Human FGF12 Matched Antibody Pair Set [ABP-Q-0632] (CAT#: ABP-Q-0632)

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Human FGF12 Matched Antibody Pair set for ELISA useCapture Antibody: Rabbit purified polyclonal anti-FGF12Detection Antibody: Mouse monoclonal anti-FGF12, IgG1 Kappa

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Antigen Detail

TargetFGF12
DescriptionFibroblast growth factor 12 is a protein that in humans is encoded by the FGF12 gene. FGF12 regulates the BMP (bone morphogenic protein)-induced human pulmonary arterial smooth muscle cell phenotype change. FGF12 exerts antiproliferative and prodifferentiation effects in human pulmonary arterial smooth muscle cells via p38MAPK-dependent MEF2a (myocyte enhancer factor 2a) pathway activation.
Species ReactivityHuman

Capture Antibody

Capture ClonalityPolyclonal
Host SpeciesRabbit
PurificationAffinity chromatography
BufferPBS, pH 7.4, containing 0.1% Proclin 300
ApplicationELISA

Detection Antibody

Det-ClonalityMonoclonal
Host SpeciesMouse
ConjugationUnconjugated
CloneRD10104
IsotypeIgG1, kappa
PurificationAffinity chromatography
BufferPBS, pH 7.4

General Product Property

Product OverviewHuman FGF12 Matched Antibody Pair set for ELISA use
Capture Antibody: Rabbit purified polyclonal anti-FGF12
Detection Antibody: Mouse monoclonal anti-FGF12, IgG1 Kappa
SpecificityValidated for detecting natural and recombinant human FGF12
Research AreaAngiogenesis
ApplicationELISA
Application NotesOptimal dilutions should be determined experimentally by the user.
FormLyophilized
StorageAvoid repeated freeze/thaw cycles. Store at 2-8°C for short term. Aliquot and store at -20°C for long term storage.
Size1 Set
Sample TypeSerum; Supernatant; Urine; Cell lysate; Plasma; Tissue Homogenates
Usage StatementAvailable for Research Use Only. Not for use in therapeutic or diagnostic applications.

Target Overview

Gene SymbolFGF12
Full NameFibroblast Growth Factor 12
BackgroundThe protein encoded by this gene is a member of the fibroblast growth factor 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 growth factor lacks the N-terminal signal sequence present in most of the FGF family members, but it contains clusters of basic residues that have been demonstrated to act as a nuclear localization signal. When transfected into mammalian cells, this protein accumulated in the nucleus, but was not secreted. The specific function of this gene has not yet been determined. Two alternatively spliced transcript variants encoding distinct isoforms have been reported.
Alternative NamesFHF1; EIEE47
Gene ID2257
Uniprot IDP61328
GeneCardsFGF12
HGNC3668
EnsemblENSG00000114279
OMIM601513
Involvement in DiseaseDiseases associated with FGF12 include Epileptic Encephalopathy, Early Infantile, 47 and Undetermined Early-Onset Epileptic Encephalopathy.
FunctionInvolved in nervous system development and function. Involved in the positive regulation of voltage-gated sodium channel activity. Promotes neuronal excitability by elevating the voltage dependence of neuronal sodium channel SCN8A fast inactivation.
Related PathwaysIts related pathways are NF-KappaB Family Pathway and Activation of cAMP-Dependent PKA.

For Research Use Only.

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