The largest database of trusted experimental protocols

Ready to use anti er rabbit monoclonal antibody clone sp1

Manufactured by Agilent Technologies
Sourced in United Kingdom, United States

The Ready-to-use anti-ER rabbit monoclonal antibody (clone SP1) is a laboratory reagent designed for the detection of estrogen receptor (ER) proteins in biological samples. This antibody is pre-diluted and ready-to-use, providing a convenient solution for researchers conducting immunohistochemistry or other ER-related studies.

Automatically generated - may contain errors

5 protocols using ready to use anti er rabbit monoclonal antibody clone sp1

1

Immunohistochemical Staining of Tissue

Check if the same lab product or an alternative is used in the 5 most similar protocols
IHC staining of paraffin-embedded tissue sections was carried out using the Envision System (Dako, Glostrup, Denmark) as described previously13 (link). The primary antibodies used were as follows: anti-FSCN1 mouse monoclonal antibody (clone 55k-2, diluted at 1:100, Santa Cruz Biotechnology, Santa Cruz, USA); anti-EGFR rabbit polyclonal antibody (clone 1005, diluted at 1:100, Santa Cruz Biotechnology); HercepTest (Dako); ready-to-use anti-ER rabbit monoclonal antibody (clone SP1, Dako); ready-to-use anti-PR mouse monoclonal antibody (clone PR636, Dako).
+ Open protocol
+ Expand
2

Tissue Array and IHC Analysis in Breast Cancer

Check if the same lab product or an alternative is used in the 5 most similar protocols
Tissue Array Preparation: We followed the methods described by Wang et al.28 (link). In brief, the Quick-Ray® UT-06 (Unitma Co., Ltd., Seoul, Korea) tissue microarray system and the Quick-Ray premade recipient block (UB-06) wax model were used to prepare tissue specimens (1 mm in diameter). Two representative sites from each breast cancer tissue sample were selected for sampling. IHC Analysis: IHC staining of paraffin-embedded tissue sections used the Envision System (Dako, Glostrup, Denmark), as described previously25 (link),26 (link). Primary antibodies consisted of anti-WTAP rabbit monoclonal antibody (clone EPR18744, diluted at 1:3200; Abcam, Cambridge, England), ready-to-use anti-ER rabbit monoclonal antibody (clone SP1, Dako), ready-to-use anti-PR mouse monoclonal antibody (clone PgR636, Dako), ready-to-use anti-Podoplanin mouse monoclonal antibody (clone D2-40, Dako) and HercepTest (Dako). The secondary antibody was Dako’s HRP rabbit/mouse universal antibody (Dako, Glostrup, Denmark). The negative control was incubated with vehicle then with secondary antibody, without primary antibody.
+ Open protocol
+ Expand
3

Immunohistochemical Staining of Paraffin-Embedded Tissues

Check if the same lab product or an alternative is used in the 5 most similar protocols
IHC staining of paraffin-embedded tissue sections used the Envision System (Dako, Glostrup, Denmark), as described previously [5 (link), 30 (link)]. Primary antibodies consisted of anti-METTL14 mouse monoclonal antibody (clone CL4252, diluted at 1 : 1000; Abcam, Cambridge, England), ready-to-use anti-ER rabbit monoclonal antibody (clone SP1, Dako), ready-to-use anti-PR mouse monoclonal antibody (clone PgR636, Dako), HercepTest (Dako), and ready-to-use anti-Ki-67 mouse monoclonal antibody (clone MIB-1, Dako).
+ Open protocol
+ Expand
4

Immunohistochemical Analysis of Breast Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
Immunohistochemical analysis was conducted as described previously.[20 (link)] The primary antibodies used were anti-p-STAT3 mouse monoclonal antibody (clone M9C6; diluted at 1:75; Cell Signaling Technology, Boston, USA), Hercep Test (Dako), ready-to-use anti-ER rabbit monoclonal antibody (clone SP1, Dako), ready-to-use anti-PR mouse monoclonal antibody (clone PgR636, Dako), and ready-to-use anti-Ki-67 mouse monoclonal antibody (clone MIB-1, Dako).
+ Open protocol
+ Expand
5

Immunohistochemical Analysis of Breast Cancer Biomarkers

Check if the same lab product or an alternative is used in the 5 most similar protocols
We followed the methods of Wang et al. [18 (link)]. The primary antibodies consisted of anti-resistin mouse monoclonal antibody (clone C-10, diluted at 1 : 25; Santa Cruz Biotechnology, Santa Cruz, USA), anti-EGFR rabbit polyclonal antibody (clone 1005, diluted at 1 : 100; Santa Cruz Biotechnology), anti-ERK1/2 rabbit monoclonal antibody (clone EPR18444, diluted at 1 : 1000; Abcam, Cambridge, England), ready-to-use anti-ER rabbit monoclonal antibody (clone SP1, Dako), ready-to-use anti-PR mouse monoclonal antibody (clone PgR636, Dako), HercepTest (Dako), and ready-to-use anti-Ki-67 mouse monoclonal antibody (clone MIB-1, Dako).
+ 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!