![ICC/IF analysis of mouse microglia cells using GTX53229 TREM-2b antibody [5J46]. ICC/IF analysis of mouse microglia cells using GTX53229 TREM-2b antibody [5J46].](https://www.genetex.com/upload/website/prouct_img/normal/GTX53229/GTX53229_20191119_ICCIF_2_w_23060900_367.webp)
ICC/IF analysis of mouse microglia cells using GTX53229 TREM-2b antibody [5J46].
TREM-2b antibody [5J46]
GTX53229
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
ReactivityMouse
TargetTrem2
Overview
- SupplierGeneTex
- Product NameTREM-2b antibody [5J46] - KO/KD Validated
- Delivery Days Customer9
- Application Supplier NoteWB: 1:500 - 1:1000. ICC/IF: 1:50 - 1:100. IHC: 1:50 - 1:100. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone ID5J46
- ConjugateUnconjugated
- Gene ID83433
- Target nameTrem2
- Target descriptiontriggering receptor expressed on myeloid cells 2
- Target synonymsTrem; TREM-2; Trem2a; Trem2b; Trem2c; triggering receptor expressed on monocytes 2; triggering receptor expressed on myeloid cells 2; triggering receptor expressed on myeloid cells 2a; triggering receptor expressed on myeloid cells 2b; triggering receptor expressed on myeloid cells 2c
- HostRat
- IsotypeIgG2
- Protein IDQ99NH8
- Protein NameTriggering receptor expressed on myeloid cells 2
- Scientific DescriptionThe protein encoded by this gene is part of the immunoglobulin and lectin-like superfamily and functions as part of the innate immune system. This gene forms part of a cluster of genes on mouse chromosome 17 thought to be involved in innate immunity. This protein associates with the adaptor protein Dap-12 and recruits several factors, such as kinases and phospholipase C-gamma, to form a receptor signaling complex that activates myeloid cells, including dendritic cells and microglia. In humans homozygous loss-of-function mutations in this gene cause Nasu-Hakola disease and mutations in this gene may be risk factors to the development of Alzheimers disease. In mouse mutations of this gene serve as a pathophysiological model for polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (Nasu-Hakola disease) and for inflammatory bowel disease. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jan 2013]
- ReactivityMouse
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203