PE-labled CD43 Mouse Monoclonal Antibody(ARA652)

Key features and details

  • Reactivity: Human
  • Label: PE
  • Application: IF, FC
  • Host: Mouse
  • Clonality: Monoclonal
  • Target: CD43
  • Brand:
CAT.NO. : ARA6362
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Product Details
Background
Cluster of Differentiation 43 (CD43), also known as Sialophorin, is a transmembrane protein that plays a role in T-cell activation. CD43 is normally expressed abundantly on the surface of differentiated hematopoietic stem cells, including monocytes, granulocytes, T-lymphocytes, and some B-lymphocytes. Due to the efficacy of CD43 immunohistochemical staining in granulocytes, it is an effective marker for myeloid tumours, while other antibodies demonstrate weak staining under these conditions. Given the low reactivity of Anti-CD43 with B-cells, positive staining of CD43 is implicated in a number of lymphoid and myeloid tumours, with over 90% positive staining in T-cell lymphomas. When CD43 is used in combination with CD45 and L26, immunotyping of various lymphomas can be obtained; this is particularly true when co staining a lymphoid infiltrate with CD20 and CD3.
Overview

Product Description

Mouse monoclonal antibody PE labled to CD43

Immunogen

MV4-11 cell line

Purification Method

The antibody was purified by affinity chromatography.

Clonality

Monoclonal

Conjugate

PE

Form

Mouse IgG1 kappa. Liquid in PBS, pH 7.3, 0.2% BSA, and 0.02% sodium azide.

Dilution Ratio

10 μl / assay

Gene Symbol

SPN

Alternative Names

CD43; Leukosialin; Galactoglycoprotein; GALGP; Leukocyte sialoglycoprotein; Sialophorin; CD43

Gene ID (Human)

6693

Protein ID (Human)

P16150

Application Protocol

1. Take 100 μl peripheral blood anticoagulated by EDTA and add to the bottom of 5 ml tube. 2. Add 10 μl labeled antibody to the bottom of flow tube mixing with the whole blood, incubate for 20 minutes at room temperature away from light. 3. Add 2 ml RBC lysis buffer, incubate for 10 minutes away from light after mixing, dissolve red blood cells. 4. Sample tube is set to 1000 rpm centrifugation for 5 minutes, discard the supernatant. 5. Add 2 ml PBS wash buffer to resuspend the cells, then 1000 rpm centrifugation for 5 minutes, discard the supernatant. 6. Add 0.5 ml PBS wash buffer to resuspend the cells and detect by flow cytometry (sample should be determined on the day on the machine and can also be added fixation overnight at 4 °C then measured).

Storage
Store at 4°C , avoiding freeze/thaw cycles.
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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