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Anti-Human CD5 FITC/CD10 PE/CD19 PerCP-Cy™5.5

BD Oncomark™ Anti-Human CD5 FITC/CD10 PE/CD19 PerCP-Cy™5.5

製品詳細
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BD Oncomark™
Human
Flow cytometry
体外診断用医薬品
AB_2075591
Phosphate-buffered saline (PBS) containing gelatin and 0.1% sodium azide.


説明

The CD5 antibody, clone L17F12, is derived from hybridization of NS-1/Ag4 mouse myeloma cells with spleen cells from BALB/c mice immunized with human T-ALL cells.

The CD10 antibody, clone HI10a, is derived from the hybridization of P3-63-Ag8.653 mouse myeloma cells with spleen cells of BALB/c mice immunized with blasts from a patient with acute CALLA leukemia.

The CD19 antibody, clone SJ25C1, is derived from hybridization of Sp2/0 mouse cells with spleen cells from BALB/c mice immunized with NALM1 + NALM16 cells.

The CD5 antibody recognizes a human T-lymphocyte antigen, with a molecular weight of 67 kilodaltons (kDa).

The CD10 antibody (Anti-CALLA) recognizes a human common acute lymphoblastic leukemia antigen (CALLA), with a molecular weight of 100 kDa. The CD10 antigen is identical to human membrane-associated neutral endopeptidase (NEP; EC 3.3.24.11), also known as enkephalinase.

The CD19 antibody (SJ25C1) recognizes a 90-kDa antigen that is present on human B lymphocytes.

調製と保管

Store vials at 2°C–8°C. Conjugated forms should not be frozen. Protect from exposure to light. Each reagent is stable until the expiration date shown on the bottle label when stored as directed.

341138 Rev. 1
構成品
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説明 クローン アイソタイプ EntrezGene ID
N/A N/A | IgG2a, κ,IgG1, κ N/A
341138 Rev. 1

Please refer to Support Documents for Quality Certificates

Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described

Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims.  Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not For Use in Diagnostic Procedures.

RUO/GMP—For Research Use Only. Not for use in diagnostic or therapeutic procedures. Although not required, these products are manufactured in accordance with Good Manufacturing Practices.

23-22943-00