PE-Mouse CD1d Tetramer - Negative Control

CAT#: MHC-YF794

This product is a tetramer of CD1d tetramer loaded with no ligand and fluorescent-labeled with PE. It can not bind to mouse NKT cells, as a negative control. Also, this negative control can be used for low frequency positive populations to be accurately quantified.

Gene Expression
Figure 1 IF staining of human cell line HEK 293 Figure 2 IF staining of human cell line HaCaT Figure 3 IF staining of human cell line U-2 OS Figure 4 Cerebral cortex Figure 5 Colon Figure 6 Testis Figure 7 Lymph node Figure 8 Spleen

Specifications

  • Allele
  • CD1d
  • Class
  • Non-classical MHC
  • MHC Species
  • Human
  • Antigen Species
  • Mouse
  • Conjugate
  • PE
  • Application
  • FCM
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Breast cancer biomarkers at key points during disease progression
Essential CD1d Negative Control
This unloaded CD1d tetramer is a crucial negative control for our NKT cell research. Labeled with PE, it allows us to accurately determine background staining and validate the specificity of our ligand-loaded tetramers in mouse samples.
Breast cancer biomarkers at key points during disease progression
Critical For Accurate Gating
We use this negative control reagent in every flow cytometry panel involving CD1d. It ensures that the populations we identify with loaded tetramers are genuine. The product is consistent and behaves exactly as expected for a control reagent.

Q&As

  1. Why is this CD1d tetramer considered a negative control?

    A: This CD1d tetramer is loaded with no ligand (empty). Because it lacks the specific antigen required to engage the NKT cell receptor, it does not bind to mouse NKT cells and serves as a negative control to assess background staining.

  2. What species is this CD1d molecule derived from?

    A: This CD1d molecule is derived from Mouse. It is a non-classical MHC molecule that presents glycolipid antigens, and this specific control product is used in murine NKT cell research.

View the frequently asked questions answered by Creative Biolabs Support.

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