CD369 Primary Antibody

Item Information
Catalog # Size/Concentration Price
31709 100ug $341.00
Specification
AliasesCLEC7A; BGR; CANDF4; SCARE2; DECTIN1; CLECSF12
Clone#4G2H2
Entrez GeneID64581
FormulationPurified antibody in PBS with 0.05% sodium azide
HostMouse
IsotypeIgG1
ImmunogenMouse IgG2b
MW98.6kDa
Application
ELISA1/10000
IHC_P (Immunohistochemistry) Purified recombinant fragment of human CD315 (AA: extra 46-221) expressed in E. Coli.
FCM (Flow Cytometry)1/200 - 1/400
Sequence
(AA: extra 66-247) expressed in E. Coli.
Catalog
31709
$341.00
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Images

Figure 1: Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)

Cell Culture Products

Figure 2: Western blot analysis using CD369 mAb against human CD369 (AA: extra 66-247) recombinant protein. (Expected MW is 46.5 kDa)

Cell Culture Products

Figure 3: Western blot analysis using CD369 mAb against HEK293 (1) and CD369 (AA: extra 66-247)-hIgGFc transfected HEK293 (2) cell lysate.

Cell Culture Products

Figure 4: Flow cytometric analysis of HL-60 cells using CD369 mouse mAb (green) and negative control (red).

Cell Culture Products
Tissue Array Results
Position Tissues Name Result Localization
Nucleus Cytoplasm Membrane
E9/10 Endometrial Cancer
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Product Overview
Description

This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. The encoded glycoprotein is a small type II membrane receptor with an extracellular C-type lectin-like domain fold and a cytoplasmic domain with an immunoreceptor tyrosine-based activation motif. It functions as a pattern-recognition receptor that recognizes a variety of beta-1,3-linked and beta-1,6-linked glucans from fungi and plants, and in this way plays a role in innate immune response. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region.

References (references)
References (references) 1.Br J Cancer. 2011 Feb 1;104(3):496-504.
2.J Proteomics. 2009 Nov 2;73(1):93-102.

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