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Thermo Fisher Scientific Phospho-SCNN1B (Ser633) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-SCNN1B (Ser633) Polyclonal Antibody

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SCNN1B 단백질의 Ser633 인산화 부위를 인식하는 다클론 항체로, IHC에 최적화되어 있습니다. 쥐 및 랫트 반응성이 있으며, 동결건조 형태로 제공됩니다. 연구용으로만 사용되며 장기 보관 시 -20°C에서 안정적입니다.

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마지막 업데이트 2025. 08. 05. 오후 03:05
Thermo Fisher Scientific OSS00145W-100UL Phospho-SCNN1B (Ser633) Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
563,100원VAT 포함 619,410원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-SCNN1B (Ser633) Polyclonal Antibody

Thermo Fisher Scientific Phospho-SCNN1B (Ser633) Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Immunohistochemistry (IHC) 1:300–1:2,000

Publications


Product Specifications

항목 내용
Species Reactivity Mouse, Rat
Published Species Not Applicable
Host / Isotype Sheep / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide to phospho S633 of rat amiloride-sensitive sodium channel subunit beta (SCNN1B, SCNEB) 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.
  • The antigen is homologous with the corresponding sequence in mouse.
  • Specificity: SCNN1B.

Target Information

Sodium permeable non-voltage-sensitive ion channel inhibited by the diuretic amiloride. Mediates electrodiffusion of luminal sodium (and water) through epithelial cell apical membranes. Controls sodium reabsorption in kidney, colon, lung, and sweat glands, and plays a role in taste perception.
Forms a heterotetramer of two alpha, one beta, and one gamma subunit; a delta subunit can replace the alpha subunit.
Interacts with WW domains of NEDD4, NEDD4L, WWP1, and WWP2.

Defects in SCNN1B cause:

  • Autosomal recessive pseudohypoaldosteronism type 1 (PHA1) – a rare salt-wasting disease due to mineralocorticoid unresponsiveness.
  • Liddle syndrome – an autosomal dominant pseudoaldosteronism with hypertension and hypokalemic alkalosis.

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

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