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- Antibody Data
- Antigen structure
- References [1]
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- Validations
- Immunocytochemistry [2]
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- Product number
- PA3-201 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- CCKBR Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- PA3-201 detects CCK2 in human samples. PA3-201 has successfully been used in Western blot and immunocytochemical procedures. The PA3-201 immunogen is a synthetic peptide corresponding to the C-terminal amino acids R(428)ALPDEDPPTPSIASLSRLSYTTISTLGPG(447) of human CCK2.
- Reactivity
- Human
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 μL
- Concentration
- Conc. Not Determined
- Storage
- -20°C, Avoid Freeze/Thaw Cycles
Submitted references Immunohistochemical localization of CCK1 cholecystokinin receptors in normal and neoplastic human tissues.
Schulz S, Röcken C, Mawrin C, Schulz S
The Journal of clinical endocrinology and metabolism 2005 Nov;90(11):6149-55
The Journal of clinical endocrinology and metabolism 2005 Nov;90(11):6149-55
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescence analysis of CCK2 cholecystokinin receptor 2 was performed using 70% confluent log phase Panc- 1 cells. The cells were fixed with 4% paraformaldehyde for 10 minutes, permeabilized with 0.1% Triton™ X-100 for 10 minutes, and blocked with 1% BSA for 1 hour at room temperature. The cells were labeled with CCK2 cholecystokinin receptor 2 Rabbit Polyclonal Antibody (Product # PA3-201) at 1:250 dilution in 0.1% BSA and incubated for 3 hours at room temperature and then labeled with Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, Alexa Fluor® 488 conjugate (Product # A27034) a dilution of 1:2000 for 45 minutes at room temperature (Panel a: green). Nuclei (Panel b: blue) were stained with SlowFade® Gold Antifade Mountant with DAPI (Product # S36938). F-actin (Panel c: red) was stained with Rhodamine Phalloidin (Product # R415, 1:300). Panel d represents the merged image showing cytoplasmic localization. Panel e shows the no primary antibody control. The images were captured at 60X magnification.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescence analysis of CCK2 cholecystokinin receptor 2 was performed using 70% confluent log phase Panc- 1 cells. The cells were fixed with 4% paraformaldehyde for 10 minutes, permeabilized with 0.1% Triton™ X-100 for 10 minutes, and blocked with 1% BSA for 1 hour at room temperature. The cells were labeled with CCK2 cholecystokinin receptor 2 Rabbit Polyclonal Antibody (Product # PA3-201) at 1:250 dilution in 0.1% BSA and incubated for 3 hours at room temperature and then labeled with Goat anti-Rabbit IgG (Heavy Chain) Superclonal™ Secondary Antibody, Alexa Fluor® 488 conjugate (Product # A27034) a dilution of 1:2000 for 45 minutes at room temperature (Panel a: green). Nuclei (Panel b: blue) were stained with SlowFade® Gold Antifade Mountant with DAPI (Product # S36938). F-actin (Panel c: red) was stained with Rhodamine Phalloidin (Product # R415, 1:300). Panel d represents the merged image showing cytoplasmic localization. Panel e shows the no primary antibody control. The images were captured at 60X magnification.
