Rat Fibroblast Growth Factor Receptor 4 (FGFR4) Protein (Active)

Este producto es parte de FGFR4 - fibroblast growth factor receptor 4
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1079€ (100 µg)

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935106861
info@markelab.com
name
Rat Fibroblast Growth Factor Receptor 4 (FGFR4) Protein (Active)
category
Proteins and Peptides
provider
Abbexa
reference
abx691213
tested applications
SDS-PAGE

Description

Rat FGFR4 Protein is a recombinant protein from Rat produced in HEK293 Cells. A DNA sequence encoding the rat FGFR4 (Q498D6) extracellular domain (Met 1-Asp 367) was fused with the Fc region of human IgG1 at the C-terminus.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Proteins and Peptides
Immunogen Target
FGFR4
Host
HEK293 cells
Origin
Rat
Observed MW
Molecular Weight: 66 kDa
Sequence Fragment: Met1-Asp367
Tag: C-terminal Fc tag
Validity: The validity for this protein is 12 months.
Expression
Recombinant
Purity
> 90% (SDS-PAGE)
Size 1
100 µg
Form
 
Tested Applications
SDS-PAGE
Buffer
Lyophilized from sterile PBS, pH 7.4.
Availability
Shipped within 5-15 working days.
Storage
Aliquot and store at -20°C or -80°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q498D6
Alias
TKF,JTK2,CD334,FGFR-4
Background
Protein FGFR4
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

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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