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Thermo Fisher Scientific FGFR3 Monoclonal Antibody (1E3F9)
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Thermo Fisher Scientific FGFR3 Monoclonal Antibody (1E3F9)

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FGFR3 단백질을 인식하는 Mouse IgG2a 단일클론 항체로, Western blot, IHC, ICC, Flow cytometry, ELISA 등에 사용 가능. 인간 시료 반응성. 단백질 G로 정제된 액상 형태로 제공되며, 1 mg/mL 농도. 연구용으로만 사용.

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마지막 업데이트 2025. 07. 29. 오전 01:36
Thermo Fisher Scientific MA548457 FGFR3 Monoclonal Antibody (1E3F9) 100 ug pk판매 단위 pk ·
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717,500원VAT 포함 789,250원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR3 Monoclonal Antibody (1E3F9)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (IHC) 1:200–1:1,000
Immunocytochemistry (ICC/IF) 1:50–1:250
Flow Cytometry (Flow) 1:200–1:400
ELISA 1:10,000

Product Specifications

Property Description
Species Reactivity Human
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone 1E3F9
Immunogen Purified recombinant fragment of human FGFR3 (AA: 529–694) expressed in E. coli
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS
Contains 0.05% sodium azide
Storage Conditions Store at 4°C short term. For long-term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_3090768

Target Information

FGFR3 (Fibroblast Growth Factor Receptor 3) is a member of the FGFR family of receptor tyrosine kinases. This family regulates various cellular functions such as angiogenesis, mitogenesis, osteogenesis, myogenesis, carcinogenesis, differentiation, and tissue repair. FGFR family members differ in ligand affinity and tissue distribution and are implicated in diseases including cancer, rheumatoid arthritis, and diabetic retinopathy.

FGFR3 consists of:

  • An extracellular region with three immunoglobulin-like domains
  • A hydrophobic membrane-spanning segment
  • A cytoplasmic tyrosine kinase domain

The extracellular region interacts with fibroblast growth factors, triggering downstream signaling pathways that influence cell proliferation and differentiation. FGFR3 plays an essential role in bone development and maintenance. Mutations in FGFR3 are associated with craniosynostosis and various skeletal dysplasias. Three alternatively spliced transcript variants encoding distinct isoforms have been described.


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

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