product summary
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company name :
MyBioSource
product type :
antibody
product name :
Goat Polyclonal to Human TREM2 / TREM-2
catalog :
MBS242024
quantity :
0.05 mg
price :
495 USD
clonality :
polyclonal
host :
goat
conjugate :
nonconjugated
reactivity :
human
application :
ELISA, immunohistochemistry, enzyme immunoassay
more info or order :
product information
catalog number :
MBS242024
products type :
Antibody
products full name :
Goat Polyclonal to Human TREM2 / TREM-2
products short name :
TREM2 / TREM-2
products name syn :
Anti-TREM2 / TREM-2 Antibody (C-Terminus) IHC-plus; TREM2; Trem2b; TREM-2; Trem2a; Trem2c; Human TREM2; TREM-2
other names :
triggering receptor expressed on myeloid cells 2 isoform 1; Triggering receptor expressed on myeloid cells 2; triggering receptor expressed on myeloid cells 2; triggering receptor expressed on monocytes 2; triggering receptor expressed on myeloid cells 2a; triggering receptor expressed on myeloid cells 2; Triggering receptor expressed on monocytes 2
products gene name :
TREM2
products gene name syn :
TREM-2
other gene names :
TREM2; TREM2; TREM-2; Trem2a; Trem2b; Trem2c; TREM-2
uniprot entry name :
TREM2_HUMAN
clonality :
Polyclonal
host :
Goat
reactivity :
Human. Predicted Reactivity: Gorilla, Gibbon, Monkey (at least 90% immunogen sequence identity)
sequence length :
230
specificity :
Human TREM2.
purity :
Immunoaffinity Purified
form :
Tris-buffered saline, pH 7.3, 0.5% BSA, 0.02% sodium azide
concentration :
0.5 mg/ml
storage stability :
Store at -20 degree C. Minimize freezing and thawing.
tested application :
Immunohistochemistry (IHC - Paraffin), ELISA (EIA)
app notes :
ELISA (1:32000), IHC-P (2.5 ug/ml). Usage: Immunohistochemistry: was validated for use in immunohistochemistry on a panel of 21 formalin-fixed, paraffin-embedded (FFPE) human tissues after heat induced antigen retrieval in pH 6.0 citrate buffer. After incubation with the primary anti.
other info1 :
Target Species: Human. Immunogen Description: Synthetic peptide C-HGQKPGTHPPSELD from the C-terminus of human TREM2 (NP_061838.1). Percent identity with other species by BLAST analysis: Human (100%), Gorilla (93%), Gibbon (93%), Monkey (93%).
other info2 :
Immunogen Type: Synthetic peptide. Immunogen: TREM2 / TREM-2 antibody was raised against synthetic peptide C-HGQKPGTHPPSELD from the C-terminus of human TREM2 (NP_061838.1). Percent identity with other species by BLAST analysis: Human (100%), Gorilla (93%), Gibbon (93%), Monkey (93%). Antigen Modification: C-Terminus
ncbi gi num :
9507203
ncbi acc num :
NP_061838.1
ncbi gb acc num :
NM_018965.3
uniprot acc num :
Q9NZC2
ncbi mol weight :
24,669 Da
ncbi pathways :
Axon Guidance Pathway (105688); DAP12 Interactions Pathway (685549); DAP12 Signaling Pathway (685550); Developmental Biology Pathway (477129); Immune System Pathway (106386); Innate Immune System Pathway (106387); Osteoclast Differentiation Pathway (193147); Osteoclast Differentiation Pathway (193096); Other Semaphorin Interactions Pathway (119526); Semaphorin Interactions Pathway (119519)
ncbi summary :
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]
uniprot summary :
TREM2: May have a role in chronic inflammations and may stimulate production of constitutive rather than inflammatory chemokines and cytokines. Forms a receptor signaling complex with TYROBP and triggers activation of the immune responses in macrophages and dendritic cells. Defects in TREM2 are a cause of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL); also known as presenile dementia with bone cysts or Nasu-Hakola disease (NHD). PLOSL is a recessively inherited disease characterized by a combination of psychotic symptoms rapidly progressing to presenile dementia and bone cysts restricted to wrists and ankles. PLOSL has a global distribution, although most of the patients have been diagnosed in Finland and Japan, with an estimated population prevalence of 2x10(-6) in the Finns. 3 isoforms of the human protein are produced by alternative splicing. Protein type: Membrane protein, integral. Chromosomal Location of Human Ortholog: 6p21.1. Cellular Component: intracellular membrane-bound organelle; extracellular region; plasma membrane; integral to membrane. Molecular Function: peptidoglycan binding; lipopolysaccharide binding; receptor activity. Biological Process: axon guidance; positive regulation of peptidyl-tyrosine phosphorylation; detection of lipopolysaccharide; detection of peptidoglycan; innate immune response; positive regulation of calcium-mediated signaling; humoral immune response; positive regulation of antigen processing and presentation of peptide antigen via MHC class II. Disease: Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy
size1 :
0.05 mg
price1 :
495 USD
more info or order :
company information
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-888-627-0165
headquarters: USA
MyBioSource, LLC was orginally founded in Vancouver by three enthusiastic scientists who are passionate about providing the world with the best reagents available. Together, they form a company with a big vision known as MyBioSource. MyBioSource is now located in San Diego, California, USA.

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