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Thermo Fisher Scientific SCNN1A Polyclonal Antibody
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Thermo Fisher Scientific SCNN1A Polyclonal Antibody

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SCNN1A 단백질을 인식하는 Rabbit Polyclonal 항체로, IHC에 적합합니다. Human 시료에 반응하며, 동결건조 형태로 제공됩니다. SCNN1A의 세포막 나트륨 채널 연구에 유용하며, 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 02. 오후 06:23
Thermo Fisher Scientific OSR00124W-100UL SCNN1A Polyclonal Antibody 100 ul pk판매 단위 pk ·
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563,100원VAT 포함 619,410원

Thermo Fisher Scientific · Thermo Fisher Scientific SCNN1A Polyclonal Antibody

Applications

Immunohistochemistry (IHC)


Product Specifications

항목 내용
Species Reactivity Human
Published Species Not Applicable
Host / Isotype Rabbit / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from the extracellular domain of human SCNN1A conjugated to an immunogenic 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.
  • Specificity: SCNN1A.

Target Information

Epithelial sodium channels (ENaC) are amiloride-sensitive members of the degenerin/epithelial sodium channel (Deg/ENaC) superfamily of ion channels. These channels share structural similarity, possessing two short intracellular amino and carboxyl termini, two membrane-spanning segments, and a large extracellular loop with a conserved cysteine-rich region.
There are three homologous isoforms of ENaC (α, β, γ). ENaC in the kidney, lung, and colon plays an essential role in trans-epithelial sodium and fluid balance. It also mediates aldosterone-dependent sodium reabsorption in the distal nephron, thus regulating blood pressure. ENaC function is partly regulated through association with the CFTR chloride channel.
Gain-of-function mutations in β- or γ-ENaC can cause severe arterial hypertension (Liddle’s syndrome), while loss-of-function mutations in α- or β-ENaC cause pseudohypoaldosteronism type I (PHA-1).


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

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