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Kv11.1 Antibody

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Western Blot: Kv11.1 Antibody [NBP3-10366] - Western blot analysis using NBP3-10366 on Human OVCAR-3 as a positive control. Antibody Titration: 0.2-1 ug/ml

Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB
Clonality
Polyclonal
Host
Rabbit
Conjugate
Unconjugated
Concentration
0.5 mg/ml

Order Details

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Kv11.1 Antibody Summary

Immunogen
The immunogen is a synthetic peptide directed towards the C-terminal region of human Kv11.1 (NP_742054). Peptide sequence SQVSQFMACEELPPGAPELPQEGPTRRLSLPGQLGALTSQPLHRHGSDPG
Clonality
Polyclonal
Host
Rabbit
Gene
KCNH2
Purity
Affinity purified
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Applications/Dilutions

Dilutions
  • Western Blot 1.0 ug/ml
Theoretical MW
90 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS, 2% Sucrose
Preservative
0.09% Sodium Azide
Concentration
0.5 mg/ml
Purity
Affinity purified

Alternate Names for Kv11.1 Antibody

  • Eag homolog
  • Eag-related protein 1
  • ERG
  • ERG1
  • ERG-1
  • Ether-a-go-go-related gene potassium channel 1
  • ether-a-go-go-related potassium channel protein
  • Ether-a-go-go-related protein 1
  • HERG
  • H-ERG
  • hERG1
  • hERG-1
  • HERGhERG-1
  • KCNH2
  • Kv11.1
  • LQT2
  • potassium voltage-gated channel subfamily H member 2
  • potassium voltage-gated channel, subfamily H (eag-related), member 2
  • SQT1
  • Voltage-gated potassium channel subunit Kv11.1

Background

Human ether-a-go-go related gene (HERG) encodes the pore-forming subunit of the delayed rectifier potassium channel IKr. There are two N-terminal splice variants of HERG include the full-length isoform 1 alpha and the shorter isoform 1 beta. Isoform 1 beta lacks the PAS motif and deactivates at a faster rate than isoform 1alpha. Residues within the C-terminal play a role in channel expression and channel gating, including voltage-dependent activation. HERG is expressed in the heart and is more abundantly expressed in the ventricles than in the atria. Mutations in the gene encoding HERG increase beat-to-beat variability and early after depolarization. These fluctuations facilitate the genesis and propagation of premature heartbeats associated with inheritable long QT syndrome type 2 and short QT syndrome type 1.

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

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol KCNH2