CLEC4E Mouse Monoclonal Antibody [Clone ID: AT16E3]
CAT#: AM09361PU-S
CLEC4E mouse monoclonal antibody, clone AT16E3, Purified
Size: 100 ul
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CNY 5,630.00
货期*
5周
规格
Cited in 1 publication. |
Specifications
Product Data | |
Clone Name | AT16E3 |
Applications | ELISA, IF, IHC, WB |
Recommend Dilution | ELISA. Western blot: 1/250-1/1000. Immunofluorescence: 1/250-1/500. Immunohistochemistry on Paraffin Embedded tissues: 1/50. |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | Recombinant Human MINCLE (41-219aa) purified from E. coli |
Specificity | The antibody recognizes Human CLEC4E (MINCLE). Other species not tested. |
Formulation | PBS, pH 7.4 containing 0.02% Sodium Azide and 10% Glycerol State: Purified State: Liquid purified Ig fraction |
Concentration | lot specific |
Purification | Protein-G Affinity Chromatography |
Conjugation | Unconjugated |
Storage Condition | Store undiluted at 2-8°C for up to two weeks or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Gene Name | C-type lectin domain family 4 member E |
Database Link | |
Background | MINCLE (macrophage inducible C-type lectin, also called CLEC4E or CLECSF9), which is a diverse family of protein which was originally defined by their ability to recognize a wide range of ligand of carbohydrate structure. MINCLE expressed in macrophages subjected to several types of stress. It plays an essential role in response to trehalose-6,6'-dimycolate (TDM) and activated by a synthetic analogue, trehalose dibehenate (TDB). Recently it was reported that MINCLE is associated with an immunoreceptor tyrosine-based activation motif–containing Fc receptor γ chain (FcRγ) and functions as an activating receptor for damaged self- and non–self-pathogenic fungi. |
Synonyms | CLECSF9, MINCLE |
Reference Data | |
Protein Families | Druggable Genome, Transmembrane |
Citations (1)
The use of this Antibodies has been cited in the following citations: |
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The necrosome promotes pancreatic oncogenesis via CXCL1 and Mincle-induced immune suppression
,Seifert L, Werba G, Tiwari S, Giao Ly NN, Alothman S, Alqunaibit D, Avanzi A, Barilla R, Daley D, Greco SH, Torres-Hernandez A, Pergamo M, Ochi A, Zambirinis CP, Pansari M, Rendon M, Tippens D, Hundeyin M, Mani VR, Hajdu C, Engle D, Miller G,
Nature
,PubMed ID 27049944
[CLEC4E]
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