Mouse Monoclonal Cytokeratin 1 antibody. Suitable for Flow Cyt, WB, IHC-P, ICC/IF, IHC-Fr and reacts with Human, Mouse, Rat samples. Cited in 40 publications. Immunogen corresponding to Native Full Length Protein corresponding to Human KRT1.
pH: 7.3
Preservative: 0.07% Sodium azide
Constituents: 1% Fetal calf serum
Flow Cyt | WB | IHC-P | ICC/IF | IHC-Fr | |
---|---|---|---|---|---|
Human | Tested | Tested | Expected | Tested | Expected |
Mouse | Predicted | Predicted | Expected | Predicted | Expected |
Rat | Predicted | Predicted | Expected | Predicted | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/20 | Notes ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes For paraffin embedded tissue a TUF pretreatment is recommended. |
Species Rat | Dilution info - | Notes For paraffin embedded tissue a TUF pretreatment is recommended. |
Species Human | Dilution info - | Notes For paraffin embedded tissue a TUF pretreatment is recommended. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes Stains all types of keratin containing cells (epithelia) in frozen sections of various tissues, with the exception of myoepithelial cells. |
Species Rat | Dilution info - | Notes Stains all types of keratin containing cells (epithelia) in frozen sections of various tissues, with the exception of myoepithelial cells. |
Species Human | Dilution info - | Notes Stains all types of keratin containing cells (epithelia) in frozen sections of various tissues, with the exception of myoepithelial cells. |
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May regulate the activity of kinases such as PKC and SRC via binding to integrin beta-1 (ITB1) and the receptor of activated protein C kinase 1 (RACK1). In complex with C1QBP is a high affinity receptor for kininogen-1/HMWK.
KRT16, Keratin, type I cytoskeletal 19, KRT6C, KRT15, KRT18, Keratin, type II cytoskeletal 5, KRT6B, Keratin, type I cytoskeletal 14, KRT4, KRT12, Keratin, type I cytoskeletal 13, Keratin, type I cytoskeletal 9, KRT20, KRT3, KRT2, KRT8, KRT17, KRT6A, KRT7, KRT10
KRTA, KRT1, 67 kDa cytokeratin, Cytokeratin-1, Hair alpha protein, Keratin-1, Type-II keratin Kb1, CK-1, K1
Mouse Monoclonal Cytokeratin 1 antibody. Suitable for Flow Cyt, WB, IHC-P, ICC/IF, IHC-Fr and reacts with Human, Mouse, Rat samples. Cited in 40 publications. Immunogen corresponding to Native Full Length Protein corresponding to Human KRT1.
pH: 7.3
Preservative: 0.07% Sodium azide
Constituents: 1% Fetal calf serum
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Pan Keratin also known as pan-keratin is a complex mixture of intermediate filament proteins essential for the mechanical stability of epithelial cells. These keratins have a range of molecular weights between 40 and 67 kDa. Keratin expression occurs in epithelial tissues where they form a dense network providing structural support. Researchers commonly employ anti-keratin antibodies and anti-pan keratin antibodies to study various epithelial tissues as these antibodies broadly recognize keratin proteins allowing for a comprehensive pan keratin stain in histological applications.
Keratins contribute to cellular integrity and resilience against mechanical stress. They function within the cytoskeleton by forming filamentous networks that link to desmosomes. These filaments involve several keratin types and non-keratin proteins as part of a larger complex. Pan keratin immunostain techniques help visualize these structures demonstrating their important role in maintaining epithelial barrier function and tissue architecture which includes stratified and simple epithelia. The interaction of keratins with other cytoskeletal elements underlines their significance in cellular biology.
Keratins are integral to the cytoskeleton organization and cell adhesion pathways. Cell junctions such as desmosomes rely on keratin filaments for stability and signal transduction. Connections exist with proteins such as desmoplakin and plakoglobin which are important in maintaining cell-cell adhesion and communication. Researchers often use keratin stains to examine epithelial tissue organization giving insights into disruptions within these pathways that can affect tissue function.
Keratin expression patterns serve as markers in diagnosing epithelial-derived tumors such as carcinomas and certain skin disorders. Abnormal keratin expression can indicate epithelial tissue transformation contributing to cancer development or progression. For example variations in specific keratin types are markers for different carcinoma types. Moreover disorders involving the skin like epidermolysis bullosa simplex may relate to mutations in keratin genes. Understanding these connections enables researchers to explore potential therapeutic approaches by targeting related proteins and pathways.
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ICC/IF image of ab8068 stained HeLa cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab8068, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
Overlay histogram showing A431 cells stained with ab8068 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Triton for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab8068, 1/20 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (Goat Anti-Mouse IgG H&L (DyLight® 488) preadsorbed ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1](Mouse IgG1, Kappa Monoclonal [B11/6] - Isotype Control ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
ab8068 staining pan Keratin in Human glioblastoma cell line by ICC/IF (Immunocytochemistry/Immunofluorescence). The cells were fixed with paraformaldehyde; permeabilized with 0.1% Triton X 100 in PBS and blocked with 0.5% BSA for 30 minutes at room temperature. Samples were incubated with primary antibody (1/50 dilution in 0.5% BSA in PBS) for 16hours at 4°C. An Alexa Fluor® 488 anti-mouse was used as a secondary antibody at 1/400 dilution.
All lanes: Western blot - Anti-pan Keratin antibody [80] (ab8068) at 1/250 dilution
All lanes: A431 (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg
All lanes: Western blot - Goat Anti-Mouse IgG H&L (HRP) preadsorbed (Goat Anti-Mouse IgG H&L (HRP) preadsorbed ab97040) at 1/5000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 65 kDa
Observed band size: 49 kDa, 58 kDa, 65 kDa
Exposure time: 30s
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