K0640

Anti-Potassium Channel Kv11.1 (HERG) Extracellular−FITC antibody produced in rabbit

affinity isolated antibody, lyophilized powder

Manufacturer: Sigma Aldrich

Synonym(S): Anti-KCNH2, Anti-Voltage gated K+ channel subfamily H member 2, Anti-ether-a-go-go-related channel 1

Select a Size

Pack Size SKU Availability Price
50 μL K0640-50-μL In Stock ₹ 41,791.50

K0640 - 50 μL

₹ 41,791.50

In Stock

Quantity

1

Base Price: ₹ 41,791.50

GST (18%): ₹ 7,522.47

Total Price: ₹ 49,313.97

biological source

rabbit

Quality Level

200

conjugate

FITC conjugate

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

lyophilized powder

species reactivity

human

technique(s)

flow cytometry: 2-10 μg/mL using 1x106 human live cellsimmunocytochemistry: 1:25 using intact live HEK-KV11.1 transfected cells

UniProt accession no.

Q12809

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Description

  • General description: Anti-Potassium Channel KV11.1 (HERG)- Extracellular-FITC (Voltage gated K+ channel subfamily H member 2, KCNH2, ether-a-go-go-related channel 1) is produced in rabbit using as immunogen the peptide AFLLKETEEGPPATEC corresponding to residues 430-445 of human KV11.1 (HERG). Anti-KV11.1 (HERG) antibody is directed against an extracellular epitope located between the S1 and S2 domains. The antibody is affinity purified on immobilized antigen and labeled with fluorescein isothiocyanate (FITC).
  • Immunogen: peptide AFLLKETEEGPPATEC corresponding to residues 430-445 of human KV11.1 (HERG).
  • Application: Flow cytometry: a recommended working concentration of 2-10 μg per 1x106cells was determined using intact live human cells.
  • Biochem/physiol Actions: The gene Kv11.1, also referred to as HERG (human ether-a-go-go related gene), encodes the α-subunit of the rapid component of the delayed rectifier potassium channel. The third repolarization of the action potential of human cardiomyocytes is carried out by this protein. Mutations in this gene have been associated with type II hereditary long QT syndrome (LQT2). This disease is characterized by prolongation of the QT interval, abnormal T wave, torsade de pointes, syncope and sudden death caused by cardiac arrest.
  • Physical form: Lyophilized from phosphate buffered saline, pH 7.4, containing 1% BSA and 0.05% sodium azide.
  • Reconstitution: Reconstitute the lyophilized vial with 50 μL or 200 μL deionized water, depending on package size. Further dilutions should be made using a carrier protein such as BSA (1-3%).
  • Other Notes: Lyophilized powder can be stored intact at room temperature for several weeks. For extended storage, it should be stored at -20 °C or below. The reconstituted solution can be stored at 2-8 °C for up to 2 weeks. For longer storage, freeze in working aliquots. Avoid repeated freezing and thawing. Storage in “frost-free” freezers is not recommended. Centrifuge before use. Working dilution samples should be discarded if not used within 12 hours. The antibody is stable for at least 12 months when stored appropriately.
  • Disclaimer: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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affinity isolated antibody, lyophil...


biological source:
rabbit

Quality Level:
200

conjugate:
FITC conjugate

antibody form:
affinity isolated antibody

antibody product type:
primary antibodies

clone:
polyclonal

form:
lyophilized powder

species reactivity:
human

technique(s):
flow cytometry: 2-10 μg/mL using 1x106 human live cellsimmunocytochemistry: 1:25 using intact live HEK-KV11.1 transfected cells

UniProt accession no.:
Q12809

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