6-CFDA N-succinimidyl ester
CAS No. 150206-15-8
6-CFDA N-succinimidyl ester( —— )
Catalog No. M17327 CAS No. 150206-15-8
The succinimidyl ester group is capable of spontaneously and irreversibly binding to free amines. Utilized in flow cytometry experiments for tracking cell division in both mammalian cells and bacteria.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 85 | In Stock |
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| 2MG | 29 | In Stock |
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| 5MG | 58 | In Stock |
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| 10MG | 93 | In Stock |
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| 25MG | 147 | In Stock |
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| 50MG | 253 | In Stock |
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| 100MG | 373 | In Stock |
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| 200MG | 528 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name6-CFDA N-succinimidyl ester
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NoteResearch use only, not for human use.
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Brief DescriptionThe succinimidyl ester group is capable of spontaneously and irreversibly binding to free amines. Utilized in flow cytometry experiments for tracking cell division in both mammalian cells and bacteria.
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DescriptionThe succinimidyl ester group is capable of spontaneously and irreversibly binding to free amines. Utilized in flow cytometry experiments for tracking cell division in both mammalian cells and bacteria. Used in combination with several cell permeabilizers as an effective, nondestructive fluorescencent stain to quickly detect bacterial cells.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayMAPK/ERK Signaling
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TargetJNK
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number150206-15-8
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Formula Weight557.47
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Molecular FormulaC29H19NO11
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(=O)Oc5cc6Oc1cc(ccc1C3(OC(=O)c2ccc(cc23)C(=O)ON4C(=O)CCC4=O)c6cc5)OC(C)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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BSJ-04-122
BSJ-04-122 is a covalent dual inhibitor of MKK4 and MKK7, demonstrating IC50 values of 4 nM and 181 nM, respectively. [BSJ-04-122] can be used for cancer research.
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c-JUN peptide
Peptide comprising residues 33 - 57 of the JNK binding (δ) domain of human c-Jun. Disrupts JNK/c-Jun interaction leading to inhibition of serum-induced c-Jun phosphorylation, up-regulation of p21cip/waf and modulation of inflammatory gene expression. Specifically induces apoptosis in HeLa tumor cells.
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d-Epigalbacin
d-Epigalbacin is a naturally occurring lignin. d-Epigalbacin is a potent, selective JNKs inhibitor, with IC50s of 1.7 μM, 2.9 μM and 1.74 μM for JNK1, JNK2 and JNK3, respectively.
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