ARG45617

anti-KCNQ2 antibody

anti-KCNQ2 antibody for Flow cytometry,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse,Rat

Overview

Product Description Rabbit Polyclonal antibody recognizes KCNQ2
Tested Reactivity Hu, Ms, Rat
Tested Application FACS, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name KCNQ2
Antigen Species Human
Immunogen Recombinant protein containing to human KCNQ2.
Conjugation Un-conjugated
Alternate Names KCNQ2; Potassium Voltage-Gated Channel Subfamily Q Member 2; KCNA11; Kv7.2; HNSPC; ENB1; BFNC; Potassium Channel, Voltage Gated KQT-Like Subfamily Q, Member 2; Neuroblastoma-Specific Potassium Channel Subunit Alpha KvLQT2; Potassium Voltage-Gated Channel Subfamily KQT Member 2; Voltage-Gated Potassium Channel Subunit Kv7.2; EBN1; EBN; Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 2; KQT-Like 2; DEE7

Application Instructions

Application Suggestion
Tested Application Dilution
FACS1 - 3 µg/10^6 cells
IHC-P2-5 μg/ml
WB0.25-0.5 μg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 97 kDa

Properties

Form Liquid
Purification Affinity purified
Buffer 0.2% Na2HPO4, 0.9% NaCl and 4% Trehalose.
Stabilizer 4% Trehalose
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 16536 Mouse KCNQ2

GeneID: 170848 Rat KCNQ2

GeneID: 3785 Human KCNQ2

Gene Symbol KCNQ2
Gene Full Name Potassium Voltage-Gated Channel Subfamily Q Member 2
Background The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Function Pore-forming subunit of the voltage-gated potassium (Kv) M-channel which is responsible for the M-current, a key controller of neuronal excitability. [UniProt]
Cellular Localization Cell membrane. [UniProt]
Calculated MW 96 kDa
PTM Phosphoprotein; Ubl conjugation. [UniProt]

Images (5) Click the Picture to Zoom In

  • ARG45617 anti-KCNQ2 antibody IHC-P image

    Immunohistochemistry: Human breast cancer stained with ARG45617 anti-KCNQ2 antibody at 2 μg/ml dilution.

  • ARG45617 anti-KCNQ2 antibody WB image

    Western blot: HEK293 stained with ARG45617 anti-KCNQ2 antibody at 0.5 μg/ml dilution.

  • ARG45617 anti-KCNQ2 antibody FACS image

    Flow Cytometry: 293T stained with ARG45617 anti-KCNQ2 antibody at 1 µg/10^6 cells dilution.

  • ARG45617 anti-KCNQ2 antibody WB image

    Western blot: Rat brain stained with ARG45617 anti-KCNQ2 antibody at 0.5 μg/ml dilution.

  • ARG45617 anti-KCNQ2 antibody WB image

    Western blot: Mouse brain stained with ARG45617 anti-KCNQ2 antibody at 0.5 μg/ml dilution.