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D4813

Sigma-Aldrich

Dendrotoxin-K

≥98% (HPLC), lyophilized powder

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About This Item

MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77

Quality Level

assay

≥98% (HPLC)

form

lyophilized powder

mol wt

6,542 Da

storage temp.

−20°C

Related Categories

Application

Dendrotoxin-K is suitable for use as a potassium voltage-gated channel subfamily A member 1 (Kv1.1) channel blocker in axon and human embryonic kidney (HEK293) cells. It has also been used as a selective blocker of Kv channels in mice.

Biochem/physiol Actions

Dendrotoxin-K (DTXk) is isolated from mamba snake Dendroaspis polylepis and interacts with the β-turn region in the N-terminal sequence of the potassium channel. It inhibits tumor progression in gefitinib-resistant non-small cell lung cancer cells. DTXk induces neuronal damage in the hippocampus via N-methyl-d-aspartate (NMDA) and non-NMDA receptors.
Dendrotoxin-K inhibits potassium channels that contain Kv1.1 protein only.

Features and Benefits

This compound is featured on the Potassium Channels page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Other Notes

Isolated initially from Dendroaspis polylepis polylepis venom

Preparation Note

Purified by a modification of the method of Schweitz.

Reconstitution

Reconstitute in 1 mL deionized water or buffer (pH 7.5) to yield 10 μM stock

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Analog modulation of spike-evoked transmission in CA 3 circuits is determined by axonal K v1. 1 channels in a time-dependent manner
Bialowas A, et al.
The European Journal of Neuroscience, 41(3), 293-304 (2015)
F C Wang et al.
European journal of biochemistry, 263(1), 222-229 (1999-08-03)
Dendrotoxin (DTX) homologues are powerful blockers of K+ channels that contain certain subfamily Kv1 (1.1-1.6) alpha- and beta-subunits, in (alpha)4(beta)4 stoichiometry. DTXk inhibits potently Kv1.1-containing channels only, whereas alphaDTX is less discriminating, but exhibits highest affinity for Kv1.2. Herein, the
Effects of voltage-gated K+ channel blockers in gefitinib-resistant H460 non-small cell lung cancer cells
Jeon WIL, et al.
Anticancer Research, 32(12), 5279-5284 (2012)
Identification of residues in dendrotoxin K responsible for its discrimination between neuronal K+ channels containing Kv1. 1 and 1.2 alpha subunits
Wang FC, et al.
European Journal of Biochemistry, 263(1), 222-229 (1999)
Cav1. 3 calcium channels are required for normal development of the auditory brainstem
Hirtz JJ, et al.
The Journal of Neuroscience, 31(22), 8280-8294 (2011)

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