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Thermo Fisher Scientific Phospho-FGFR1 (Tyr307) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-FGFR1 (Tyr307) Polyclonal Antibody

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Rabbit polyclonal antibody recognizing phospho-FGFR1 (Tyr307). Validated for dot blot. Predicted cross-reactivity with chicken and mouse. Suitable for research on FGFR1 signaling and related pathways.

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마지막 업데이트 2025. 08. 04. 오전 03:24
Thermo Fisher Scientific PA512745 Phospho-FGFR1 (Tyr307) Polyclonal Antibody 400 ul pk판매 단위 pk ·
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660,800원VAT 포함 726,880원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-FGFR1 (Tyr307) Polyclonal Antibody

Applications

  • Dot blot (DB): 1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH-conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding Y307 of human FGFR1
Conjugate Unconjugated
Form Liquid
Purification Protein A, Antigen affinity chromatography
Storage buffer PBS, pH 7.4
Contains 0.09% 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_10981105

Product Specific Information

This antibody is predicted to react with chicken and mouse based on sequence homology.

Target Information

FGFR1 (also known as FLT2) is a member of the Fibroblast Growth Factor Receptor family (FGFR1–4), which are membrane-spanning tyrosine kinases serving 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, cell growth, migration, organ formation, and bone development.
FGFR1 undergoes alternative splicing, generating multiple variants expressed differently during embryonic and adult stages.
Mutations or aberrations in FGFR1 are associated with several diseases, including:

  • Pfeiffer syndrome (PS)
  • Idiopathic hypogonadotropic hypogonadism (IHH)
  • Kallmann syndrome type 2 (KAL2)
  • Osteoglophonic dysplasia (OGD)
  • Non-syndromic trigonocephaly
  • Jackson-Weiss syndrome
  • 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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