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Abnova™ Human FGFR1 (NM_000604.2, 456 a.a. - 765 a.a.) V561M mutant Partial Protein expressed in Sf9 cells

Used for Func, SDS-PAGE

Supplier:  Abnova™ P4832

Catalog No. 89-944-513


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Description

Description

The protein encoded by this gene is a member of the fibroblast growth factor receptor (FGFR) family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member binds both acidic and basic fibroblast growth factors and is involved in limb induction. Mutations in this gene have been associated with Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, and autosomal dominant Kallmann syndrome 2. Chromosomal aberrations involving this gene are associated with stem cell myeloproliferative disorder and stem cell leukemia lymphoma syndrome. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq]

Specifications

Specifications

NM_000604.2
Functional Study, SDS-PAGE
2260
FGFR1 (V561M) (Human) Recombinant Protein
GST affinity chromatography
100 ug
RUO
FGFR1
75pmol/μg x min
None
Liquid
0.140 ug/uL
Liquid
35,899kDa
Insect cell (Sf9) expression system
2 ug/lane SDS-PAGE Stained with Coomassie Blue
Store at -80°C. Aliquot to avoid repeated freezing and thawing
BFGFR/CD331/CEK/FGFBR/FLG/FLJ99988/FLT2/HBGFR/KAL2/N-SAM
FGFR1
Baculovirus
Insect cell (Sf9) expression system
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