Potassium Voltage-Gated Channel Subfamily E Member 1 (KCNE1) Antibody

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195€ (20 µl)

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935106861
info@markelab.com
name
Potassium Voltage-Gated Channel Subfamily E Member 1 (KCNE1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx001090
tested applications
ELISA, WB

Description

KCNE1 Antibody is a Rabbit Polyclonal antibody against KCNE1. The product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome. Alternatively spliced transcript variants encoding the same protein have been identified.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Potassium Voltage-Gated Channel Subfamily E Member 1 (KCNE1)
Host
Rabbit
Reactivity
Human, Mouse
Recommended Dilution
ELISA: 1 µg/ml, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
20 µl
Size 2
100 µl
Size 3
2 × 100 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P15382
Gene ID
3753
NCBI Accession
NP_000210.2
Background
Antibody anti-KCNE1
Status
RUO
Note
Concentration: > 0.2 mg/ml -

Descripción

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Potassium Voltage-Gated Channel Subfamily E Member 1 (KCNE1) Antibody

KCNE1 Antibody is a Rabbit Polyclonal antibody against KCNE1. The product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome. Alternatively spliced transcript variants encoding the same protein have been identified.

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