CacheBy
Thermo Fisher Scientific SCNN1B Monoclonal Antibody (16E4), APC
원본

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

상품 한눈에 보기

SCNN1B 단백질을 인식하는 마우스 단클론 항체로, APC로 결합되어 형광 분석에 적합합니다. Western blot에 1:1,000 희석으로 사용 가능하며, 뇌, 신장 등에서의 ENaC β 단백질 검출에 유용합니다. 단백질 G로 정제된 액상 형태로 4°C에서 보관합니다.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 07. 29. 오후 02:22
Thermo Fisher Scientific MA545355 SCNN1B Monoclonal Antibody (16E4), APC 100 ug pk판매 단위 pk ·
재고 확인 필요
663,800원VAT 포함 730,180원

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

Applications and Tested Dilution

  • Western Blot (WB): 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 APC (Allophycocyanin)
Excitation / Emission Max 651 / 660 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_2931809

Additional Formats

Product Specific Information

A 1:1,000 dilution of MA5-45355 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 osmotically following water) through the apical membrane of epithelial cells. Controls sodium reabsorption in kidney, colon, lung, and sweat glands, and also 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.

Defects in SCNN1B cause:

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

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

제품 이미지

spectra

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.