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anti-Human FGF17 Antikörper:
anti-Mouse (Murine) FGF17 Antikörper:
anti-Rat (Rattus) FGF17 Antikörper:
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Human Polyclonal FGF17 Primary Antibody für ICC, IF - ABIN4311578
Puranam, He, Yao, Le, Jang, Rehder, Lewis, McNamara: Disruption of Fgf13 causes synaptic excitatory-inhibitory imbalance and genetic epilepsy and febrile seizures plus. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2015
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.
fibroblast growth factor 17
, fibroblast growth factor 17 b
, fibroblast growth factor 17b