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Kv7.1 Antibody (S37A/10) [DyLight 350]

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Product Details

Summary
Reactivity Hu, Mu, Rt, HaSpecies Glossary
Applications WB, ICC/IF, IHC, IP, MA
Clone
S37A/10
Clonality
Monoclonal
Host
Mouse
Conjugate
DyLight 350

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Kv7.1 Antibody (S37A/10) [DyLight 350] Summary

Immunogen
Fusion protein amino acids 2-101 of human KCNQ1
Localization
Cell Membrane, Cytoplasmic Vesicle Membrane
Specificity
Detects approx 75 kDa.
Isotype
IgG1
Clonality
Monoclonal
Host
Mouse
Gene
KCNQ1
Purity
Protein G purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Immunocytochemistry/ Immunofluorescence
  • Immunohistochemistry
  • Immunoprecipitation
  • Microarray
  • Western Blot
Application Notes
Optimal dilution of this antibody should be experimentally determined.

Packaging, Storage & Formulations

Storage
Store at 4C in the dark.
Buffer
50mM Sodium Borate
Preservative
0.05% Sodium Azide
Purity
Protein G purified

Notes



DyLight (R) is a trademark of Thermo Fisher Scientific Inc. and its subsidiaries.

Alternate Names for Kv7.1 Antibody (S37A/10) [DyLight 350]

  • ATFB3
  • IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1
  • JLNS1
  • KCNA8
  • KCNA8FLJ26167
  • KCNA9
  • KCNA9Kv1.9
  • KCNQ1
  • kidney and cardiac voltage dependend K+ channel
  • KQT-like 1
  • Kv7.1
  • KVLQT1
  • KVLQT1ATFB1
  • 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

Background

KCNQ1 encodes a protein for a voltage-gated potassium channel required for the repolarization phase of the cardiac action potential. The gene product can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome, Romano-Ward syndrome, Jervell and Lange-Nielsen syndrome and familial atrial fibrillation. The gene is located in a region of chromosome 11 that contains a large number of contiguous genes that are abnormally imprinted in cancer and the Beckwith-Wiedemann syndrome. Two alternative transcripts encoding distinct isoforms have been described (from EntrezGene).

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Product General Protocols

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Video Protocols

WB Video Protocol
ICC/IF Video Protocol

FAQs for Kv7.1 Antibody (NBP2-12897UV) (0)

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Secondary Antibodies

 

Isotype Controls

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Research Areas for Kv7.1 Antibody (NBP2-12897UV)

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Bioinformatics

Gene Symbol KCNQ1