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Recombinant Human FGFR2IIIc Protein

CAT: 0013-GTR19124031-01Size: 10 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR19124031-01Size:10 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Recombinant Human Fibroblast growth factor receptor 2 (IIIc) is produced by our Mammalian expression system and the target gene encoding Arg22-Glu377 is expressed with a human IgG1 Fc tag at the C-terminus.
Product Name Alternative
BEK, FGFR2IIIc; CD332; FGF R2b; FGFR2 beta; FGFR2; FGFR2b
UniProt
P21802
Expression Region
Arg22-Glu377
Conjugation
Unconjugated
Tag
C-Fc
Origin
Human
Endotoxin
< 1 EU/μg as determined by LAL test.
Purity
SDS-PAGE: Greater than 95% as determined by reducing SDS-PAGE.. SEC-HPLC: Greater than 95% as determined by SEC-HPLC. (QC verified)
Form
Lyophilized
Molecular Weight
Predicted: 66.5 KDa. Observed: 85-120 KDa, reducing conditions
Storage Conditions
Lyophilized protein should be stored at ≤ -20°C, stable for one year after receipt. Reconstituted protein solution can be stored at 2-8°C for 2-7 days. Aliquots of reconstituted samples are stable at ≤ -20°C for 3 months.
Notes
For research use only.
Preservative
0.2 μm filtered solution of PBS, pH 7.4.

UniProtKB · P21802

Fibroblast growth factor receptor 2

FGFR2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P21802
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
FGFR2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
FGFR-2
EC number
2.7.10.1
Processing
Precursor
Secondary accessions
B4DFC2, E7EVR6, E9PCR0, P18443, Q01742, Q12922, Q14300, Q14301, Q14302, Q14303, Q14304, Q14305, Q14672, Q14718, Q14719, Q1KHY5, Q86YI4, Q8IXC7, Q96KL9, Q96KM0, Q96KM1, Q96KM2, Q9NZU2, Q9NZU3, Q9UD01, Q9UD02, Q9UIH3, Q9UIH4, Q9UIH5, Q9UIH6, Q9UIH7, Q9UIH8, Q9UM87, Q9UMC6, Q9UNS7, Q9UQH7, Q9UQH8, Q9UQH9, Q9UQI0
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Biological process

Apoptosis

Ligand

ATP-bindingNucleotide-binding

Cellular component

Cell membraneCytoplasmic vesicleGolgi apparatusMembraneSecreted

Disease

CraniosynostosisDisease variantEctodermal dysplasiaIntellectual disabilityLacrimo-auriculo-dento-digital syndromeProto-oncogene

PTM

Disulfide bondGlycoproteinPhosphoproteinUbl conjugation

Molecular function

Heparin-bindingKinaseReceptorTransferaseTyrosine-protein kinase

Domain

Immunoglobulin domainRepeatSignalTransmembraneTransmembrane helix

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