The largest database of trusted experimental protocols

Rabbit anti ck19

Manufactured by Abcam
Sourced in United States

Rabbit anti-CK19 is a primary antibody that recognizes the cytokeratin 19 (CK19) protein. CK19 is a member of the keratin family of intermediate filament proteins, which are essential structural components of epithelial cells. This antibody can be used to detect and identify CK19-expressing cells in various research applications.

Automatically generated - may contain errors

6 protocols using rabbit anti ck19

1

Quantification of Pancreatic ADM and AFLs

Check if the same lab product or an alternative is used in the 5 most similar protocols
For quantification of ADM and AFLs, random whole pancreatic sections stained with hematoxylin and eosin H&E were analyzed. For immunohistochemical staining, sections of paraffin embedded pancreata were rehydrated and antigen retrieval was performed using Antigen Unmasking Solution (Vector Laboratories). Overnight incubation with the following primary antibodies was done at 4°C: goat anti-CPA1 (R&D), rabbit anti-CK19 (Abcam), rabbit anti-GFP (Santa Cruz Biotechnology), mouse anti-Ki67 (BD), rabbit anti-P53 (Vector Laboratories), goat anti-Amylase (Santa Cruz Biotechnology), rabbit anti-p44/p42 MAPK (Cell Signaling) and FITC-conjugated DBA-lectin (Vector Laboratories). Biotin-conjugated secondary antibodies were incubated for 1 h at room temperature, following development with ABC and DAB kits (both Vector Laboratories). Nuclear counterstaining was performed using haematoxylin. For immunofluorescence, sections were incubated with fluorophore-conjugated secondary antibody for 1 h at room temperature. Slides were mounted with DAPI hardset antifade mounting medium.
+ Open protocol
+ Expand
2

Immunohistochemical Profiling of Cell Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
Immunohistochemistry was performed as previously described65 (link). The following primary antibodies were used: rabbit anti-Cleaved caspase 3 (1:200; Cell Signalling #9661), mouse anti-CD45 (1:20, BDPharmigen #550539), rabbit anti-CK19 (1:1000; Abcam #ab133496), goat anti-CPA1 (1:300, RD Systems #AF2765), mouse anti–Ki-67 (1:400; BDPharmigen #550609), mouse anti-MUC5AC (1:200; Cell Marque #292M-95), rabbit anti-p65 (C-20) (1:200, Santa Cruz #sc-372), rabbit anti-phospho-STAT3 (Y705) (1:100, Cell Signaling #9145).
+ Open protocol
+ Expand
3

Immunohistochemical Analysis of TLR2 in Liver

Check if the same lab product or an alternative is used in the 5 most similar protocols
The tissues were sliced with the thickness of 5 μm sections with routine deparaffinization. The sections were incubated with rabbit-anti-TLR2 antibody, rabbit-anti-α-SMA, rabbit-anti-CK-19 (Abcam, Cambridge, USA), Goat-anti-rabbit IgG H&L (HRP) (Affinity bioscience, Jiangsu, China) and DAB staining (Solarbio, Beijing, China). Details of the antibodies were presented in Table 1. The expression levels of TLR2 in liver were digitized and analyzed using Image-Pro Plus software.
+ Open protocol
+ Expand
4

Detecting Breast and Epithelial Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
Western blot and Immunofluorescence staining were performed to detect breast and epithelial cell markers. Primary antibodies used were mouse anti-EMA (Dako), rabbit anti-Pan-Ck (Abcam), rabbit anti-Ck19 (Abcam), mouse anti-estrogen receptor (ER) α (Abcam), rabbit anti-ERβ (Abcam) and mouse anti-progesterone receptor (PR) (Abcam). Secondary antibodies used in Western blot analysis were horse-radish peroxidase conjugated goat anti-rabbit and anti-mouse antibodies (Dako). Secondary antibodies used in immunofluorescence study were Alexa Fluor 594 goat anti-rabbit (Life Technologies) and Alexa Fluor 488 goat anti-mouse (Life Technologies). Antibody concentrations used in Western blot and immunofluorescence staining were as recommended by the antibody manufacturers.
+ Open protocol
+ Expand
5

Protein Expression Profiling in ATII Cells after MC-LR Exposure

Check if the same lab product or an alternative is used in the 5 most similar protocols
Proteins were purified from lungs or ATII cells after exposure to MC-LR for 48 h. Western blot analysis of cellular lysates was performed as previously described (Wang et al., 2014 (link)). The following primary antibodies were employed: Rabbit anti-CK18, rabbit anti-CK19, rabbit anti-SP-C, rabbit anti-E-cadherin, rabbit anti-ZO-1, rabbit anti-occludin, rabbit anti-vimentin, rabbit anti-ERK1/2, rabbit anti-p-ERK1/2, rabbit anti-Akt, rabbit anti-p-Akt, mouse anti-MEK1/2, rabbit anti-p-MEK1/2, rabbit anti-PTEN, rabbit anti-GAPDH, mouse anti-MEK1/2 and mouse anti-β-actin (Abcam Inc. Cambridge, MA). Horseradish peroxidase-conjugated goat anti-rabbit/mouse IgG (Boster, Wuhan, China) was used as the secondary antibody. Immunoreactive protein bands were detected using an Odyssey Scanning System (LI-COR Inc).
+ Open protocol
+ Expand
6

Histopathological Analysis of Rat Liver Tissues

Check if the same lab product or an alternative is used in the 5 most similar protocols
Liver tissues were collected immediately at the time rats were sacrificed. Liver samples were fixed by paraformaldehyde and embedded in paraffin. Sections were subjected to hematoxylin and eosin (H&E), immunohistochemistry (IHC), Sirius red staining according to the standard protocols. Antibodies used for IHC staining are as follows: Rabbit anti-Fah (AbboMax, San Jose, CA, 1:3000), Rabbit anti-Ki67 (novocastra, 1:1000), Rabbit anti-α-SMA (Abcam, 1:200), Rabbit anti-Ck19 (Abcam, 1:200).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!