Home - Products - Others - Other Targets - Ethidium bromide

Ethidium bromide

CAS No. 1239-45-8

Ethidium bromide ( —— )

Catalog No. M10965 CAS No. 1239-45-8

A trypanocidal agent and possible antiviral agent that is widely used in experimental cell biology and biochemistry.

Purity : >98%(HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

Size	Price / USD	Stock	Quantity
10MG	57	In Stock
25MG	102	In Stock
50MG	144	In Stock
100MG	Get Quote	In Stock
200MG	Get Quote	In Stock
500MG	Get Quote	In Stock
1G	Get Quote	In Stock

Group Booking Get Quotation Bulk Inquiry Add to Cart

Biological Information

Product Name

Ethidium bromide
Note

Research use only, not for human use.
Brief Description

A trypanocidal agent and possible antiviral agent that is widely used in experimental cell biology and biochemistry.
Description

A trypanocidal agent and possible antiviral agent that is widely used in experimental cell biology and biochemistry. Ethidium has several experimentally useful properties including binding to nucleic acids, noncompetitive inhibition of nicotinic acetylcholine receptors, and fluorescence among others. It is most commonly used as the bromide.
Synonyms

——
Pathway

Others
Target

Other Targets
Recptor

Others
Research Area

——
Indication

——

Chemical Information

CAS Number

1239-45-8
Formula Weight

394.32
Molecular Formula

C21H20BrN3
Purity

>98%(HPLC)
Solubility

DMSO: 10 mM
SMILES

[Br-].CC[N+]1=C2C=C(N)C=CC2=C2C=CC(N)=CC2=C1C1=CC=CC=C1
Chemical Name

——

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

1.Diaz F, et al. Nucleic Acids Res. 2002 Nov 1;30(21):4626-33.

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

7,3,4-Tri-O-methyler...

7, 3',4'-Tri-O-methyleriodictyol has antimutagenic activity.
Papain

Papain is a cysteine protease of the peptidase C1 family. Papain is used in food, pharmaceutical, textile, and cosmetic industries.
Urantide

Selective and competitive urotensin-II (UT) receptor antagonist (pKB = 8.3). Blocks hU-II induced contractions in thoracic aorta ex vivo. Exhibits no effect on noradrenaline or endothelin 1-induced contraction or on acetylcholine-induced relaxation. Behaves as a partial agonist in a calcium mobilization assay (in CHO cells expressing hUT receptors).

Sign In Join Free