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

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Rabbit polyclonal antibody against human FGFR2 for IHC (paraffin) applications. Recognizes internal peptide region of FGFR-2. Recommended antigen retrieval with citrate buffer pH 6.0. Suitable positive controls: liver or breast carcinoma.

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pk
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마지막 업데이트 2025. 08. 05. 오후 10:44
Thermo Fisher Scientific PA137685 FGFR2 Polyclonal Antibody 1 mL pk판매 단위 pk ·
재고 확인 필요
1,000,500원VAT 포함 1,100,550원
Thermo Fisher Scientific PA532404 FGFR2 Polyclonal Antibody 500 ul pk판매 단위 pk ·
재고 확인 필요
698,100원VAT 포함 767,910원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR2 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC (P)) 1:100

Product Specifications

항목 내용
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide from internal region of human FGFR-2 protein
Conjugate Unconjugated
Form Liquid
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_1074390

Product Specific Information

Heat-mediated antigen retrieval is recommended prior to staining, using a 10 mM citrate buffer (pH 6.0) for 10 minutes, followed by cooling at room temperature for 20 minutes.
After antigen retrieval, incubate samples with primary antibody for 10 minutes at room temperature.
Suggested positive controls: liver or breast carcinoma.

Target Information

FGFR2 (Fibroblast Growth Factor Receptor 2) belongs to the FGFR family of receptor tyrosine kinases, which regulate various cellular functions such as angiogenesis, mitogenesis, osteogenesis, myogenesis, carcinogenesis, cellular differentiation, and tissue repair.
FGFR family members are implicated in diseases including cancer, rheumatoid arthritis, and diabetic retinopathy.
Mutations in FGFR2 are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis.
Multiple alternatively spliced transcript variants encoding different isoforms have been identified.


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

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