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Thermo Fisher Scientific KCNH2 Polyclonal Antibody
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Thermo Fisher Scientific KCNH2 Polyclonal Antibody

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Thermo Fisher Scientific의 KCNH2 Polyclonal Antibody는 인간, 마우스, 랫트 시료에 반응하며 WB 및 IHC(P) 실험에 적합합니다. 합성 펩타이드 항원으로 제작된 비결합형 항체로, 장기 보관 시 -20°C에서 안정적으로 유지됩니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 04. 오후 04:22
Thermo Fisher Scientific OSP00150W-100UL KCNH2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
563,100원VAT 포함 619,410원

Thermo Fisher Scientific · Thermo Fisher Scientific KCNH2 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 1:1,000–1:2,000 -
Immunohistochemistry (Paraffin) (IHC (P)) 1:3,000 -
Miscellaneous PubMed (Misc) - View 2 publications

Product Specifications

Specification Details
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from aa region 1120–1162 of mouse KCNH2 conjugated to blue carrier protein
Conjugate Unconjugated
Form Lyophilized
Concentration Not Determined
Storage Buffer Whole serum
Contains No preservative
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. Glycerol (1:1) may be added for added stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
  • The peptide is homologous in rat and human.
  • Specificity of this antibody: KCNS2.

Target Information

Human ether-a-go-go related gene (HERG) encodes the pore-forming alpha subunit of the delayed rectifier potassium channel IKr.
There are two N-terminal splice variants of HERG: 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 1 alpha.
Residues within the C-terminal play a role in channel expression and gating, including voltage-dependent activation.
HERG is expressed in the heart, more abundantly in ventricles than atria.
Mutations in HERG increase beat-to-beat variability and early after depolarization, contributing to long QT syndrome type 2 and short QT syndrome type 1.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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