Kv7.1 Knockout HeLa Cell Lysate


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Product Details

Reactivity HuSpecies Glossary
Applications WB

Order Details

Kv7.1 Knockout HeLa Cell Lysate Summary

Knockout achieved by using CRISPR/Cas9


Application Notes
You will receive 1 vial (100ug) of knockout cell lysate and 1 vial (100ug) of Parental cell lysate. Lysate can be diluted with 1X SDS sample buffer and will be stable at -20 degrees C for 12 months. Minimize freeze-thaw cycles.

Packaging, Storage & Formulations

Store at -20C short term. Aliquot and store at -80C long term. Avoid freeze-thaw cycles.
0.1 mg cell homogenate lyophilized in RIPA buffer made with double-knockout cell lines.
Reconstitution Instructions
To use as WB negative control, spin down briefly and resuspend in 100 uL 1xSDS sample buffer (2% SDS, 60 mM Tris-HCl pH 6.8, 10% Glycerol, 0.02% Bromophenol blue, 60 mM beta-mercaptoethanol). Boil the lysate for 3 - 5 minutes before loading it onto gel.

Lysate Details for Array

Knockout HeLa Cell


Powered by EDIGENE.
Validation of antibody specificity is critical and verification of antibody performance against knockout samples is one way to guarantee that an antibody recognizes a specific target. Novus' KO cell lysate can be used as a negative control for western blots and to confirm the specificity of antibodies.

Alternate Names for Kv7.1 Knockout HeLa Cell Lysate

  • ATFB3
  • IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1
  • JLNS1
  • KCNA8FLJ26167
  • KCNA9Kv1.9
  • kidney and cardiac voltage dependend K+ channel
  • KQT-like 1
  • Kv7.1
  • LQT
  • LQT1
  • potassium voltage-gated channel subfamily KQT member 1
  • potassium voltage-gated channel, KQT-like subfamily, member 1
  • RWS
  • slow delayed rectifier channel subunit
  • SQT2
  • Voltage-gated potassium channel subunit Kv7.1
  • WRS


This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]


This product is for research use only and is not approved for use in humans or in clinical diagnosis. Lysates are guaranteed for 6 months from date of receipt.

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Gene Symbol KCNQ1