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antibody from antibodies-online
Targeting: FGFR2
BEK, CD332, CEK3, CFD1, ECT1, JWS, K-SAM, KGFR, TK14, TK25
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- Antibody Data
- Antigen structure
- References [4]
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- Validations
- Western blot [1]
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- Product number
- ABIN359857 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Fibroblast Growth Factor Receptor 2 (FGFR2) antibody
- Antibody type
- Polyclonal
- Description
- Prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS
- Reactivity
- Human
- Host
- Rabbit
- Vial size
- 0.4 mL
- Storage
- Store the antibody undiluted at 2-8°C for one month or (in aliquots) at-20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability.
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.
FGFR2 mutations in Pfeiffer syndrome.
McGillivray G, Savarirayan R, Cox TC, Stojkoski C, McNeil R, Bankier A, Bateman JF, Roscioli T, Gardner RJ, Lamandé SR
Journal of medical genetics 2005 Aug;42(8):656-62
Journal of medical genetics 2005 Aug;42(8):656-62
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability.
Park WJ, Meyers GA, Li X, Theda C, Day D, Orlow SJ, Jones MC, Jabs EW
Human molecular genetics 1995 Jul;4(7):1229-33
Human molecular genetics 1995 Jul;4(7):1229-33
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.
Rutland P, Pulleyn LJ, Reardon W, Baraitser M, Hayward R, Jones B, Malcolm S, Winter RM, Oldridge M, Slaney SF
Nature genetics 1995 Feb;9(2):173-6
Nature genetics 1995 Feb;9(2):173-6
FGFR2 mutations in Pfeiffer syndrome.
Lajeunie E, Ma HW, Bonaventure J, Munnich A, Le Merrer M, Renier D
Nature genetics 1995 Feb;9(2):108
Nature genetics 1995 Feb;9(2):108
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