Antibody data
- Antibody Data
- Antigen structure
- References [1]
- Comments [0]
- Validations
- Western blot [2]
- Immunohistochemistry [1]
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Validation data
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- Product number
- MA3-003 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- BAP31 Monoclonal Antibody (CC-4)
- Antibody type
- Monoclonal
- Antigen
- Other
- Description
- MA3-003 detects BAP31 from human, non-human primate, bovine and hamster samples. MA3-003 has been successfully used in Western blot, immunofluorescent, and immunohistochemical procedures. By Western blot, this antibody detects a 28-kDa protein corresponding to human BAP31. The MA3-003 antigen is solubilized protein from human neuroendocrine cell line IMR-32, followed by an extract of the small lung human carcinoma cell line SCC-9. MA3-003 binds to a more proximal region of BAP31 (amino acids 123-229). This sequence is conserved in non-human primate, bovine and hamster species.
- Reactivity
- Human, Bovine, Hamster
- Host
- Rat
- Isotype
- IgG
- Antibody clone number
- CC-4
- Vial size
- 100 µL
- Concentration
- Conc. Not Determined
- Storage
- -20° C, Avoid Freeze/Thaw Cycles
Submitted references Association of BAP31 with CD11b/CD18. Potential role in intracellular trafficking of CD11b/CD18 in neutrophils.
Zen K, Utech M, Liu Y, Soto I, Nusrat A, Parkos CA
The Journal of biological chemistry 2004 Oct 22;279(43):44924-30
The Journal of biological chemistry 2004 Oct 22;279(43):44924-30
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis was performed on membrane enriched extracts (30µg lysate) of COS-7 (Lane 1), Raji (Lane 2), Molt-4 (Lane 3), HeLa (Lane 4), MCF7 (Lane 5), K-562 (Lane6), Hep G2 (Lane 7), Jurkat (Lane 8), HT-1080 (Lane 9) and HEK-293 (Lane 10). The blots were probed with anti-BAP31 Rat Monoclonal Antibody (Product # MA3-003, 1:1500 dilution) and detected by chemiluminescence using Goat anti-Rat IgG2a Secondary Antibody, HRP conjugate (Product # PA1-84709, 0.4µg/mL, 1:2500 dilution). A 28 kDa band corresponding to BAP31 was observed across tissues tested. Known quantity of protein samples were electrophoresed using Novex® NuPAGE® 4-12 % Bis-Tris gel (Product # NP0322BOX), XCell SureLock™ Electrophoresis System (Product # EI0002) and Novex® Sharp Pre-Stained Protein Standard (Product # LC5800). Resolved proteins were then transferred onto a nitrocellulose membrane with iBlot® 2 Dry Blotting System (Product # IB21001). The membrane was probed with the relevant primary and secondary Antibody following blocking with 5% skimmed milk. Chemiluminescent detection was performed using Pierce™ ECL Western Blotting Substrate (Product # 32106).
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Knockdown of BAP31 was achieved by transfecting HeLa cells with BAP31 specific siRNAs (Silencer® select Product # s19722, s19721). Western blot analysis (Fig a) was performed using membrane enriched extracts from the BAP31 knockdown cells (lane 3), non-specific scrambled siRNA transfected cells (lane 2) and untransfected cells (lane 1). The blots were probed with BAP31 Antibody (Product # MA3-003, 1:1500 dilution) and Rabbit anti-Rat IgG (H+L) Secondary Antibody, HRP conjugate ( Product # PA1-29927, 0.25µg/mL, 1:4000 dilution). Densitometric analysis of this western blot is shown in histogram (Fig b). Decrease in signal upon siRNA mediated knock down confirms that antibody is specific to BAP31.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunohistochemical staining of BAP31 in baboon pituitary gland using Product # MA3-003.