Item no. |
PRS-15-021-100uL |
Manufacturer |
ProSci
|
Amount |
100 uL |
Quantity options |
100 uL
|
Format |
Liquid |
Applications |
IF, IHC |
Specific against |
Human (Homo sapiens) |
Host |
Rabbit |
Isotype |
IgG |
Conjugate/Tag |
Unconjugated |
NCBI |
FGFR1 |
Alias |
FGFR1, soluble FGFR1 variant 2, soluble FGFR1 variant 1, proto-oncogene c-Fgr, OTTHUMP00000190880, OTTHUMP00000190876, OTTHUMP00000190875, OGD, N-SAM, KAL2, hydroxyaryl-protein kinase, heparin-binding growth factor receptor, HBGFR, fms-related tyrosine kinase 2, FMS-like tyrosine kinase 2, FLT-2, FLT2, FLJ99988, FLG, fibroblast growth factor receptor 1, FGFR-1, FGFBR, CEK, CD331, bFGF-R-1, BFGFR, basic fibroblast growth factor receptor 1 |
Available |
|
Specificity |
Human |
Shipping Temperature |
Blue Ice |
Storage Conditions |
Store at -20°C. Avoid freeze / thaw cycles. |
Manufacturer - Research Area |
Cancer, Cell Cycle, Growth Factors, Immunology, Neuroscience, Signal Transduction |
Background |
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. |
Purification |
Affinity purification |
Concentration |
Batch dependent |
Buffer |
PBS with 0.02% sodium azide, 50% glycerol, pH 7.3 |
Immunogen |
Recombinant fusion protein containing a sequence corresponding to amino acids 22-290 of human FGFR1 (NP_075598.2). |
Clonality |
Polyclonal |
NCBI Organism |
Homo sapiens |
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