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FGF17 Antibody (500-P152BT-1MG) in WB
Western Blot: To detect hFGF-17 by Western Blot analysis FGF17 Polyclonal Antibody, Biotin (Product # 500-P152BT-1MG) can be used at a concentration of 0.1-0.2 µg/mL. Used in conjunction with compatible secondary reagents the detection limit for Recombinant hFGF-17 is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions.
Product Details
500-P152BT-1MG
Applications
Tested Dilution
Publications
Product Specifications
Host/Isotype
Rabbit
Class
Polyclonal
Type
Antibody
Immunogen
E.coli-derived Recombinant Human FGF-17
Conjugate
Form
Lyophilized
Concentration
0.1-1.0 mg/mL
Storage conditions
-20°C
Shipping conditions
Ambient
RRID
AB_2929500
Product Specific Information
AA Sequence of recombinant protein: MTQGENHPSP NFNQYVRDQG AMTDQLSRRQ IREYQLYSRT SGKHVQVTGR RISATAEDGN KFAKLIVETD TFGSRVRIKG AESEKYICMN KRGKLIGKPS GKSKDCVFTE IVLENNYTAF QNARHEGWFM AFTRQGRPRQ ASRSRQNQRE AHFIKRLYQG QLPFPNHAEK QKQFEFVGSA PTRRTKRTRR PQPLT.
Preparation: Produced from sera of rabbits immunized with highly pure Recombinant Human FGF-17. Anti-Human FGF-17-specific antibody was purified by affinity chromatography and then biotinylated.
Direct ELISA: To detect Human FGF-17 by direct ELISA (using 100 µL/well) a concentration of approximately 1.0 µg/mL of this antibody is required. This biotinylated polyclonal antibody allows the detection of at least 2000-4000 pg/mL of Recombinant Human FGF-17.
Western Blot: To detect hFGF-17 by Western Blot analysis this antibody can be used at a concentration of 0.1-0.2 µg/mL. Used in conjunction with compatible secondary reagents the detection limit for Recombinant hFGF-17 is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions.
500-P152BT-1 mg will be provided as 2 x 500 µg
Target Information
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was shown to be prominently expressed in the cerebellum and cortex. The mouse homolog of this gene was localized to specific sites in the midline structures of the forebrain, the midbrain-hindbrain junction, developing skeleton and developing arteries, which suggests a role in central nervous system, bone and vascular development. This gene was referred to as FGF-13 in reference 2, however, its amino acid sequence and chromosomal localization are identical to FGF17.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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