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Description
Images & Validation
−| Tested Applications | ELISA, WB |
|---|---|
| Dilution Range | ELISA: 1:5,000 - 1:25,000, WB: 1:500 - 1:3,000 |
| Reactivity | Human |
| Application Notes |
Key Properties
−| Antibody Type | Primary Antibody |
|---|---|
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Antiserum |
| Immunogen | Human NFKB2 p52/p100 peptide corresponding to aa residue 1-19 the human protein conjugated to Keyhole Limpet Hemocyanin (KLH). |
| Target | NFKB2 |
| Purity | This product was prepared from monospecific antiserum by delipidation and defibrination. Anti-Human NFKB2 p52 may react non-specifically with other proteins. Control peptide (orb343893) will compete only with the specific reaction of antiserum with Human NFKB2 p52. |
| Conjugation | Unconjugated |
Storage & Handling
−| Storage | Store vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use. |
|---|---|
| Form/Appearance | Liquid (sterile filtered) |
| Buffer/Preservatives | 0.01% (w/v) Sodium Azide |
| Concentration | 90 mg/mL |
| Expiration Date | 12 months from date of receipt. |
| Dry Ice Shipping | Please note: This product requires shipment on dry ice. A dry ice surcharge will apply. |
| Disclaimer | For research use only |
Alternative Names
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EMSA results using Anti-NFKB p52. Comparison of nuclear factor (NF)-κB binding activity among CD30-positive lymphomas with or without stimulation of CD30. (a) Whole-cell lysates of CD30-positive lymphoma cell lines with or without stimulation of CD30 were incubated with the 32P-labeled HIV κB probe, and κB binding was analyzed by electrophoretic mobility shift assay (EMSA). (b) Supershift assay of CD30-stimulated Karpas 299 and SR-786 using the antibodies indicated. Addition of anti-Bcl-3 antibodies produced no apparent supershifted bands (data not shown). The specificity of κB binding was determined by competition with an excess amount of unlabeled HIV κB probe or control unlabeled AP1 probe (5'-CGCTTGATGAGTCAGCCGGAA-3'). (c) NF-κB DNA-binding activities of p52-containing components were compared among CD30-positive lymphoma cell lines upon stimulation of CD30. The whole-cell lysates were incubated with the 32P-labeled H2 κB probe, and the binding was analyzed by EMSA. (d) Supershift assay of CD30-stimulated Karpas 299, KM-H2 and KIS-1. The cell lysates were first incubated with antibodies against p50, p52, p65, RelB and c-Rel, and the components of the NF-κB-binding complexes in each cell line were determined. The specificity of κB binding was determined by competition with an excess amount of unlabeled H2 κB probe or control unlabeled AP1 probe.

H1299 cells expressing mutant p53-R175H show increased binding to the NF-κB site. (A) Nuclear extracts of HC-5 and H-R175H were incubated as described in Materials and Methods with a 32P-labeled probe containing the sequence of the NF-κB DNA-binding site. Competition studies were done using a specific competitor (lanes 4 to 7) and a nonspecific competitor (lanes 8 to 11) at both 20× (lanes 4, 5, 8, and 9) and 40× (lanes 6, 7, 10, and 11) molar excess. The single arrows indicate the DNA complexes containing NF-κB complexes. Increased NF-κB activity is observed in the presence of mutant p53 (lanes 2, 3, and 8 to 11). The double arrow indicates the supershifted complex in the presence of antibodies specific for NF-κB1 (p50), NF-κB2 (p52), and p53 (lanes 12 to 15, 20 to 21, and 24 to 29, respectively). Equal amounts of protein were added to each lane.
Quick Database Links
UniProt Details
−NCBI Reference Sequences
−| Protein | NP_001070962.1 |
|---|
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Protocol Information
NFKB2 Antibody (orb750602)
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