Carboxypeptidase A1 (Pancreatic) (CPA1) antibody (APC)

Details for Product No. ABIN1112254
Antigen
  • cpa1
  • cbpa1
  • CPA
  • CPA1
  • 0910001L12Rik
  • Cpa
  • carboxypeptidase A1
  • pancreatic carboxypeptidase A1
  • Carboxypeptidase A1
  • carboxypeptidase A1-like
  • carboxypeptidase a1
  • carboxypeptidase A1, pancreatic
  • CpipJ_CPIJ007169
  • CpipJ_CPIJ010802
  • CpipJ_CPIJ010805
  • MCYG_06789
  • MGYG_03840
  • cpa1
  • cbpa1
  • LOC100224866
  • CPA1
  • Cpa1
Reactivity
Human
109
41
36
19
2
2
1
1
Host
Mouse
82
47
2
Clonality (Clone)
Monoclonal ()
Conjugate
APC
3
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Application
Flow Cytometry (FACS), Immunofluorescence (IF)
102
46
41
29
20
16
15
14
8
5
5
3
3
3
2
2
2
2
1
Options
Clone CA2
Isotype IgG
Characteristics Monoclonal Mouse Anti-Human Carboxypeptidase A APC for identification of Carboxypeptidase A. CA2 is a mouse monoclonal antibody specific for mast cell carboxypeptidase.
Antigen
Alternative Name CPA (CPA1 Antibody Abstract)
Application Notes It is recommended for use in flow cytometry. This reagent is effective for direct immunofluorescence staining of human tissue for flow cytometric analysis using 20 µl/10^6 cells.
Comment

Allophycocyanin (APC), Abs/Em: 651/662 nm.

Sample Collection 1. Pipette 50 µl of sample to be analysed (up to 10^6 cells) into each tube. 2. For each sample, add an appropriate volume of conjugated antibody (20 µl) directed to the cell surface antigen of interest and the appropriate isotype control. Incubate for 15 minutes in the dark at room temperature. (This step is only necessary is you want to perform a direct immunofluorescence staining for a cell surface antigen) 3. Add 100 µL of Intracell Reagent A, (Fixative), to each tube. Mix gently. 4. Incubate for 15 minutes at room temperature. 5. Wash once in 2 ml PBS Working Solution 1X. 6. Centrifuge for 5 minutes at 300 xg, then aspirate supernatant, leaving approximately 50 µl of fluid and vortex to ensure that the cell pellet are in suspension. 7. Add 100 µL of Intracell Reagent B (Permeabilization), to each tube. 8. Add the appropriate volume of CPA APC for the intracellular antigen and the appropriate isotype control. 9. Incubate for 15 minutes in the dark at room temperature. 10. Wash once in 2 ml PBS Working Solution 1X. 11. Centrifuge for 5 minutes at 300 xg, then aspirate supernatant, leaving approximately 50 µl of fluid and vortex to ensure that the cell pellet are in suspension. 12. Resuspend the cell pellet in 0,5 ml of 1% paraformaldehyde solution or an appropriate fluid for flow cytometric use, and store in the dark at 2-8 °C. Fixed cells should be analyzed within 24 hours.
Restrictions For Research Use only
Format Liquid
Buffer The conjugate is provided in liquid form in buffer containing stabilizer solution, PBS 20 mM and 0,09% Sodium azide, pH 7.2.
Preservative Sodium azide
Precaution of Use 1. The device is not intended for clinical use including diagnosis, prognosis, and monitoring of a disease state, and it must not be used in conjunction with patient records or treatment. 2. This product contains Sodium azide (NaN3), a chemical highly toxic in pure form. At product concentrations, though not classified as hazardous, Sodium azide may react with lead and copper plumbing to form highly explosive build-ups of metal azides. Upon disposal, flush with large volumes of water to prevent metal azide build-up in plumbing. 3. As with any product derived from biological sources, proper handling procedures should be used.
Storage 4 °C
Supplier Images
Image no. 1 for anti-Carboxypeptidase A1 (Pancreatic) (CPA1) antibody (APC) (ABIN1112254) anti-Carboxypeptidase A1 (Pancreatic) (CPA1) antibody (APC)
Product cited in: Austin, Trowsdale, Rudd, Bodmer, Feldmann, Lamb: "Functional expression of HLA-DP genes transfected into mouse fibroblasts." in: Nature, Vol. 313, Issue 5997, pp. 61-4, 1985 (PubMed).

Royston, Omary, Trowbridge: "Monoclonal antibodies to a human T-cell antigen and Ia-like antigen in the characterization of lymphoid leukemia." in: Transplantation proceedings, Vol. 13, Issue 1 Pt 2, pp. 761-6, 1981 (PubMed).

Background publications Watson, DeMars, Trowbridge, Bach: "Detection of a novel human class II HLA antigen." in: Nature, Vol. 304, Issue 5924, pp. 358-61, 1983 (PubMed).

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