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Thermo Fisher Scientific SCNN1B Monoclonal Antibody (16E4), FITC
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Thermo Fisher Scientific SCNN1B Monoclonal Antibody (16E4), FITC

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SCNN1B 단백질을 인식하는 FITC 결합 단일클론 항체. Western blot에서 1:1,000 희석으로 사용 가능. Protein G 정제 및 무보존제 액상 형태. 4°C 암소 보관, 연구용 전용. 다양한 형광 표지 형식 제공.

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마지막 업데이트 2025. 08. 04. 오후 03:01
Thermo Fisher Scientific MA545356 SCNN1B Monoclonal Antibody (16E4), FITC 100 ug pk판매 단위 pk ·
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663,800원VAT 포함 730,180원

Thermo Fisher Scientific · Thermo Fisher Scientific SCNN1B Monoclonal Antibody (16E4), FITC

Applications and Tested Dilution

  • Application: Western Blot (WB)
  • Tested Dilution: 1:1,000

Product Specifications

항목 내용
Species Reactivity Mouse
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone 16E4
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 9.1 mM sodium bicarbonate/PBS (pH 7.4) with 640.91 mM DMSO, 136.36 mM ethanolamine
Contains No preservative
Storage Conditions 4°C, store in dark
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2931810

Available Formats

  • APC (Cat. MA5-45355)
  • PerCP (Cat. MA5-45357)
  • Custom conjugation available upon request

Product Specific Information

A 1:1,000 dilution of MA5-45356 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 through the apical membrane of epithelial cells, controlling sodium reabsorption in kidney, colon, lung, and sweat glands. Plays a role in taste perception.

The channel is a heterotetramer 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.

Associated Diseases:

  • Autosomal recessive pseudohypoaldosteronism type 1 (PHA1)
  • Liddle syndrome (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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