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[My Biosource 공식 대리점]-anti-CD207 antibody :: Mouse anti-Human Langerin Monoclonal Antibody,anti-CD207 항체 :: 마우스 항-인간 랑게린 단일클론 항체(MBS370265)
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anti-CD207 antibody :: Mouse anti-Human Langerin Monoclonal Antibody
CATALOG # : MBS370265
Product Name:Langerin (CD207), Monoclonal Antibody
Full Product Name:Langerin
Product Gene Name:anti-CD207 antibody[Similar Products]
Research Use Only:For Research Use Only. Not for use in diagnostic procedures.
Molecular Weight:36,725 Da
Chromosome Location:Chromosome: 2; NC_000002.11 (71057343..71062953, complement). Location: 2p13
OMIM:604862
3D Structure:ModBase 3D Structure for Q9UJ71
Clonality:Monoclonal
Isotype:IgG2b
Clone Number:12D6
Host:Mouse
Species Reactivity:Human
Preparation and Storage:Store at 2 to 8 degree C in the dark.
ISO Certification:Manufactured in an ISO 13485:2016 Certified Laboratory.
Other Notes: Small volumes of anti-CD207 antibody vial(s) may occasionally become entrapped
in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the
vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may
require to ship with dry ice and additional dry ice fee may apply.
NCBI/Uniprot data below describe general gene information for CD207. It may not necessarily
be applicable to this product.
NCBI GI #:6523279
NCBI GeneID:50489
NCBI Accession #:CAB62403.1
UniProt Primary Accession #:Q9UJ71
UniProt Related Accession #:Q9UJ71
NCBI Official Full Name:langerin
NCBI Official Synonym Full Names:CD207 molecule, langerin
NCBI Official Symbol:CD207
NCBI Official Synonym Symbols:CLEC4K
NCBI Protein Information
C-type lectin domain family 4 member K; CD207 antigen, langerin; Langerhans cell specific
c-type lectin; C-type lectin domain family 4, member K
UniProt Protein Name:C-type lectin domain family 4 member K
UniProt Synonym Protein Names:Langerin
Protein Family:C-type lectin domain family
UniProt Gene Name:CD207
UniProt Synonym Gene Names:CLEC4K
UniProt Entry Name:CLC4K_HUMAN
NCBI Summary for CD207
The protein encoded by this gene is expressed only in Langerhans cells which are immature dendritic
cells of the epidermis and mucosa. It is localized in the Birbeck granules, organelles present in the
cytoplasm of Langerhans cells and consisting of superimposed and zippered membranes. It is a C-type
lectin with mannose binding specificity, and it has been proposed that mannose binding by this protein
leads to internalization of antigen into Birbeck granules and providing access to a nonclassical antigen-
processing pathway. Mutations in this gene result in Birbeck granules deficiency or loss of sugar binding
activity. [provided by RefSeq, Aug 2010]
UniProt Comments for CD207
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. Ref.1 Ref.6 Ref.8 Ref.9
Subunit structure: Homotrimer. Ref.4
Subcellular location: Membrane; Single-pass type II membrane protein. Note:
Found in Birbeck granules (BGs), which are organelles consisting of superimposed and zippered membranes. Ref.1
Tissue specificity: Exclusively expressed by Langerhans cells. Expressed in astrocytoma and malignant
ependymoma, but not in normal brain tissues. Ref.1 Ref.8
Domain: The C-type lectin domain mediates dual recognition of both sulfated and mannosylated glycans. Ref.8
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 mutations affecting the gene represented in this entry. Ref.11 Ref.12
Sequence similarities: Contains 1 C-type lectin domain.
Research Articles on CD207
1. binding properties of langerin
Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic,
therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to
MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance
with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process
any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet,
MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the
right to make changes to this datasheet at any time without prior notice.
It is the responsibility of the customer to report product performance issues to MyBioSource within
30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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