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Thermo Fisher Scientific SCNN1B Monoclonal Antibody (7B8), FITC
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Thermo Fisher Scientific SCNN1B Monoclonal Antibody (7B8), FITC

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SCNN1B 단백질을 인식하는 Mouse 모노클로날 항체로 FITC 형광 표지된 제품입니다. Western blot과 IHC에 사용 가능하며, ENaC beta 단백질 검출에 최적화되어 있습니다. 단백질 G 정제, 액상 형태로 4°C 암소 보관합니다.

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마지막 업데이트 2025. 07. 26. 오전 08:26
Thermo Fisher Scientific MA545353 SCNN1B Monoclonal Antibody (7B8), FITC 100 ug pk판매 단위 pk ·
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663,800원VAT 포함 730,180원

Thermo Fisher Scientific · Thermo Fisher Scientific SCNN1B Monoclonal Antibody (7B8), FITC

Thermo Fisher Scientific SCNN1B Monoclonal Antibody (7B8), FITC

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:1,000
Immunohistochemistry (IHC) 1:150

Product Specifications

항목 내용
Species Reactivity Mouse
Host/Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 7B8
Immunogen Synthetic peptide from the C-terminal of Rat ENaC beta (aa. 617-638)
Conjugate FITC
Excitation/Emission Max 498/517 nm
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer 9.1mM sodium bicarbonate/PBS, pH 7.4, with 640.91mM DMSO, 136.36mM ethanolamine
Contains No preservative
Storage Conditions 4°C, store in dark
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2931807

Additional Formats

Product Specific Information

A 1:1,000 dilution of MA5-45353 was sufficient for detection of ENaC beta in 15 µg of Mouse whole kidney lysate by ECL immunoblot analysis using goat anti-mouse IgG:HRP as the secondary antibody. Detects approximately 87 kDa.

Target Information

Sodium permeable non-voltage-sensitive ion channel inhibited by the diuretic amiloride. Mediates electrodiffusion of luminal sodium (and water, which follows osmotically) through the apical membrane of epithelial cells. Controls sodium reabsorption in kidney, colon, lung, and sweat glands, and plays a role in taste perception.

Forms heterotetramer of two alpha, one beta, and one gamma subunit (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) and Liddle syndrome, both related to sodium channel dysfunction.

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

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