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Thermo Fisher Scientific FGFR-1 Polyclonal Antibody
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Thermo Fisher Scientific FGFR-1 Polyclonal Antibody

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Rabbit polyclonal antibody targeting human FGFR-1 for IHC applications. High specificity and affinity purified by antigen chromatography. Suitable for research in cancer and developmental biology. Supplied in liquid form with stabilizer for reliable st...

카탈로그번호
500-10584
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 06:51
Thermo Fisher Scientific 500-10584 FGFR-1 Polyclonal Antibody 100 ug pk판매 단위 pk ·
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421,400원VAT 포함 463,540원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR-1 Polyclonal Antibody

Applications

  • Immunohistochemistry (Paraffin) (IHC (P))

Tested Dilution: 2–10 µg/mL
Publications: [References available upon request]


Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from internal sequence of human FGFR-1 protein
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with proprietary stabilizer
Contains 0.01% 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)

Product Specific Information

  • Positive control: Breast carcinoma
  • Cellular location: Cytoplasmic, membrane

Target Information

FGFR1 (also known as FLT2) is a member of the Fibroblast Growth Factor Receptor family (FGFR1–4), which are high-affinity receptors for 17 growth factors (FGF1–17). These receptors play key roles in mesoderm induction, patterning, cell growth and migration, organ formation, and bone development.
FGFR1 undergoes alternative splicing, generating multiple variants expressed during embryonic and adult stages. Mutations or defects in FGFR1 are associated with several disorders, including Pfeiffer syndrome, idiopathic hypogonadotropic hypogonadism (IHH), Kallmann syndrome type 2 (KAL2), osteoglophonic dysplasia (OGD), non-syndromic trigonocephaly, Jackson-Weiss syndrome, and Antley-Bixler syndrome.
Chromosomal aberrations involving FGFR1 have been linked to stem cell myeloproliferative disorder and stem cell leukemia lymphoma syndrome.


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

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