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

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SCNN1B 단백질을 인식하는 PerCP 결합 단일클론 항체로, Western blot 및 IHC에 최적화되어 있습니다. 마우스 반응성, IgG1 아이소타입, Protein G 정제, 4°C 보관 조건. 나트륨 채널 연구 및 신장, 폐, 대장 조직 분석에 적합.

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마지막 업데이트 2025. 08. 05. 오전 03:41
Thermo Fisher Scientific MA545354 SCNN1B Monoclonal Antibody (7B8), PerCP 100 ug pk판매 단위 pk ·
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663,800원VAT 포함 730,180원

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

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

Applications and Tested Dilution

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

Product Specifications

Specification Detail
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 PerCP
Excitation / Emission Max 482 / 675 nm
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer 95.64 mM phosphate / 2.48 mM MES, pH 7.4, with 0.5 M EDTA
Contains No preservative
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2931808

Additional Formats

Product Specific Information

A 1:1,000 dilution of MA5-45354 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 the 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 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) and Liddle syndrome, both involving abnormal sodium channel regulation.

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

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