PerCP/Cyanine5.5 anti-mouse CD66a CEACAM1a Antibody anti-CD66a - MAb-CC1,BioLegend,134511

Mab-CC1 clone recognizes the MHV binding domain of CD66a2. Pretreatment of murine fibroblasts with Mab-CC1 prevented binding of MHV-A59 and protected cells from infection with MHV-A592. SJL/J mice are resistant to MHV as they express an alternative allele, clone Mab-CC1 does not react against SJL/J cells2.

Host

Mouse

Reactivity

Mouse

Application

FC - Quality tested

Platform ID

BAB062548107

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Product Specifications
Scientific Background

Specifications

NamePerCP/Cyanine5.5 anti-mouse CD66a CEACAM1a Antibody anti-CD66a - MAb-CC1
Cat. No.134511
HostMouse
RRIDAB_2632798 (BioLegend Cat. No. 134511)AB_2632799 (BioLegend Cat. No. 134512)
IsotypeMouse IgG1, κ
ReactivityMouse
ApplicationFC - Quality tested
ClonalityMonoclonal
Clone NumberMAb-CC1
Concentration0.2 mg/ml
TargetCD66a
ImmunogenSJL/J mice immunized with deoxycholate extracted proteins from BALB/c intestinal brush border membranes.
PurityThe antibody was purified by affinity chromatography and conjugated with PerCP/Cyanine5.5 under optimal conditions.
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and BSA (origin USA)
StorageThe antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light.Do not freeze.
Regulatory StatusResearch Use Only

Scientific Background

CD66a, known as CEACAM1a, carcinoembryonic antigen-related cell adhesion molecule 1a, is a glycoprotein of the immunoglobulin superfamily and the carcinoembryonic antigen family. Isoforms expressing either two or four alternatively spliced Ig-like domains in mice have been found in a number of epithelial, endothelial, or hematopoietic tissues. CEACAM1a functions as an intercellular adhesion molecule, an angiogenic factor, and a tumor cell growth inhibitor. It also serves as a signal regulatory protein influencing B cell receptor complex-mediated activation. The mouse and human CEACAM1a proteins are targets of viral or bacterial pathogens, respectively. It was reported that targeted disruption of the CEACAM1a gene resulting in a partial ablation of the protein in mice led to reduced susceptibility to virus infection. The antibody recognizes the N-terminal domain of murine CEACAM1a, it does not recognize murine CEACAM1b, an allele in SJL mice.

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