Reactivity: | Human, Mouse, Rat |
Applications: | WB, IP, ELISA |
Host Species: | Rabbit |
Isotype: | IgG |
Clonality: | Monoclonal antibody |
Gene Name: | CUGBP Elav-like family member 1 |
Gene Symbol: | CELF1 |
Synonyms: | CUGBP; NAB50; NAPOR; CUG-BP; CUGBP1; hNab50; BRUNOL2; EDEN-BP; CELF1 |
Gene ID: | 10658 |
UniProt ID: | Q92879 |
Clone ID: | 2B2P2 |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 1-100 of human CELF1 (Q92879). |
Dilution: | WB 1:500-1:2000 |
Purification Method: | Affinity purification |
Concentration: | 0.40 mg/ml |
Buffer: | PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3. |
Storage: | Store at -20°C. Avoid freeze/thaw cycles. |
Documents: | Manual-CELF1 antibody |
Background
Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. This gene may play a role in myotonic dystrophy type 1 (DM1) via interactions with the dystrophia myotonica-protein kinase (DMPK) gene. Alternative splicing results in multiple transcript variants encoding different isoforms.
Images
![]() | Western blot analysis of lysates from SH-SY5Y cells, using CELF1 Rabbit mAb (A1150) at 1:1000 dilution. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution. Lysates/proteins: 25μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 1s. |
![]() | Western blot analysis of various lysates, using CELF1 Rabbit mAb (A1150) at 1:1000 dilution. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution. Lysates/proteins: 25μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 3s. |
![]() | Immunoprecipitation of CELF1 from 200 µg extracts of SH-SY5Y cells was performed using 0.5 µg of CELF1 Rabbit mAb (A1150). Rabbit IgG isotype control(AC042) was used to precipitate the Control IgG sample. IP samples were eluted with 1X Laemmli Buffer. The Input lane represents 10% of the total input. Western blot analysis of immunoprecipitates was conducted using CELF1 Rabbit mAb (A1150) at a dilution of 1:1000. |
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