Weight | 1 lbs |
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Dimensions | 9 × 5 × 2 in |
host | mouse |
isotype | IgG |
clonality | monoclonal |
concentration | concentrate, predilute |
applications | IHC |
reactivity | human |
available size | 0.1 mL, 0.5 mL, 1 mL concentrated, 7 mL prediluted |
rabbit anti-Langerin monoclonal antibody (ZR170) 6240
$160.00 – $528.00
Antibody summary
- Rabbit monoclonal to Langerin
- Suitable for: Immunohistochemistry (formalin-fixed, paraffin-embedded tissues)
- Reacts with: Human
- Isotype:IgG
- Control: skin/Langerhans cell histiocytosis
- Visualization: cell surface/cytoplasm.
- 0.1, 0.5, 1.0 mL concentrated, 7 mL prediluted
rabbit anti-Langerin monoclonal antibody ZR170 6240
target relevance |
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Protein names C-type lectin domain family 4 member K (Langerin) (CD antigen CD207) |
Mass 36725Da |
Function Calcium-dependent lectin displaying mannose-binding specificity. Induces the formation of Birbeck granules (BGs); is a potent regulator of membrane superimposition and zippering. Binds to sulfated as well as mannosylated glycans, keratan sulfate (KS) and beta-glucans. Facilitates uptake of antigens and is involved in the routing and/or processing of antigen for presentation to T cells. Major receptor on primary Langerhans cells for Candida species, Saccharomyces species, and Malassezia furfur. Protects against human immunodeficiency virus-1 (HIV-1) infection. Binds to high-mannose structures present on the envelope glycoprotein which is followed by subsequent targeting of the virus to the Birbeck granules leading to its rapid degradation. |
Subellular location Membrane ; Single-pass type II membrane protein . Note=Found in Birbeck granules (BGs), which are organelles consisting of superimposed and zippered membranes. |
Tissues Exclusively expressed by Langerhans cells. Expressed in astrocytoma and malignant ependymoma, but not in normal brain tissues. |
Structure Homotrimer. |
Domain DOMAIN 202..320; /note="C-type lectin"; /evidence="ECO:0000255|PROSITE-ProRule:PRU00040" |
Involvement in disease Birbeck granule deficiency (BIRGD) [MIM:613393]: A condition characterized by the absence of Birbeck granules in epidermal Langerhans cells. Despite the lack of Birbeck granules, Langerhans cells are present in normal numbers and have normal morphologic characteristics and antigen-presenting capacity. Note=The disease is caused by variants affecting the gene represented in this entry. |
Target Relevance information above includes information from UniProt accession: Q9UJ71 |
The UniProt Consortium |
Data
Formalin-fixed, paraffin-embedded human Langerhans cell histiocytosis stained with anti-langerin antibody using peroxidase-conjugate and DAB chromogen. Note cytoplasmic staining of tumor cells |
Publications
Published literature highly relevant to the biological target of this product and referencing this antibody or clone are retrieved from PubMed database provided by The United States National Library of Medicine at the National Institutes of Health.pmid | title | authors | citation |
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Protocols
relevant to this product |
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IHC |
Documents
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