HLA Class II DR Mouse Monoclonal Antibody [Clone ID: 423L]
CAT#: AM05204FC-N
HLA Class II DR mouse monoclonal antibody, clone 423L, FITC
Conjugation: Unconjugated Biotin
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CNY 4,910.00
Cited in 1 publication. |
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Specifications
Product Data | |
Clone Name | 423L |
Applications | FC |
Recommend Dilution | Flow Cytometry. Monitoring of B cells in peripheral blood. Analysis of B subsets. Study of B cell activation. Study of B cell neoplasms. |
Reactivity | Human, Monkey |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | Derived from the hybridization of mouse NS-1/1-Ag4 myeloma cells with spleen cells of BALB/c mice immunized with human lymphoblastoid B-cell line RPMI 8866. |
Specificity | This antibody recats with Human B and T subset Lymphocyte. Other species not tested. |
Formulation | PBS containing 0.2% protein carrier and 0.08% Sodium Azide as preservative. Label: FITC State: Liquid purified IgG fraction |
Concentration | lot specific |
Purification | Protein A/G Chromatography |
Conjugation | FITC |
Storage Condition | Store undiluted at 2-8°C. DO NOT FREEZE! |
Background | Identification of human B cell and T cell subsets associated with approximately 10% of peripheral blood lymphocytes 28-34,000 M.W. surface antigen, also low density on monocytes and macrophages. |
Synonyms | HLA-DR, HLA class II histocompatibility antigen DR, MHC class II antigen DR |
Note | Protocol: PBMC: Add 10 ul of MAB/10e6 PBMC in 100 ul PBS. Mix gently and incubate for 15 minutes at 2-8°C. Wash twice with PBS and analyze or fix with 0.5% v/v of paraformaldehyde in PBS and analyze. WHOLE BLOOD: Add 10 ul of MAB/100 ul of whole blood. Mix gently and incubate for 15 minutes at room temperature (20°C). Lyse the whole blood. Wash once with PBS and analyze or fix with 0.5% v/v of paraformaldehyde in PBS and analyze. See instrument manufacturers instructions for Lysed Whole Blood and Immunofluorescence analysis with a flow cytometer or microscope. |
Reference Data |
Citations (1)
The use of this Antibodies has been cited in the following citations: |
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Proteolytic cleavage of the fusion protein but not membrane fusion is required for measles virus-induced immunosuppression in vitro
,Weidmann A, Maisner A, Garten W, Seufert M, ter Meulen V, Schneider-Schaulies S,
J. Virol.
,PubMed ID 10644371
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