FGFR2 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA596049-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA596049 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
FGFR2
Classification
Polyclonal
Conjugate
Unconjugated
Gene
FGFR2
Gene Alias
AU043015, AW556123, bacteria-expressed kinase, BBDS, BEK, BEK fibroblast growth factor receptor, BFR-1, CD332, CEK3, CFD1, ECT1, FGF Receptor 2, FGF-10, FGFR2, FGFR-2, Fgfr7, Fgfr-7, fibroblast growth factor receptor 2, JWS, Keratinocyte growth factor receptor, KGFR, KGFRTr, KSAM, K-SAM, protein tyrosine kinase, receptor like 14, Soluble KGFR, svs, TK14, TK25
Host Species
Rabbit
Purification Method
Affinity Chromatography
Regulatory Status
RUO
Gene ID (Entrez)
14183, 2263, 25022
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Applications
Immunohistochemistry (Paraffin)
Concentration
0.39 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide, pH 7.3
Gene Accession No.
P21802, P21803
Gene Symbols
FGFR2
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 1-100 of human FGFR2 (NP_0001323)
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Positive Samples: 293T, LO2; Cellular Location: Cell membrane, Cytoplasmic vesicle, Golgi apparatus, Single-pass type I membrane protein Immunogen sequence: MVSWGRFICL VVVTMATLSL ARPSFSLVED TTLEPEEPPT KYQISQPEVY VAAPGESLEV RCLLKDAAVI SWTKDGVHLG PNNRTVLIGE YLQIKGATPR FGFR2 is a member of the FGFR family of receptor tyrosine kinases
- This family is known to regulate a host of cellular functions including angiogenesis, mitogenesis, osteogenesis, myogenesis, carcinogenesis, cellular differentiation, and tissue repair after injury
- The FGFR family has also been implicated in a number of diseases including cancer, rheumatoid arthritis, and diabetic retinopathy
- FGFR family members differ from one another in their ligand affinities and tissue distribution
- Mutations in this gene are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis
- Multiple alternatively spliced transcript variants encoding different isoforms have been noted for this gene.