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Thermo Fisher Scientific FOXC1 Polyclonal Antibody
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Thermo Fisher Scientific FOXC1 Polyclonal Antibody

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FOXC1 단백질을 인식하는 Rabbit Polyclonal 항체로, Human 및 Mouse 시료에서 검증됨. Western blot, ICC/IF, ChIP assay에 사용 가능. 합성 펩타이드 기반 면역원으로 제작되었으며, 항원 친화 크로마토그래피로 정제됨. 연구용으로만 사용.

카탈로그번호
PA1807
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 09:15
Thermo Fisher Scientific PA1807 FOXC1 Polyclonal Antibody 100 ug pk판매 단위 pk ·
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617,800원VAT 포함 679,580원

Thermo Fisher Scientific · Thermo Fisher Scientific FOXC1 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 1:500 View 3 publications
Immunocytochemistry (ICC/IF) 2 µg/mL -
ChIP assay (ChIP) 1–3 µg × 10⁶ cells View 2 publications

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Published Species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to residues A(423) V D D P L P D Y S L P(434) of human FOXC1
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with 1 mg/mL BSA
Contains 0.05% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2247078

Product Specific Information

PA1-807 detects FOXC1 from human and mouse samples.
It has been successfully used in Western blot procedures.
By Western blot, PA1-807 detects a ~50 kDa band representing FOXC1 from HepG2 cells and mouse kidney cells.
This antibody also detects a nonspecific band at ~45 kDa from HepG2 cells, and at ~60 kDa from mouse kidney samples.

The immunogen is a synthetic peptide corresponding to residues A(423) V D D P L P D Y S L P(434) of human FOXC1.
PA1-807 can be used with blocking peptide PEP-298.


Target Information

FOXC1 is a protein belonging to the forkhead family of transcription factors characterized by a distinct DNA-binding forkhead domain.
It plays a role in regulating the FGF19–FGFR4–MAPK pathway, promoting the development and maintenance of anterior segment structures within the eye.
Mutations in this gene are associated with various ocular disorders such as glaucoma, iridogoniodysgenesis anomaly, Peters anomaly, and Axenfeld-Rieger anomaly.


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

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