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Thermo Fisher Scientific FGFR1 Polyclonal Antibody
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Thermo Fisher Scientific FGFR1 Polyclonal Antibody

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FGFR1 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, Human 및 Mouse 시료에 반응합니다. Western blot, IHC, Flow Cytometry 등 다양한 응용에 적합하며, 고순도 및 안정적인 액상 형태로 제공됩니다.

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마지막 업데이트 2025. 08. 04. 오전 10:31
Thermo Fisher Scientific PA525979 FGFR1 Polyclonal Antibody 400 ul pk판매 단위 pk ·
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699,000원VAT 포함 768,900원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR1 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 1:1,000 -
Immunohistochemistry (IHC) - View 2 publications
Immunohistochemistry (Paraffin) (IHC (P)) 1:10–1:50 -
Flow Cytometry (Flow) 1:10–1:50 -
in situ PLA (PLA) - View 1 publication

Product Specifications

Specification Description
Species Reactivity Human, Mouse
Published Species Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen His fusion protein from human N-terminal FGFR1
Conjugate Unconjugated
Form Liquid
Concentration 2 mg/mL
Purification Ammonium sulfate precipitation, size-exclusion, dialysis
Storage Buffer PBS, pH 7.4
Contains 0.09% sodium azide
Storage Conditions Store at 4°C short term; for long term, store at -20°C avoiding freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2543479

Target Information

FGFR1 (also known as FLT2) is a member of the Fibroblast Growth Factor Receptor family, consisting of four membrane-spanning tyrosine kinases (FGFR1–4) that serve as high-affinity receptors for 17 growth factors (FGF1–17).
The FGF receptor family plays a key role in biological processes such as mesoderm induction, cell growth and migration, organ formation, and bone development.
FGFR1 undergoes alternative splicing, generating multiple variants expressed differently during embryonic and adult stages.
Defects in FGFR1 are associated with several disorders including Pfeiffer syndrome, idiopathic hypogonadotropic hypogonadism, Kallmann syndrome type 2, osteoglophonic dysplasia, and others.
Chromosomal aberrations involving FGFR1 can lead 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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