MABC959
Anti-CD1d Antibody, clone WTH-1
clone WTH-1, from mouse
Synonym(s):
Antigen-presenting glycoprotein CD1d, CD1d
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Recommended Products
biological source
mouse
Quality Level
antibody form
purified antibody
antibody product type
primary antibodies
clone
WTH-1, monoclonal
species reactivity
mouse, rat
technique(s)
activity assay: suitable
flow cytometry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
isotype
IgG2aκ
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Gene Information
mouse ... Cd1D(110290701)
rat ... Cd1D(104874051)
Related Categories
General description
Antigen-presenting glycoprotein CD1d (UniProt Q63493; also known as CD1D antigen, CD1d1 antigen, T-cell surface glycoprotein CD1d) is encoded by the Cd1d (also known as Cd1d1) gene (Gene ID 25109) in rat species. CD1d is a nonpolymorphic MHC class I-like molecule which presents nonpeptide ligands (e.g. glycolipids) to natrual killer T (NKT) cells. NKT cells are known to have multiple effects on innate and adaptive immune responses and on the development of pathological conditions. In additon to hematopoietic cells, CD1d protein is also reported to be detected in non-lymphatic tissues in rat, such as the exocrine pancreas and Paneth cells. CD1d is initially produced with a signal peptide sequence (a.a. 1-17), the removal of which yields the mature CD1d with a large extracellular region (a.a.18-304), a transmembrane domain (a.a. 305-325), and a short cytoplasmic tail (a.a. 326-336).
Application
This Anti-CD1d Antibody, clone WTH-1 is validated for use in Flow Cytometry, Western Blotting, Immunoprecipitation, Immunohistochemistry and Activity Assay for the detection of CD1d.
Western Blotting Analysis: A representative lot detected endogenous CD1d in rat spleen, thymus, and pancreas tissue homogenates, as well as exogenously expressed murine and rat CD1d in lysates of transfected Raji cells (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Flow Cytometry Analysis: A representative lot detected the surface expression of CD1d on isolated thymocytes from rats and mice, as well as on Raji transfectants expressing murine or rat CD1d (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Immunoprecipitation Analysis: A representative lot immunoprecipitated CD1d from isolated mouse and rat thymocytes, as well as exogenously expressed murine and rat CD1d from transfected Raji cells (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Immunohistochemistry Analysis: A representative lot detected CD1d immunoreactivity using frozen tissue sections from rats and mice (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Activity Assay: A representative lot inhibited CD1d antigen presentation cells from activating type I NK cells using total splenocytes from rats and mice. Clone WTH-1 also blocked mCD1d1-transduced LBB cells from activating co-cultured VIII24.1 murine type II NKT cells, while WTH-1 enhanced XV19.2 murine type II NKT cell activation by mCD1d1-transduced Raji cells (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Application Note: Clone WTH-1 (Cat. No. MABC959) and WTH-2 (Cat. No. MABC960) gave inferior IHC staining in mouse than in rat organs, especially in non-lymphatic tissues. In addition, clone WTH-2 produced a much lower signal in mice than mAb WTH-1. To detect low-grade expression, mouse non-lymphatic organs should be stained using a highly sensitive tyramide amplification procedure with inclusion of C57BL/6 CD1d2/2 mouse organs as negative controls (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Flow Cytometry Analysis: A representative lot detected the surface expression of CD1d on isolated thymocytes from rats and mice, as well as on Raji transfectants expressing murine or rat CD1d (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Immunoprecipitation Analysis: A representative lot immunoprecipitated CD1d from isolated mouse and rat thymocytes, as well as exogenously expressed murine and rat CD1d from transfected Raji cells (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Immunohistochemistry Analysis: A representative lot detected CD1d immunoreactivity using frozen tissue sections from rats and mice (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Activity Assay: A representative lot inhibited CD1d antigen presentation cells from activating type I NK cells using total splenocytes from rats and mice. Clone WTH-1 also blocked mCD1d1-transduced LBB cells from activating co-cultured VIII24.1 murine type II NKT cells, while WTH-1 enhanced XV19.2 murine type II NKT cell activation by mCD1d1-transduced Raji cells (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Application Note: Clone WTH-1 (Cat. No. MABC959) and WTH-2 (Cat. No. MABC960) gave inferior IHC staining in mouse than in rat organs, especially in non-lymphatic tissues. In addition, clone WTH-2 produced a much lower signal in mice than mAb WTH-1. To detect low-grade expression, mouse non-lymphatic organs should be stained using a highly sensitive tyramide amplification procedure with inclusion of C57BL/6 CD1d2/2 mouse organs as negative controls (Monzon-Casanova, E., et al. (2010). PLoS One. 5(9): e13089).
Quality
Evaluated by Flow Cytometry in rat thymocytes and splenocytes.
Flow Cytometry Analysis: 1.0 µg of this antibody detected CD1d in rat thymocytes and splenocytes.
Flow Cytometry Analysis: 1.0 µg of this antibody detected CD1d in rat thymocytes and splenocytes.
Target description
~38 kDa calculated
Physical form
Format: Purified
Other Notes
Concentration: Please refer to lot specific datasheet.
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Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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CD1d expression in paneth cells and rat exocrine pancreas revealed by novel monoclonal antibodies which differentially affect NKT cell activation.
Monzon-Casanova, E; Steiniger, B; Schweigle, S; Clemen, H; Zdzieblo, D; Starick et al.
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