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Thermo Fisher Scientific Phospho-FGFR1 (Tyr653, Tyr654) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-FGFR1 (Tyr653, Tyr654) Polyclonal Antibody

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FGFR1의 Tyr653 및 Tyr654 인산화 부위를 인식하는 Rabbit Polyclonal Antibody. Western blot, IHC, IP 등 다양한 응용 가능. 인간, 마우스, 랫트 반응성. 항원 친화 크로마토그래피로 정제된 액상 항체. 연구용으로만 사용.

카탈로그번호
441140G
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 02:48
Thermo Fisher Scientific 441140G Phospho-FGFR1 (Tyr653, Tyr654) Polyclonal Antibody 100 ul pk판매 단위 pk ·
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630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-FGFR1 (Tyr653, Tyr654) Polyclonal Antibody

Thermo Fisher Scientific Phospho-FGFR1 (Tyr653, Tyr654) Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 1:1,000 View 3 publications
Immunohistochemistry (IHC) - View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:10–1:100 -
Immunoprecipitation (IP) - View 1 publication

Product Specifications

Property Description
Species Reactivity Human, Mouse
Published Species Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen The antiserum was produced against a chemically synthesized phosphopeptide derived from the region of human FGFR that contains tyrosine 653 and 654. The sequence is conserved in human, mouse, and rat.
Conjugate Unconjugated
Form Liquid
Purification Antigen affinity chromatography
Storage Buffer Dulbecco’s PBS, pH 7.3, with 1 mg/mL BSA
Contains 0.05% sodium azide
Storage Conditions -20°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2533582

Target Information

FGFR1 (also known as FLT2) is a member of the Fibroblast Growth Factor Receptor family (FGFR1–4), which serve as high-affinity receptors for 17 growth factors (FGF1–17).
The FGF Receptor family plays a crucial role in biological processes such as mesoderm induction, patterning, cell growth, migration, organ formation, and bone growth.
FGFR1 undergoes alternative splicing, generating multiple variants that are differentially expressed during embryonic and adult stages.
Mutations or aberrations in FGFR1 are associated with several diseases, including Pfeiffer syndrome, idiopathic hypogonadotropic hypogonadism, Kallmann syndrome type 2, osteoglophonic dysplasia, non-syndromic trigonocephaly, Jackson-Weiss syndrome, and Antley-Bixler syndrome.
Chromosomal abnormalities 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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