View primary antibody

Basic data

PID primary-0472
EPIC PID
Research group RG Hasenfuß
Quality (mean) no score (0.00)
Sharing level Public

Antibody data

Antigen symbol TRA-1-60
Antibody Registry ID(s) AB_778563
Name Anti-TRA-1-60 (R) antibody [TRA-1-60]
Alternative name TRA 1 60 antibody
Lab ID
Tag / Fluorophore
Raised in
Reacts with human
Clone TRA-1-60
Isotype IgM
Clonality monoclonal
Demasking unknown
Antigen Tissue/cells/virus corresponding to Human TRA-1-60 (R). Human embryonal carcinoma cell line 2102Ep cl.2A6.
Crafted By company
Company / Manufacturer Abcam
Catalog no. ab16288
Lot no.
Description WB Use a concentration of 1 - 10 µg/ml. Detects a band of approximately 250 kDa (predicted molecular weight: 235 kDa).
Localization Cell Membrane
Storage instruction Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Receipt date 2021-04-30 00:00:00
Preparation date 2021-04-30 00:00:00
Created by Klauenberg, Vanessa
Last modified Klauenberg, Vanessa

External links

Antibodypedia -
HGNC https://www.genenames.org/tools/search/#!/?query=TRA-1-60
Wikipedia https://en.wikipedia.org/wiki/TRA-1-60
Uniprot https://www.uniprot.org/uniprot/?query=TRA-1-60
GeneCards https://www.genecards.org/cgi-bin/carddisp.pl?gene=TRA-1-60
Antibody Registry https://antibodyregistry.org/search?q=AB_778563

Applications

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Linked publications

Caveolin3 Stabilizes McT1-Mediated Lactate/Proton Transport in Cardiomyocytes
Peper J et al.
Circ Res 2021: 10.1161/circresaha.119.316547
 
Generation of a genetically-modified induced pluripotent stem cell line harboring an oncogenic gene variant KRAS p.G12V
Busley AV et al.
Stem Cell Res 2023: 10.1016/j.scr.2023.103105
 
Generation of a genetically-modified induced pluripotent stem cell line harboring a Noonan syndrome-associated gene variant MRAS p.G23V
Busley AV et al.
Stem Cell Res 2023: 10.1016/j.scr.2023.103108
 
Generation of a pluripotent stem cell line (UMGi270-A) and a corresponding CRISPR/Cas9 modified isogenic control (UMGi270-A-1) from a patient with sudden onset dilated cardiomyopathy harboring a FLNC p.R2187P mutation
Maurer W et al.
Stem Cell Res 2024: 10.1016/j.scr.2024.103409
 
Mutation-induced LZTR1 polymerization provokes cardiac pathology in recessive Noonan syndrome
Busley AV et al.
Cell Rep 2024: 10.1016/j.celrep.2024.114448
 
Targeting Interleukin-8–Mediated Cellular Crosstalk Reverses Hypertrophic Cardiomyopathy and Cardiac Fibrosis in Noonan Syndrome
Fell J et al.
Circulation 2026: 10.1161/circulationaha.125.074155