Human Fibroblast Growth Factor Receptor 4 (FGFR4) Enzyme

Este producto es parte de FGFR4 - fibroblast growth factor receptor 4
Human Fibroblast Growth Factor Receptor 4 (FGFR4) Enzyme
234€ (2 µg)

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Name
Human Fibroblast Growth Factor Receptor 4 (FGFR4) Enzyme
Category
Proteins and Peptides
Provider
Abbexa
Reference
abx073881
Tested Applications
SDS-PAGE

Description

Fibroblast Growth Factor Receptor-4 Protein is a recombinant protein kinase.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Proteins and Peptides
Immunogen Target
Fibroblast Growth Factor Receptor 4 (FGFR4)
Host
Insect
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Origin
Human
Expression
Recombinant
Purity
> 90% (SDS-PAGE and RP-HPLC)
Size 1
2 µg
Size 2
10 µg
Size 3
1 mg
Form
Lyophilized
Tested Applications
SDS-PAGE
Availability
Shipped within 5-10 working days.
Dry Ice
No
UniProt ID
P22455
Alias
TKF,JTK2,CD334,FGFR-4
Background
Protein FGFR4
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Background

Fibroblast growth factor receptor 4 (FGFR4) FGFR4 is a member of the fibroblast growth factor receptor (FGFR) family, characterized as a transmembrane tyrosine kinase receptor that binds FGFs to regulate cell proliferation, differentiation, migration, and survival. Structurally, FGFR4 consists of an extracellular ligand-binding domain composed of three immunoglobulin-like loops, a single transmembrane domain, and an intracellular tyrosine kinase domain. FGFR4 plays essential roles in embryonic development, metabolism, and tissue homeostasis, particularly in liver, muscle, and endocrine tissues. Ligand binding activates downstream signaling cascades, including the MAPK, PI3K-AKT, and STAT pathways, which are critical for cell growth and survival. Dysregulation of FGFR4 signaling has been implicated in various cancers, such as hepatocellular carcinoma and rhabdomyosarcoma, where overexpression or mutation drives tumor growth and metastasis. Its selective expression in specific tissues and its involvement in metabolic regulation, including bile acid synthesis, highlight its specialized biological functions and potential as a therapeutic target in oncology and metabolic disorders.

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