ACCÈS RAPIDE AUX LIENS
In humans, the RecQ helicase family includes WRN, BLM, RecQL1, RecQL4 and RecQL5 proteins, all of which contain a conserved helicase domain. WRN and BLM have been demonstrated to be the responsible genes in Werner and Bloom syndromes, respectively. RecQL1 and RecQL5 also belong to the human RecQ helicase family, but their correlation with genetic disorders, if any, is unknown. The levels of RecQ helicase family members are differentially upregulated to guarantee genomic stability in cells that are transformed or actively proliferating. The gene encoding human RecQL4, which maps to chromosome 8q24.3, is believed to be the gene responsible for the development of Rothmund-Thomson syndrome (RTS). The genes encoding RecQL1 and RecQL5 map to chromosome 12p12.1 and 17q25.1, respectively.
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Informations pour la commande
Nom du produit | Ref. Catalogue | COND. | Prix HT | QTÉ | Favoris | |
Anticorps RecQL1 (C-5) | sc-271437 | 200 µg/ml | $316.00 | |||
RecQL1 (C-5): m-IgGκ BP-HRP Kit | sc-534962 | 200 µg Ab; 40 µg BP | $354.00 | |||
RecQL1 (C-5): m-IgG2a BP-HRP Kit | sc-546203 | 200 µg Ab; 10 µg BP | $354.00 | |||
RecQL1 (C-5) peptide neutralisant | sc-271437 P | 100 µg/0.5 ml | $68.00 |