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Thermo Fisher Scientific Phospho-FGFR1 (Tyr766) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-FGFR1 (Tyr766) Polyclonal Antibody

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FGFR1 단백질의 Tyr766 인산화 부위를 인식하는 Rabbit Polyclonal Antibody. Western blot, IHC, ICC, ELISA 등 다양한 응용에 적합. Human, Mouse, Rat 반응성. 고순도 Protein A 정제, 안정적 액상 형태로 -20°C 보관.

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마지막 업데이트 2025. 08. 05. 오후 01:36
Thermo Fisher Scientific BS-3136R Phospho-FGFR1 (Tyr766) Polyclonal Antibody 100 ul pk판매 단위 pk ·
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569,000원VAT 포함 625,900원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-FGFR1 (Tyr766) Polyclonal Antibody

Thermo Fisher Scientific Phospho-FGFR1 (Tyr766) Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC-P) 1:200
Immunohistochemistry (Frozen) (IHC-F) 1:100–1:500
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1:500–1:1,000

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH-conjugated synthetic phosphopeptide derived from human FGFR1 around the phosphorylation site of Tyr766
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer 0.01M TBS, pH 7.4, with 50% glycerol, 1% BSA
Contains 0.02% ProClin 300
Storage Conditions -20°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

FGFR1 (also known as FLT2) is a member of the Fibroblast Growth Factor Receptor family, which includes four membrane-spanning tyrosine kinases (FGFR1–4). These receptors serve as high-affinity receptors for 17 growth factors (FGF1–17) and play crucial roles in mesoderm induction, cell growth, migration, organ formation, and bone growth.
FGFR1 undergoes alternative splicing, producing multiple variants expressed differently during embryonic development and in adult tissues. Mutations or defects in FGFR1 are associated with various diseases such as Pfeiffer syndrome, idiopathic hypogonadotropic hypogonadism, Kallmann syndrome type 2, osteoglophonic dysplasia, Jackson-Weiss syndrome, and Antley-Bixler syndrome.
Chromosomal aberrations involving FGFR1 are linked to stem cell myeloproliferative disorder and stem cell leukemia/lymphoma syndrome.

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

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