FGFR2 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA131990-Each-of-1 | In Stock | ₹ 57,672.00 |
PIPA131990 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 57,672.00
GST (18%): ₹ 10,380.96
Total Price: ₹ 68,052.96
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
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
14183, 2263
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Flow Cytometry, Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
0.5 mg/mL
Formulation
PBS with 0.09% sodium azide
Gene Accession No.
P21802, P21803
Gene Symbols
FGFR2
Immunogen
KLH conjugated synthetic peptide between 22-51 amino acids from the N-terminal region of human FGFR2.
Quantity
400 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Positive Control: Jurkat cell lysate Store as concentrated solution
- Centrifuge briefly prior to opening vial
- 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.