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product information
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| background |
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MTP4 protein is involved in maintaining zinc homeostasis by sequestration of excess zinc in the cytoplasm into vacuole. Alternative name: AtMTPb |
| immunogen |
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KLH-conjugated synthetic peptide derived from Arabidopsis thaliana Q6DBM8
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| antibody format |
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| quantity |
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| storage |
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store at -20°C; make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tubes. |
| tested applications |
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ELISA (ELISA), western blot (WB) |
| related products |
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collection of antibodies to tonoplast proteins AS09 485 | anti-AtMTP1 | vacuolar Zn2+/H+ antiporter
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| additional information |
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0.1 % sodium azide is added as preservative. For antibody re-suspending information check the tube lable. Antibodies will detect target protein in a few µg of a crude preparation loaded per well. If purified preparations of vacuolar and plasma membranes are used, one µg load per well should be sufficient. Protocol for isolation of vacuolar membranes can be found here. |
application information
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| recommended dilution |
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1: 8000 (ELISA), 1: 2000 with standard ECL (WB) |
| expected | apparent MW |
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42.3 | 43 kDa (Arabidopsis thaliana) |
| confirmed reactivity |
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Arabidopsis thaliana |
| predicted reactivity |
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dicots including: Capsella rubella |
| not reactive in |
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no confirmed exceptions from predicted reactivity known in the moment |
| additional information |
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Protein or membrane sample should be treated at 70°C for 10 min before loading on the gel. Diluted antibody solution can be used 2 to 3 times within one month if it contains 0.1 % sodium azide as preservative and is stored at -20ºC to -80ºC. |
| selected references |
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to be added when available |
| application example 5 µg of crude membrane fraction from Arabidopsis thaliana incubated with peptide used to elicit anti-AtMTP4 antibodies (1), 5 µg of crude membrane fraction from Arabidopsis thaliana (2), His tag recombinant MTP4 protein (3), were separated on 12 % SDS-PAGE and blotted 1h to PVDF membrane (40 min. at 10 V using BioRad semidry transfer). Filters were blocked 1h with 5 % low-fat milk powder in TBS-T (0.05% Triton X.100). Membranes were washed 5 times with TBS-T, each time in a fresh polystyrene box and probed with anti-AJ011604 | nitrate transporter antibodies (AS09 474 1:1000, 1h) and secondary anti-rabbit (1:2000, 1 h). All steps were performed in RT with agitation. |  |
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