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Catalog Number | orb1089986 |
---|---|
Category | Antibodies |
Description | Rabbit monoclonal antibody to RRM2 |
Species/Host | Rabbit |
Clonality | Monoclonal |
Clone Number | SAIC-30C-18 |
Tested applications | ELISA, WB |
Reactivity | Human |
Isotype | IgG |
Immunogen | The KLH-conjugated peptide "IEQEFLTEALPVK" derived from Ribonucleoside-diphosphate reductase subunit M2 (RRM2). RRM2 provides precursors required for DNA synthesis. |
Concentration | 1 mg/ml |
Purity | Purified |
Conjugation | Unconjugated |
Target | RRM2 |
UniProt ID | P31350 |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Buffer/Preservatives | PBS with 0.02% Proclin 300. |
Alternative names | RR2; R2; RR2M; ribonucleotide reductase regulatory Read more... |
Note | For research use only |
Expiration Date | 12 months from date of receipt. |
Flow cytometry using the Anti-RRM2 antibody SAIC-30C-18. Paraformaldehyde fixed HeLa cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (orb256458; isotype control, black line) or the rabbit IgG version of SAIC-30C-18 (orb1089986, blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor® 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.
Immunofluorescence staining of HeLa cells with anti-RRM2 SAIC-30C-18. Immunofluorescence analysis of paraformaldehyde fixed HeLa cells permeabilized with 0.15% Triton stained with the chimeric rabbit IgG version of SAIC-30C-18 (orb1089986) (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom orb1089986, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody (orb256458) followed by staining with Alexa Fluor® 488 secondary antibody.
Western Blot using anti-RRM2 antibody SAIC-30C-18. Jurkat cell lysates (35 µg protein in RIPA buffer) were resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of SAIC-30C-18 (orb1089986) at 1 µg/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.