BD OptiBuild™ BUV661 Mouse Anti-Armenian and Syrian Hamster IgG

IgG

Mouse BALB/c IgG1, κ

Pooled Armenian and Syrian hamster IgG mAb

Based on ELISA analysis, the G192-1 monoclonal antibody reacts specifically with Armenian hamster IgG2, IgG3, and IgG4, and Syrian hamster IgG2 monoclonal antibodies. The G192-1 mAb does not react with other hamster IgG groups or hamster IgM. The antibody was conjugated to BD Horizon™ BUV661 which is part of the BD Horizon Brilliant™ Ultraviolet family of dyes. This dye is a tandem fluorochrome of BD Horizon BUV395 with an Ex Max of 348-nm and an acceptor dye with an Em Max at 661-nm. BD Horizon Brilliant BUV661 can be excited by the ultraviolet laser (355 nm) and detected with a 670/25 filter and a 630 nm LP.  Due to cross laser excitation of this dye, there may be significant spillover into channels detecting APC-like emissions (eg, 670/25-nm filter).      Due to spectral differences between labeled cells and beads, using BD™ CompBeads can result in incorrect spillover values when used with BD Horizon BUV661 reagents. Therefore, the use of BD CompBeads or BD CompBeads Plus to determine spillover values for these reagents is not recommended. Different BUV661 reagents (eg, CD4 vs. CD45) can have slightly different fluorescence spillover therefore, it may also be necessary to use clone-specific compensation controls when using these reagents.

G192-1 Based on ELISA analysis, the G192-1 monoclonal antibody reacts specifically with Armenian hamster IgG2, IgG3, and IgG4, and Syrian hamster IgG2 monoclonal antibodies. The G192-1 mAb does not react with other hamster IgG groups or hamster IgM. The antibody was conjugated to BD Horizon™ BUV661 which is part of the BD Horizon Brilliant™ Ultraviolet family of dyes. This dye is a tandem fluorochrome of BD Horizon BUV395 with an Ex Max of 348-nm and an acceptor dye with an Em Max at 661-nm. BD Horizon Brilliant BUV661 can be excited by the ultraviolet laser (355 nm) and detected with a 670/25 filter and a 630 nm LP.  Due to cross laser excitation of this dye, there may be significant spillover into channels detecting APC-like emissions (eg, 670/25-nm filter). Due to spectral differences between labeled cells and beads, using BD™ CompBeads can result in incorrect spillover values when used with BD Horizon BUV661 reagents. Therefore, the use of BD CompBeads or BD CompBeads Plus to determine spillover values for these reagents is not recommended. Different BUV661 reagents (eg, CD4 vs. CD45) can have slightly different fluorescence spillover therefore, it may also be necessary to use clone-specific compensation controls when using these reagents.

Mouse BALB/c IgG1, κ

克隆 G192-1 (RUO)

0.2 mg/ml

Flow cytometry (Qualified)

Hamster (Tested in Development)

IgG

Aqueous buffered solution containing ≤0.09% sodium azide.

研发参考(2) 1. Heinzel FP, Rerko RM, Hujer AM. Underproduction of interleukin-12 in susceptible mice during progressive leishmaniasis is due to decreased CD40 activity.. Cell Immunol. 1998; 184(2):129-42. (Clone-specific: Flow cytometry). 2. Wang W, Fang K, Li MC, et al. A biodegradable killer microparticle to selectively deplete antigen-specific T cells in vitro and in vivo. Oncotarget. 2016; 7(11):12176-90. (Clone-specific: Flow cytometry).