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Thermo Fisher Scientific SCNN1B Polyclonal Antibody
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Thermo Fisher Scientific SCNN1B Polyclonal Antibody

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SCNN1B 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체. Western blot에 최적화되어 있으며, 인간 시료에 반응. 항원 친화 크로마토그래피로 정제된 액상 제품으로, 4°C 단기 보관 및 -20°C 장기 보관 권장.

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마지막 업데이트 2025. 08. 02. 오전 01:55
Thermo Fisher Scientific PA528909 SCNN1B Polyclonal Antibody 100 ul pk판매 단위 pk ·
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699,000원VAT 포함 768,900원

Thermo Fisher Scientific · Thermo Fisher Scientific SCNN1B Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:3,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fragment corresponding to a region within amino acids 119–332 of Human betaENaC
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage buffer 0.1M Tris glycine, pH 7, with 10% glycerol
Contains 0.01% thimerosal
Storage conditions Store at 4°C short term. For long-term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions Wet ice
RRID AB_2546385

Product Specific Information

  • Recommended positive controls: 293T, A431, H1299, HeLa, HepG2, Molt-4, Raji
  • Predicted reactivity: Dog (82%), Guinea pig (80%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

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

Defects in SCNN1B cause autosomal recessive pseudohypoaldosteronism type 1 (PHA1) [MIM:264350], a rare salt-wasting disease due to organ unresponsiveness to mineralocorticoids. PHA1 presents in neonates with dehydration, hyponatremia, hyperkalemia, metabolic acidosis, and failure to thrive.
Defects in SCNN1B also cause Liddle syndrome, an autosomal dominant disorder characterized by pseudoaldosteronism and hypertension associated with hypokalemic alkalosis, due to constitutive activation of the renal epithelial sodium channel.

WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.

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

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