CacheBy
Thermo Fisher Scientific CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Monoclonal Antibody (CFTR, 1643)
원본

Thermo Fisher Scientific CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Monoclonal Antibody (CFTR, 1643)

상품 한눈에 보기

CFTR 단백질을 표적하는 Thermo Fisher Scientific의 단클론 항체로, 인간 시료에 반응합니다. IHC, Flow Cytometry, Peptide Array 등 다양한 응용에 적합하며, Protein A/G로 정제된 액상 형태입니다. 연구용으로만 사용 가능합니다.

카탈로그번호
1080-MSM3-P1
판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 03. 오후 03:29
Thermo Fisher Scientific 1080-MSM3-P1 CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Monoclonal Antibody (CFTR, 1643) 100 ug pk판매 단위 pk
재고 1개
825,100원VAT 포함 907,610원

Thermo Fisher Scientific · Thermo Fisher Scientific CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Monoclonal Antibody (CFTR, 1643)

Thermo Fisher Scientific CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Monoclonal Antibody (CFTR, 1643)

Applications and Tested Dilution

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC (P)) 1–2 µg/mL
Flow Cytometry (Flow) 1–2 µg/10^6 cells
Peptide Array (Array) Assay-dependent

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone CFTR, 1643
Immunogen Recombinant fragment (around aa 258–385) of human CFTR protein
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Immunohistochemistry (PFA fixed): Incubate antibody for 30 minutes at room temperature.
  • Staining of formalin-fixed tissues requires heating tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 45 minutes at 95°C, followed by cooling at room temperature for 20 minutes.

Target Information

Cystic Fibrosis (CF) is a common lethal genetic disease caused by mutations in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-regulated chloride channel. Approximately 70% of CF cases involve deletion of phenylalanine at position 508 (ΔF508), leading to abnormal chloride transport.
CF typically results in severe lung and liver disease. Interestingly, CFTR also serves as an entry point for Salmonella typhi into intestinal epithelial cells, and ΔF508 heterozygous and homozygous mice show 86% and 100% reductions in S. typhi intestinal submucosal uptake, respectively.

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

제품 이미지

(이미지 없음)

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.