Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Conjugation:
Unconjugated
Alternative Names:
B29, Igb, Igbeta, Ig-beta
The B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-beta protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described.
WB,1:1000 - 1:4000|IF/ICC,1:200 - 1:2000|IF-P,1:200 - 1:2000|FC,1:500 - 1:1000|ELISA,Recommended starting concentration is 1 µg/mL. Please optimize the concentration based on your specific assay requirements.
Western blot analysis of lysates from Mouse spleen usingCD79b Rabbit mAb (A25358) at1:1000 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: 30s.
Confocal imaging of A20 cells usingCD79b Rabbit mAb (A25358, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 100x.
Confocal imaging ofparaffin-embedded Mouse spleen usingCD79b Rabbit mAb (A25358, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 40x. Perform high pressure antigen retrieval with 0.01 M citrate buffer (pH 6.0) prior to IF staining.
Confocal imaging ofparaffin-embedded Mouse thymus usingCD79b Rabbit mAb (A25358, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 40x. Perform high pressure antigen retrieval with 0.01 M citrate buffer (pH 6.0) prior to IF staining.
Flow cytometry: 1X10 6 C2C12 cells (negative control,left)and A20 (right) cells were surface-stained with Mouse CD79b mAb (A25358,2 µg/mL,orange line) or PE Rabbit IgG isotype control (A24172,5 µl/Test,blue line), followed by PE conjugated Donkey anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).
Flow cytometry: 1X10 6 A20 cells were surface-stained with PE Rabbit IgG isotype control (A24172,5 µl/Test,left) or Mouse CD79b mAb (A25358,2 µg/mL,right).
Flow cytometry: 1X10 6 C57BL/6 mouse Splenocytes were surface-stained with Mouse CD79b mAb (A25358,2 µg/mL,orange line) or PE Rabbit IgG isotype control (A24172,5 µl/Test,blue line), followed by PE Donkey anti-rabbit Antibody staining. Non-fluorescently stained cells were used as blank control (red line).
Flow cytometry: 1X10 6 C57BL/6 mouse Splenocytes were surface-stained with PE Rabbit IgG isotype control (A24172,5 µl/Test,left) or Mouse CD79b mAb (A25358,2 µg/mL,right).
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