Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations
- Immunocytochemistry [2]
- Flow cytometry [1]
- Other assay [2]
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- Product number
- 42-2900 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- Pannexin 2 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µg
- Concentration
- 0.25 mg/mL
- Storage
- -20°C
Submitted references Pannexin1 channels act downstream of P2X 7 receptors in ATP-induced murine T-cell death.
Hyposmotic stress causes ATP release and stimulates Na,K-ATPase activity in porcine lens.
Shoji KF, Sáez PJ, Harcha PA, Aguila HL, Sáez JC
Channels (Austin, Tex.) 2014;8(2):142-56
Channels (Austin, Tex.) 2014;8(2):142-56
Hyposmotic stress causes ATP release and stimulates Na,K-ATPase activity in porcine lens.
Shahidullah M, Mandal A, Beimgraben C, Delamere NA
Journal of cellular physiology 2012 Apr;227(4):1428-37
Journal of cellular physiology 2012 Apr;227(4):1428-37
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Indirect immunofluorescence staining of GFP-pannexin-2-transfected C6 cells using (A) Zymed (R) Rb anti-Pannexin 2 (Mid) (Product # 42-2900). GFP fluorescence is shown in (B), and the images have been merged in (C). Image courtesy of James Nagy, Ph.D., University of Manitoba, Canada.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescence analysis of Pannexin 2 was done on 90% confluent log phase Caco2 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 Pannexin 2 Rabbit Polyclonal Antibody (Product # 42-2900) at 2 µg/mL 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) at 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 Alexa Fluor® 555 Rhodamine Phalloidin (Product # R415, 1:300). Panel d is a merged image showing membranous localization. Panel e is a no primary antibody control. The images were captured at 60X magnification.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Flow cytometry analysis of Pannexin 2 was done on SH-SY5Y cells. Cells were fixed with 70% ethanol for 10 minutes, permeabilized with 0.25% Triton™ X-100 for 20 minutes, and blocked with 5% BSA for 30 minutes at room temperature. Cells were labeled with Pannexin 2 Rabbit Polyclonal Antibody (422900, red histogram) or with rabbit isotype control (yellow histogram) at 3-5 ug/million cells in 2.5% BSA. After incubation at room temperature for 2 hours, the cells were labeled with Alexa Fluor® 488 Goat Anti-Rabbit Secondary Antibody (A11008) at a dilution of 1:400 for 30 minutes at room temperature. The representative 10,000 cells were acquired and analyzed for each sample using an Attune® Acoustic Focusing Cytometer. The purple histogram represents unstained control cells and the green histogram represents no-primary-antibody control..
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- NULL
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- NULL