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The protein encoded by HSP27 is induced by environmental stress and developmental changes. Additionally we are shipping and and many more products for this protein.
Showing 10 out of 38 products:
placental HSP 27 may play a role in labor and is spatially controlled
We propose that Atg7 (show ATG7 ELISA Kits) acts downstream of Hsp27 in the regulation of eye morphology, polyglutamine toxicity, and lifespan in Drosophila.
The data suggest that the Drosophila HSP27 protein acts as a chaperone to provide cellular stress resistance, although its function may be limited to a subset of the stress response such as the starvation resistance.
study identifies two distinct sets of sequences respectively mediating the nuclear import of Hsp27 and its association to nuclear speckles.
The functional similarities and differences of neuronal expression of hsp26 and hsp27 in adult Drosophila were demonstrated.
Loss of HspB1 (show HSPB1 ELISA Kits) specifically reduces myofibril size in embryonic craniofacial muscles.
Results show the sequence, expression, regulation, and function of a zebrafish protein (zfHsp27) and define zebrafish as a new model for the study of Hsp27 (show HSPB1 ELISA Kits) function.
initial upregulation of hsp27 (show HSPB1 ELISA Kits) expression occurs during early gastrulation
hspb1 (show HSPB1 ELISA Kits) is expressed during development
Hsp27 (show HSPB1 ELISA Kits) is dispensable for zebrafish morphogenesis but could play a role in long-term maintenance of heart and muscle tissues.
The data support a mechanism of Hsp27 (show HSPB1 ELISA Kits) function where interactions with the titin (show TTN ELISA Kits) filament system protect myofibrils from stress-induced degradation.
Xenopus HSP27 (show HSPB1 ELISA Kits), like HSP30, is a developmentally-regulated heat-inducible molecular chaperone (show HSP90AA1 ELISA Kits).
The protein encoded by this gene is induced by environmental stress and developmental changes. The encoded protein is involved in stress resistance and actin organization and translocates from the cytoplasm to the nucleus upon stress induction. Defects in this gene are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN).
, Hsp 27
, heat shock protein 237
, heat shock protein 27
, heat shock protein hsp27
, protein 27
, 25 kDa heat shock protein
, heat shock 27kDa protein 1
, heat shock protein beta-1