Cookie Policy: This site uses cookies to improve your experience. You can find out more about our use of cookies in our Privacy Policy. By continuing to browse this site you agree to our use of cookies.
Bertin Bioreagent
anti-TRAP220, mAb (1A10)
As low as
777
CHF
CHF 777.00
In stock
Only %1 left
BRT-G01041-R100100 µlCHF 777.00

Product Details | |
---|---|
Synonyms | MED1; Mediator Subunit 1; Mediator of RNA Polymerase II Transcription Subunit 1; Thyroid Hormone Receptor-associated Protein Complex 220 kDa Component; TRIP-2 |
Product Type | Monoclonal Antibody |
Properties | |
Clone | 1A10 |
Isotype | Mouse IgG1κ |
Source/Host | Mouse |
Immunogen/Antigen | Synthetic peptide. |
Application | ELISA, Western Blot, Immunoprecipitation, Immunofluorescence. Recommended dilutions: 1/500-1/5000 |
Specificity | Recognizes human TRAP220. |
Formulation | Liquid. Does not contain any preservative. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
Declaration | Manufactured by Bertin Bioreagent |
Shipping and Handling | |
Shipping | BLUE ICE |
Long Term Storage | -20°C |
Handling Advice | Avoid freeze/thaw cycles. |
Use/Stability | Stable for at least 3 years after receipt when stored at -20°C. |
Documents | |
Product Specification Sheet | |
Datasheet |
![]() |
Description
TRAP220 is a scaffold protein in the Mediator complex, helping recruit RNA polymerase II to target genes. TRAP220 specifically interacts with nuclear receptors such as thyroid hormone receptor (TR), retinoid X receptor (RXR), peroxisome proliferator-activated receptor (PPAR) and estrogen receptor (ER). It enhances ligand-dependent transcription of these receptors. TRAP220 helps in histone modification, making DNA more accessible for transcription. TRAP220/MED1 is overexpressed in breast and prostate cancers, contributing to hormone-driven tumor growth. Since TRAP220 interacts with PPARs, it is involved in glucose metabolism and obesity-related pathways. Mutations in TRAP220 can lead to embryonic lethality and growth defects due to disrupted nuclear receptor signaling.