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Catalog Number | orb758942 |
---|---|
Category | Antibodies |
Description | Hamster monoclonal antibody to CD79b |
Target | CD79b |
Clonality | Monoclonal |
Species/Host | Hamster |
Isotype | IgG |
Conjugation | Unconjugated |
Reactivity | Mouse |
Concentration | 1 mg/ml |
Buffer/Preservatives | PBS with 0.02% Proclin 300. |
Purity | Purified |
Immunogen | HM79-16 was initially generated by purifying CD79b from WEHI231 B cells and used for immunisation of footpads of an Armenian hamster. Hybridoma supernatants were screened for positive reactivity in surface immunofluorescence of WEHI231 and then the specificity to CD79b was tested by immuno-precipitationRecombinant anti-CD79 antibodies were engineered by cloning and sequencing the full-length IG heavy and light chains of an Armenian hamster (Cricetulus migratorius). |
UniProt ID | P15530 |
Tested applications | FC, IF, IHC, IP |
Clone Number | HM79-16 |
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. |
Alternative names | Ig-beta; AGM6; B29; IGB; CD79b molecule; |
Note | For research use only |
Flow cytometry using the Anti-CD79b antibody HM79-16. Paraformaldehyde fixed mouse splenocytes were stained with anti-unknown specificity antibody (orb256458; isotype control, black line) or the rabbit IgG version of HM79-16 (orb758943, 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 fixed mouse splenocytes with anti-CD79b antibody HM79-16. Immunofluorescence analysis of paraformaldehyde fixed mouse splenocytes on Shi-fix™ coverslips stained with the chimeric rabbit IgG version HM79-16 (orb758943) at 10 µg/ml for 1h followed by Alexa Fluor® 488 secondary antibody (2 µg/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom orb758943, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody (orb256449) followed by staining with Alexa Fluor® 488 secondary antibody.
Western Blot using anti-CD79b antibody HM79-16 Mouse spleen tissue lysates (35 µg protein in RIPA buffer) were resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of HM79-16 (orb758943) at 0.1 µg/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.