Clone:
UCHT2
Type of antibody:
Primary antibodies
Isotype:
mouse IgG1κ
Applications:
FC, MICS, IF, IHC, ICC, MC
Alternative names:
Leu-1, T1, Ly-1, Tp67

Extended validation for CD5 Antibody, anti-human

Specificity

Epitope competition
In order to compare the epitope specificity of an antibody, the clone being used is compared with other known clones recognizing the same antigen in a competition assay.
Other clonesOverlap in epitope recognition with UCHT2
REA782++
L17F12-
M28623-
205919 (mIgG2a)++
Cells were incubated with an excess of purified unconjugated CD5 (UCHT2) antibody followed by staining with fluorochrome-conjugated antibodies of other known clones against the same marker. Based on the fluorescence signal obtained, the clones were identified as recognizing completely overlapping (++), partially overlapping (+), or completely different epitopes (-) of the marker.

Sensitivity

Performance comparison
Selected fluorochrome conjugated antibodies from Miltenyi Biotec were compared to commercially available hybridoma clones in flow cytometry analysis.
View details
Flow cytometric comparison of different clones for CD5. Human peripheral blood mononuclear cells (PBMCs) were stained with CD5 antibodies and with a suitable counterstaining. As a control, CD5 antibody staining was omitted and cells were measured in the same channels. Flow cytometry was performed with the MACSQuant® Analyzer. Cell debris, dead cells, and cell doublets were excluded from the analysis based on scatter signals and 4',6-diamidino-2-phenylindole (DAPI) fluorescence. No FcR Blocking Reagent was used. The recommended titers of respective antibodies from different suppliers were used.
View details
Flow cytometric comparison of different clones for CD5. Human peripheral blood mononuclear cells (PBMCs) were stained with CD5 antibodies and with a suitable counterstaining. As a control, CD5 antibody staining was omitted and cells were measured in the same channels. Flow cytometry was performed with the MACSQuant® Analyzer. Cell debris, dead cells, and cell doublets were excluded from the analysis based on scatter signals and 4',6-diamidino-2-phenylindole (DAPI) fluorescence. No FcR Blocking Reagent was used. The recommended titers of respective antibodies from different suppliers were used.
View details
Flow cytometric comparison of different clones for CD5. Human peripheral blood mononuclear cells (PBMCs) were stained with CD5 antibodies and with a suitable counterstaining. As a control, CD5 antibody staining was omitted and cells were measured in the same channels. Flow cytometry was performed with the MACSQuant® Analyzer. Cell debris, dead cells, and cell doublets were excluded from the analysis based on scatter signals and 4',6-diamidino-2-phenylindole (DAPI) fluorescence. No FcR Blocking Reagent was used. The recommended titers of respective antibodies from different suppliers were used.
View details
Flow cytometric comparison of different clones for CD5. Human peripheral blood mononuclear cells (PBMCs) were stained with CD5 antibodies and with a suitable counterstaining. As a control, CD5 antibody staining was omitted and cells were measured in the same channels. Flow cytometry was performed with the MACSQuant® Analyzer. Cell debris, dead cells, and cell doublets were excluded from the analysis based on scatter signals and 4',6-diamidino-2-phenylindole (DAPI) fluorescence. No FcR Blocking Reagent was used. The recommended titers of respective antibodies from different suppliers were used.
View details
Flow cytometric comparison of different clones for CD5. Human peripheral blood mononuclear cells (PBMCs) were stained with CD5 antibodies and with a suitable counterstaining. As a control, CD5 antibody staining was omitted and cells were measured in the same channels. Flow cytometry was performed with the MACSQuant® Analyzer. Cell debris, dead cells, and cell doublets were excluded from the analysis based on scatter signals and 4',6-diamidino-2-phenylindole (DAPI) fluorescence. No FcR Blocking Reagent was used. The recommended titers of respective antibodies from different suppliers were used.
View details
Flow cytometric comparison of different clones for CD5. Human peripheral blood mononuclear cells (PBMCs) were stained with CD5 antibodies and with a suitable counterstaining. As a control, CD5 antibody staining was omitted and cells were measured in the same channels. Flow cytometry was performed with the MACSQuant® Analyzer. Cell debris, dead cells, and cell doublets were excluded from the analysis based on scatter signals and 4',6-diamidino-2-phenylindole (DAPI) fluorescence. No FcR Blocking Reagent was used. The recommended titers of respective antibodies from different suppliers were used.
Flow cytometric comparison of different clones for CD5. Human peripheral blood mononuclear cells (PBMCs) were stained with CD5 antibodies and with a suitable counterstaining. As a control, CD5 antibody staining was omitted and cells were measured in the same channels. Flow cytometry was performed with the MACSQuant® Analyzer. Cell debris, dead cells, and cell doublets were excluded from the analysis based on scatter signals and 4',6-diamidino-2-phenylindole (DAPI) fluorescence. No FcR Blocking Reagent was used. The recommended titers of respective antibodies from different suppliers were used.
Fixation data
To provide an indication on how an antibody performs after fixation of cells, in-house data on staining results before and after fixation with 3.7% formaldehyde using Miltenyi Biotec antibodies are provided. Different experimental settings may lead to different results.
No fixation
Post fixation
View details
Comparison of staining pattern on non-fixed and fixed cells using CD5 (UCHT2). The performance of the antibody after fixation was tested by comparing the staining pattern on fresh (no fixation) versus fixed (post fixation) cells.
View details
Comparison of staining pattern on non-fixed and fixed cells using CD5 (UCHT2). The performance of the antibody after fixation was tested by comparing the staining pattern on fresh (no fixation) versus fixed (post fixation) cells.
Comparison of staining pattern on non-fixed and fixed cells using CD5 (UCHT2). The performance of the antibody after fixation was tested by comparing the staining pattern on fresh (no fixation) versus fixed (post fixation) cells.

Specifications for CD5 Antibody, anti-human

Overview

Clone UCHT2 reacts with human CD5, a 67 kDa single-chain transmembrane glycoprotein. It is expressed on most thymocytes, the majority of peripheral T cells, a subpopulation of B cells, and B cell chronic lymphocytic leukemia (B-CLL) cells.

Alternative names

Leu-1, T1, Ly-1, Tp67

Detailed product information

Technical specifications

CloneUCHT2
Clonalitymonoclonal
Isotypemouse IgG1κ
Isotype controlIsotype Control Antibody, mouse IgG1
Hostmouse
Type of antibodyPrimary antibodies
Specieshuman, non-human primate
Cross-reactivity
cynomolgus monkey (
Macaca fascicularis
)
,
common marmoset (
Callithrix jacchus
)
,
chimpanzee (
Pan troglodytes
)
, capuchin monkey
AntigenCD5
Alternative names of antigenLeu-1, T1, Ly-1, Tp67
Molecular mass of antigen [kDa]52
Distribution of antigenB cells, lymphocytes, T cells, thymocytes, B cells, T cells, lymphocytes, thymocytes
Entrez Gene ID921
RRIDAB_2733387, AB_2751800, AB_2751740, AB_2751937, AB_2751890, AB_2751938, AB_2751891, AB_2751939, AB_2751892, AB_2784249, AB_2784248, AB_2751936, AB_2751889, AB_2660342, AB_2733386

References for CD5 Antibody, anti-human

Publications

  1. Knapp, W. et al. (eds) Leukocyte Typing IV Oxford, Oxford University Press

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