Mouse monoclonal antibody against Cytokeratin (pan) (Clone ISM005)
Mouse monoclonal antibody against Cytokeratin (pan) (Clone ISM005)
Product identification
ISC048-R03 3 ml ready-to-use (RTU)
ISC048-R07 7 ml ready-to-use (RTU)
ISC048-C02 0.2 ml concentrated
ISC048-C05 0.5 ml concentrated
Summary and explanation
Broad-spectrum Cytokeratin CK (Pan) mainly marks keratinized epithelium, stratified squamous epithelium, stratified epithelium, proliferative keratinocytes and simple epithelium, and can be used for squamous cell carcinoma (including splindle variant), various adenocarcinomas (including adrenal carcinoma, hepatocellular carcinoma), transitional cell carcinoma, small cell carcinoma, malignant mesothelioma, germ cell tumors (except seminoma), some synovial sarcomas, and leiomyosarcomas. In differential diagnosis, it can be combined with EMA and CEA and other indicators to perform differential diagnosis between epithelial tumors and non-epithelial tumors, and can also be used for the study of various cancers
Principle of the procedure
The stated primary antibody is suitable for immunohistochemical staining of FFPE tissue sections based on specific antigen-antibody reaction. Using a detection system linked to HRP or alkaline phosphatase the antigen visualization is performed via specific binding of the primary antibody. Secondary antibody is binding to the primary antibody, and the enzyme complex labels this complex. The enzymatic activation of the chromogen results in a visible reaction product at the antigen site. Each step is incubated for a precise time and temperature and requires interposed washing steps. The specimen may then be counterstained. Results are interpreted using a light microscope.
Staining procedure
- Cut 3-4 μm section of formalin-fixed paraffin-embedded tissue and place on positively charged slides.
- Dry at 65°C for 2 hours.
- Deparaffinize, rehydrate, and epitope retrieve. Upon completion, rinse with 3 changes of distilled or deionized water.
- If using HRP detection system, place slides in peroxide block for 10 minutes; rinse. If using AP detection system, omit this step.
- Apply the antibody and incubate for 60 minutes; rinse.
- Apply the InSituVison™ Polymer Rabbit/Mouse Detection System for 30 minutes; rinse.
- Apply ample amount of DAB or AEC chromogen and incubate; rinse.
- Dehydrate and coverslip.
Interpretation of results
The immunostaining procedure causes a colored reaction product to precipitate at the antigen sites localized by the primary antibody.
Cellular localization: Cytoplasm.
A qualified pathologist experienced in immunohistochemistry procedures must evaluate positive and negative tissue controls before interpreting patient specimens.
Positive staining intensity should be assessed within the context of any background staining of the negative reagent control.
Note: A negative result means that the antigen in question was not detected, but not that the antigen is not present in the cells/tissues tested. An antibody panel may be used to support the results in some circumstances. Additionally, the morphology of each tissue sample should be examined utilizing a hematoxylin and eosin stained section. A qualified pathologist must interpret the patient’s morphologic findings and pertinent clinical data.
Warnings and precautions
- Application only by qualified and trained personnel.
- There are no estimated health risks, if the product is used as directed. MSDS is available on request.
- Product contains sodium azide as preservative. Pure sodium azide is toxic. The concentration of sodium azide in this reagent is < 0.1 % and is not classified hazardous.
See MSDS.
- As with any product derived from biological sources, proper handling procedures should be used.
- Do not use reagents after expiration date.
- Take reasonable precautions when handling reagents. Use protective clothing and gloves.
- All hazardous materials should be disposed according to guidelines for hazardous waste disposal. Materials of human or animal origin should be handled as biohazardous materials and disposed of with proper precautions.
- Avoid microbial contamination of reagents as it may cause incorrect results.
Materials provided
| Primary antibody | Cytokeratin pan |
| Host | Mouse |
| Subclass | IgG |
| Clone | ISM005 |
| Species Cross-reactivity | Human. Others-not known |
| Applications | Immunohistochemistry |
| Epitope Retrieval | Heat-induced epitope retrieval |
| Ready-to-use antibody | Prediluted antibody in antibody diluent buffer |
Product label shows the specific lot number.
Prediluted antibody is ready-to-use and optimized for staining. No further dilution, reconstitution, mixing, or titration is needed.
Materials required but not provided
The following materials may be required for staining but are not provided with the primary antibody.
– Positive and negative controls
– Microscope slides (positively charged) and cover slips
– Water bath
– Humidified chamber
– Staining jars
– Stopwatch
– Xylene or xylene substitute
– Ethanol
– Deionized or distilled water
– Antigen retrieval reagent, e.g. Antigen Enhancer (HIER buffer), Cat. No. BUAN01-500
– Detection system, e.g. IHC Complete Detection system (Goat anti mouse/rabbit HRP, DAB staining), Cat. No. D001-15
– Wash buffer: e.g. IHC Wash Buffer, Cat. No. BUWA01-1000
– Tap water/bluing reagent (e.g. ammonia water)
– Light microscope
Storage and handling
Store at 2 – 8 °C.
When stored correctly antibody is stable to the expiration date indicated on the vial. Do not use after expiration date.
To ensure proper reagent delivery and stability of the antibody, replace the dispenser cap after every use and immediately place the bottle cool in an upright position.
Literature
[1] Owens, MA, Horten, BC, Da Silva MM. HER2 amplification ratios by fluorescence in situ hybridization and correlation with immunohistochemistry in a cohort of 6556 breast cancer tissues. Clinical breast cancer, 2004,5(1), 63-69.
[2] Gibbons-Fideler IS, Nitta H, Murillo A, et al. Identification of her2 immunohistochemistry-negative, fish-amplified breast cancers and their response to anti-her2 neoadjuvant chemotherapy. Am J Clin Pathol, 2019, 151(2):176-184.
Date of publication or revision
2024-06-10
Change(s) made
Explanation of symbols
