STJ13100093

antibody from St John's Laboratory

Targeting: CAMP CAP18, FALL-39, FALL39, LL37

Western blot

Immunocytochemistry

Flow cytometry

Antibody data

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Validation data

Product number: STJ13100093 - Provider product page
Provider: St John's Laboratory
Product name: Anti-CAMP antibody (STJ13100093)
Antibody type: Monoclonal
Description: Mouse monoclonal antibody anti-Cathelicidin is suitable for use in Immunohistochemistry, Immunofluorescence, Western Blot and Flow Cytometry research applications.
Reactivity: Human
Host: Mouse
Conjugate: Unconjugated
Antigen sequence: NA
Epitope: NA
Antibody clone number: NA
Vial size: NA
Concentration: NA
Storage: Maintain the lyophilised/reconstituted antibodies frozen at-20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting, glycerol (1:1) may be added for an additional stability. Avoid freeze and thaw cycles.
Handling: NA

CAMP protein structure - STJ13100093 shown in red.

Supportive validation

Submitted by: St John's Laboratory (provider)
Main image
Experimental details: IF on ethanol-fixed human spermatosoid using Mouse monoclonal to Cathelicidin: OSX12 clone (STJ13100093) at a concentration of 10 ug/ml. DAPI counterstained appearing in blue.
Sample type: NA
Validation comment: NA
Primary Ab dilution: NA
Other comments: NA
Secondary Ab: NA
Secondary Ab dilution: NA
Protocol: NA
Appendix: NA

Supportive validation

Submitted by: St John's Laboratory (provider)
Main image
Experimental details: IF on ethanol-fixed human spermatosoid using Mouse monoclonal to Cathelicidin: OSX12 clone (STJ13100093) at a concentration of 10 ug/ml. DAPI counterstained appearing in blue.
Sample type: NA
Validation comment: NA
Primary Ab dilution: NA
Other comments: NA
Secondary Ab: NA
Secondary Ab dilution: NA
Protocol: NA
Appendix: NA

Supportive validation

Submitted by: St John's Laboratory (provider)
Main image
Experimental details: IF on ethanol-fixed human spermatosoid using Mouse monoclonal to Cathelicidin: OSX12 clone (STJ13100093) at a concentration of 10 ug/ml. DAPI counterstained appearing in blue.
Sample type: NA
Validation comment: NA
Primary Ab dilution: NA
Other comments: NA
Secondary Ab: NA
Secondary Ab dilution: NA
Protocol: NA
Appendix: NA

Supportive validation

Submitted by: St John's Laboratory (provider)
Main image
Experimental details: IF on ethanol-fixed human spermatosoid using Mouse monoclonal to Cathelicidin: OSX12 clone (STJ13100093) at a concentration of 10 ug/ml. DAPI counterstained appearing in blue.
Sample type: NA
Validation comment: NA
Primary Ab dilution: NA
Other comments: NA
Secondary Ab: NA
Secondary Ab dilution: NA
Protocol: NA
Appendix: NA

Supportive validation

Submitted by: St John's Laboratory (provider)
Main image
Experimental details: IF on ethanol-fixed human spermatosoid using Mouse monoclonal to Cathelicidin: OSX12 clone (STJ13100093) at a concentration of 10 ug/ml. DAPI counterstained appearing in blue.
Sample type: NA
Validation comment: NA
Primary Ab dilution: NA
Other comments: NA
Secondary Ab: NA
Secondary Ab dilution: NA
Protocol: NA
Appendix: NA

Supportive validation

Submitted by: St John's Laboratory (provider)
Main image
Experimental details: Staining of a cytospin preparation of peripheral blood mononuclear cells (PBMC) isolated from buffycoat. Cells were left to air dry and then fixed with cold acetone (90 seconds) and blocked with PBS containing 1% FCS and 0. 1% saponin (blocking buffer) for 20 minutes. Cells were then washed twice in PBS and incubated with Mouse monoclonal to Cathelicidin: OSX12 clone (STJ13100093) at a concentration of 10 ug/ml. DAPI counterstained appearing in blue. The antibody selectively recognizes polymorphonuclar cells.
Sample type: NA
Validation comment: NA
Primary Ab dilution: NA
Other comments: NA
Secondary Ab: NA
Secondary Ab dilution: NA
Protocol: NA
Appendix: NA

Supportive validation

Submitted by: St John's Laboratory (provider)
Main image
Experimental details: Staining of a cytospin preparation of peripheral blood mononuclear cells (PBMC) isolated from buffycoat. Cells were left to air dry and then fixed with cold acetone (90 seconds) and blocked with PBS containing 1% FCS and 0. 1% saponin (blocking buffer) for 20 minutes. Cells were then washed twice in PBS and incubated with Mouse monoclonal to Cathelicidin: OSX12 clone (STJ13100093) at a concentration of 10 ug/ml. The antibody selectively recognizes polymorphonuclar cells.
Sample type: NA
Validation comment: NA
Primary Ab dilution: NA
Other comments: NA
Secondary Ab: NA
Secondary Ab dilution: NA
Protocol: NA
Appendix: NA

Supportive validation

Submitted by: St John's Laboratory (provider)
Main image
Experimental details: Staining of a cytospin preparation of peripheral blood mononuclear cells (PBMC) isolated from buffycoat. Cells were left to air dry and then fixed with cold acetone (90 seconds) and blocked with PBS containing 1% FCS and 0. 1% saponin (blocking buffer) for 20 minutes. Cells were then washed twice in PBS and incubated with Mouse monoclonal to Cathelicidin: OSX12 clone (STJ13100093) at a concentration of 10 ug/ml. DAPI counterstained appearing in blue. The antibody selectively recognizes polymorphonuclar cells.
Sample type: NA
Validation comment: NA
Primary Ab dilution: NA
Other comments: NA
Secondary Ab: NA
Secondary Ab dilution: NA
Protocol: NA
Appendix: NA