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宿主来源
Rat抗原名称
CD301分子别名
C-type lectin domain family 10 member A; MMGL; Macrophage asialoglycoprotein-binding protein 1 (M-ASGP-BP-1); Macrophage galactose/N-acetylgalactosamine-specific lectin; Mgl; Mgl1; Clec10a细胞定位
MembraneAccession
P49300克隆号
S-R708抗体类型
Rat mAb抗体同种型
IgG2b,k反应种属 ?
Ms阳性样本
BMDC纯化方式
Protein G浓度
2 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS pH7.4
储存条件
12 months from date of receipt / reconstitution, 2 to 8 °C as supplied
应用
FCM
稀释度
应用 稀释度 推荐种属 FCM 1:200 Ms
CD301, also known as CLEC10A (C-type lectin domain family 10 member A) or MGL (Macrophage Galactose-type C-type Lectin), is a 30–40 kDa type II transmembrane glycoprotein belonging to the C-type lectin superfamily that functions as a calcium-dependent pattern recognition receptor and endocytic receptor predominantly expressed on macrophages, immature myeloid dendritic cells, Langerhans cells, and alternatively activated (tolerogenic) macrophages. Structurally, it features a short cytoplasmic tail containing an endocytosis motif (YxxΦ), a single transmembrane domain, and an extracellular carbohydrate recognition domain (CRD) that exhibits unique specificity for terminal nonsialylated N-acetylgalactosamine (GalNAc) and galactose residues, including the tumor-associated Tn antigen and Lewis structures, enabling it to distinguish between healthy and malignant tissues while recognizing pathogenic glycans from bacteria, parasites, and viruses such as Ebola and Marburg. Through binding these carbohydrate ligands, CD301 orchestrates diverse immunological functions: it mediates antigen internalization and presentation via MHC molecules to bridge innate and adaptive immunity, modulates immune responses by inducing interleukin-10 production and regulating T cell activation or apoptosis, and plays dual roles in promoting either immune tolerance or anti-tumor immunity depending on context. Additionally, CD301 is implicated in metabolic regulation through its expression on adipose tissue macrophages where it influences monocyte trafficking and phenotypic switching in obesity, and genetic variants have been associated with type 2 diabetes susceptibility, highlighting its significance as a potential therapeutic target for cancer immunotherapy, infectious disease control, and metabolic disorders.
流式分析
Flow cytometric analysis of BMDC (Bone Marrow-Derived Dendritic Cells) labelling Mouse CD301 antibody at 1/200 dilution (1 μg) / (right panel) compared with a Rat IgG2b, κ Isotype Control / (left panel). Goat Anti-Rat IgG Alexa Fluor® 647 was used as the secondary antibody. Then cells were stained with CD11c - PE antibody separately. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.







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