TREM2 Protein (AA 19-174) (Fc Tag)
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- Target See all TREM2 Proteins
- TREM2 (Triggering Receptor Expressed On Myeloid Cells 2 (TREM2))
- Protein Type
- Recombinant
- Protein Characteristics
- AA 19-174
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Origin
- Cynomolgus
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Source
- Mammalian Cells
- Purification tag / Conjugate
- This TREM2 protein is labelled with Fc Tag.
- Purpose
- Recombinant Cynomolgus TREM2 protein with C-terminal human Fc tag
- Specificity
- TREM2 (His19-Ser174) hFc (Glu99-Ala330)
- Characteristics
- Extracellular Domain Protein
- Purification
- Purified from cell culture supernatant by affinity chromatography
- Purity
- The purity of the protein is greater than 90 % as determined by SDS-PAGE and Coomassie blue staining.
- Top Product
- Discover our top product TREM2 Protein
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- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Buffer
- Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.
- Storage
- -20 °C,-80 °C
- Storage Comment
- Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.
- Expiry Date
- 12 months
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- Target
- TREM2 (Triggering Receptor Expressed On Myeloid Cells 2 (TREM2))
- Alternative Name
- TREM2 (TREM2 Products)
- Synonyms
- TREM-A1 Protein, TREM-B1 Protein, TREM2 Protein, trem-2 Protein, trem2a Protein, trem2b Protein, trem2c Protein, TREM-2 Protein, Trem2a Protein, Trem2b Protein, Trem2c Protein, triggering receptor expressed on myeloid cells 2 Protein, trem-like transcript 2 protein Protein, TREM2 Protein, trem2 Protein, LOC100228399 Protein, Trem2 Protein
- Background
- This gene encodes a membrane protein that forms a receptor signaling complex with the TYRO protein tyrosine kinase binding protein. The encoded protein functions in immune response and may be involved in chronic inflammation by triggering the production of constitutive inflammatory cytokines. Defects in this gene are a cause of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2012]
- Molecular Weight
- predicted molecular mass of 43.6 kDa after removal of the signal peptide.
- NCBI Accession
- XP_015304909
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