The largest database of trusted experimental protocols

Anti lamin a antibody

Manufactured by Merck Group
Sourced in United States, Japan

The Anti-lamin A antibody is a laboratory reagent used to detect and study the lamin A protein, a key structural component of the cell nucleus. It can be employed in various biochemical and cell biology techniques, such as Western blotting, immunohistochemistry, and immunocytochemistry, to analyze the expression and localization of lamin A in different cell types and tissues.

Automatically generated - may contain errors

4 protocols using anti lamin a antibody

1

Isolating Nuclear Proteins for Western Blot

Check if the same lab product or an alternative is used in the 5 most similar protocols
Nuclear proteins were isolated as described before30 (link). Proteins (30 μg) were loaded on 5–12% Tris-acrylamide gels and subjected to western blotting, and the proteins were detected using antibody raised against β-catenin (Abcam Inc.); lamin A was used as an equal nuclear protein loading control and was detected using an anti-lamin A antibody (Sigma-Aldrich).
+ Open protocol
+ Expand
2

Chemical Compounds Characterization and Procurement

Check if the same lab product or an alternative is used in the 5 most similar protocols
Gemcitabine (purity > 98%), cycloheximide (purity > 93%) and MTT (purity > 98%) were purchased from Sigma-Aldrich (St. Louis, USA). LY294002 (purity > 98%) was purchased from Beyotime Institute of Biotechnology (Shanghai, China). Digoxin (purity > 97%), etoposide (purity > 99%), paclitaxel (purity > 99%), cisplatin (purity > 99%), 5-Fluorouracil (5-FU, purity > 99%), cytarabine (ara-C, purity > 99%), doxorubicin (purity > 99%) and MG132 (purity > 97%) were purchased from Selleck Chemicals (Houston, USA). Actinomycin D (purity > 95%) was purchased from KeyGen (Nanjing, China). Anti-NQO1, anti-HO-1 and anti-GCLC antibodies were obtained from Santa Cruz Biotechnology (Texas, USA). Anti-Keap1, anti-Nrf2, anti-p-Akt, anti-Akt, anti-p-P38 and anti-P38, anti-p-ERK1/2, anti-ERK1/2, anti-p-JNK and anti-JNK antibodies were purchased from Cell Signaling Technology (Danvers, USA). Anti-ABCC1 and anti-ABCC5 antibodies were purchased from ABclonal (Wuhan, China). Anti-β-actin and anti-ubiquitin antibodies were obtained from Bioworld (Minnesota, USA). Anti-lamin A antibody was obtained from Sigma-Aldrich (St. Louis, USA).
+ Open protocol
+ Expand
3

Western Blot Analysis of KDM1A Protein

Check if the same lab product or an alternative is used in the 5 most similar protocols
The eluted proteins in equal volume were separated by SDS-PAGE and transferred to semi-dry blotted polyvinylidene fluoride membranes (Bio-Rad). The membranes were probed with a rabbit polyclonal antibody against KDM1A (Cell Signaling Technology) or a rabbit polyclonal anti-lamin A antibody (Sigma Aldrich) to stain loading control, and then with horseradish peroxidase (HRP)-labeled secondary antibody (GE Healthcare, Tokyo, Japan). KDM1A bands were detected with Immobilon Western Chemiluminescent HRP substrate (Merck Millipore, Japan) using Image Quant LAS 4000 (GE Healthcare).
+ Open protocol
+ Expand
4

Separation of Nuclear and Cytoplasmic Proteins

Check if the same lab product or an alternative is used in the 5 most similar protocols
The nuclear and cytoplasma proteins were seperated as described before [28 (link)]. The protein was subjected to Western blotting and the blots were detected by using anti-H3K27Me3 (Cell Signaling Technology) and p65 (Santa Cruz Biotechnology), Lamin A or Histone H3 was used as an equal nuclear protein loading control and was detected by using an anti-Lamin A antibody (Sigma-Aldrich) or anti-Histone H3 (abcam) antibody.
+ 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!