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Thermo Fisher Scientific FGFR2 Polyclonal Antibody
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Thermo Fisher Scientific FGFR2 Polyclonal Antibody

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FGFR2 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, Human 및 Mouse 반응성. Western blot, IHC에 적합하며 FGFR1/FGFR3 교차반응 없음. 항원 친화 크로마토그래피 정제, 1.3 mg/mL 농도, PBS/BSA 버퍼에 보관.

카탈로그번호
PA124763
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 04:26
Thermo Fisher Scientific PA124763 FGFR2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
640,300원VAT 포함 704,330원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR2 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 0.25–0.5 µg/mL View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 2–4 µg/mL View 1 publication
Immunoprecipitation (IP) View 1 publication

Product Specifications

Specification Description
Species Reactivity Human, Mouse
Published Species Mouse, Non-human primate
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide conjugated to KLH by a Glutaraldehyde linker, corresponding to residues K(809)-T(821) of the cytoplasmic region of Human FGFR2
Conjugate Unconjugated
Form Liquid
Concentration 1.3 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.4, with 1% BSA
Contains 15 mM sodium azide
Storage Conditions Store at 4°C short term; for long-term storage, store at -20°C, avoiding freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_780623

Product Specific Information

This antibody shows no cross-reactivity with FGFR1 or FGFR3.
PA1-24763 is expected to cross-react with mouse (92% conserved) and rat (92% conserved) due to sequence homology.


Target Information

FGFR2 is a member of the FGFR family of receptor tyrosine kinases. This family regulates cellular functions such as angiogenesis, mitogenesis, osteogenesis, myogenesis, carcinogenesis, differentiation, and tissue repair.
FGFR family members are implicated in diseases including cancer, rheumatoid arthritis, and diabetic retinopathy. Mutations in FGFR2 are associated with several syndromes such as Crouzon, Pfeiffer, Craniosynostosis, Apert, Jackson-Weiss, Beare-Stevenson cutis gyrata, Saethre-Chotzen, and syndromic craniosynostosis.
Multiple alternatively spliced transcript variants encoding different isoforms have been noted for this gene.


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

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