LIN28 Antibody, Rabbit, Polyclonal

Catalog Number: NSJ-F41528-0.08ML
Article Name: LIN28 Antibody, Rabbit, Polyclonal
Biozol Catalog Number: NSJ-F41528-0.08ML
Supplier Catalog Number: F41528-0.08ML
Alternative Catalog Number: NSJ-F41528-0.08ML
Manufacturer: NSJ Bioreagents
Host: Rabbit
Category: Antikörper
Application: ELISA, FACS, WB
Species Reactivity: Human, Mouse
Immunogen: This LIN28A antibody was produced from rabbits immunized with a His fusion protein from human LIN28A.
Acts as a translational enhancer, driving specific mRNAs to polysomes and thus increasing the efficiency of protein synthesis. Its association with the translational machinery and target mRNAs results in an increased number of initiation events per molecule of mRNA and, indirectly, in stabilizing the mRNAs. Binds IGF2 mRNA, MYOD1 mRNA, ARBP/36B4 ribosomal protein mRNA and its own mRNA. Essential for skeletal muscle differentiation program through the translational up-regulation of IGF2 expression (By similarity). Acts as a suppressor of microRNA (miRNA) biogenesis by specifically binding the precursor let-7 (pre-let-7), a miRNA precursor. Acts by binding pre-let-7 and recruiting ZCCHC11/TUT4 uridylyltransferase, leading to the terminal uridylation of pre-let-7. Uridylated pre-let-7 miRNAs fail to be processed by Dicer and undergo degradation. Degradation of pre-let-7 in embryonic stem (ES) cells contributes to the maintenance of ES cells. In contrast, LIN28A down-regulation in neural stem cells by miR-125, allows the processing of pre-let-7. Specifically recognizes the 5-GGAG-3 motif in the terminal loop of pre-let-7. Also recognizes and binds non pre-let-7 pre-miRNAs that contain the 5-GGAG-3 motif in the terminal loop, leading to their terminal uridylation and subsequent degradation.
Clonality: Polyclonal
UniProt: Q9H9Z2
Purity: Purified
Form: In 1X PBS, pH 7.4, with 0.09% sodium azide
Antibody Type: Primary Antibody
Application Dilute: Western blot: 1:1000,Flow Cytometry: 1:10-1:50
Application Notes: Titration of the LIN28 antibody may be required due to differences in protocols and secondary/substrate sensitivity.