR
ANTIBODY PERFORM?
ANTIBODY CUSTOMER REVIEW: Laminin a-1 Polyclonal Antibody (STJ93888)
What was used?
Primary antibody: STJ93888 Laminin a-1
Provider: St John's Laboratory Ltd.
Dilution ratio: 1:50
Application: Immunofluorescence staining
Materials for validation: Decellularised cornea
Click for product data sheet PDF
What Was The Protocol?
Treatment of Materials Tissue was sectioned at a 7 um thickness, and then fixed with 4% parafolmaldehyde and
permeabilized with 1% Triton X-100.
Fixation 4 % parafolmadehyde at room temperature for 20 minutes.
Permeabilization 1% Triton X-100 at room temperature for 5 minutes.
Blocking Blocking buffer (PBS with BSA and goat serum) for 1 hour.
Primary Antibody Probing Primary antibody was added to the solution of blocking buffer (PBS with BSA and goat serum),
at 4˚C overnight.
Sample Wash The sample was washed with PBS with BSA and goat serum 5 times, each for 5 minutes.
Secondary Antibody Probing Secondary antibody was added to the solution of blocking buffer (PBS with BSA and goat serum)
with a 1:100 dilution ratio, for 1 hour.
Sample Wash The sample was washed with PBS with BSA and goat serum 7 times, each for 5 minutes.
Visualization Nikon Axiovert microscope.
What was the protocol?
No. Antigen
Primary
antibody
Primary
antibody
dilution ratio
Secondary
antibody
dilution ratio
1
Decellularised
cornea
STJ93888
Laminin a-1
antibody
1:50 1:00
What were the results?
What did the customer think?
Antibody Specificity:
Antibody RPPA Rating:
Testing results were provided independently by F. Abidin at Newcastle University. They
stated “Visible laminin staining was observed from this tissue section.”
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Immunofluorescence Antibody Customer Review for Laminin α-1 Polyclonal Antibody (STJ93888)

  • 1. HOW DID OUR ANTIBODY PERFORM? ANTIBODY CUSTOMER REVIEW: Laminin a-1 Polyclonal Antibody (STJ93888)
  • 2. What was used? Primary antibody: STJ93888 Laminin a-1 Provider: St John's Laboratory Ltd. Dilution ratio: 1:50 Application: Immunofluorescence staining Materials for validation: Decellularised cornea Click for product data sheet PDF
  • 3. What Was The Protocol? Treatment of Materials Tissue was sectioned at a 7 um thickness, and then fixed with 4% parafolmaldehyde and permeabilized with 1% Triton X-100. Fixation 4 % parafolmadehyde at room temperature for 20 minutes. Permeabilization 1% Triton X-100 at room temperature for 5 minutes. Blocking Blocking buffer (PBS with BSA and goat serum) for 1 hour. Primary Antibody Probing Primary antibody was added to the solution of blocking buffer (PBS with BSA and goat serum), at 4˚C overnight. Sample Wash The sample was washed with PBS with BSA and goat serum 5 times, each for 5 minutes. Secondary Antibody Probing Secondary antibody was added to the solution of blocking buffer (PBS with BSA and goat serum) with a 1:100 dilution ratio, for 1 hour. Sample Wash The sample was washed with PBS with BSA and goat serum 7 times, each for 5 minutes. Visualization Nikon Axiovert microscope.
  • 4. What was the protocol? No. Antigen Primary antibody Primary antibody dilution ratio Secondary antibody dilution ratio 1 Decellularised cornea STJ93888 Laminin a-1 antibody 1:50 1:00
  • 5. What were the results?
  • 6. What did the customer think? Antibody Specificity: Antibody RPPA Rating: Testing results were provided independently by F. Abidin at Newcastle University. They stated “Visible laminin staining was observed from this tissue section.”
  • 7. JOIN THE ANTIBODY VALIDATION PROJECT
  • 8. 1. Order any STJ9 catalogued product using this online form. 2. Test it in your laboratory using your preferred method. 3. Return a fully completed review form to receive rewards. …in 3 simple steps…