WB
Western blot analysis of kmo using anti-kmo antibody . The sample well of each lane was loaded with 30 ug of sample under reducing conditions.Lane 1: Marker,Lane 2: Zebrafish tissue lysates,Lane 3: Zebrafish head tissue lysates,Lane 4: Zebrafish body tissue lysates.After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-kmo antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody . The signal is developed using ECL Plus Western Blotting Substrate . A specific band was detected for kmo at approximately 54 kDa. The expected band size for kmo is at 54 kDa.| Product Name | Anti-Zebrafish kmo Antibody |
|---|---|
| Antibody Type | Primary Antibodies |
| Clonality | Polyclonal |
|---|---|
| Isotype | IgG |
| Host Species | Rabbit |
| Tested Applications | WB |
| WB:1:500-1:2000 |
|
| Species Reactivity | Zebrafish |
| Concentration | 500ug/ml |
| Purification | Affinity purified |
| Target | kmo |
|---|---|
| Molecular Weight(MW) | 54 kDa |
| SwissProt ID | Q1RLY6 |
|---|
WB
Western blot analysis of kmo using anti-kmo antibody . The sample well of each lane was loaded with 30 ug of sample under reducing conditions.Lane 1: Marker,Lane 2: Zebrafish tissue lysates,Lane 3: Zebrafish head tissue lysates,Lane 4: Zebrafish body tissue lysates.After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-kmo antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody . The signal is developed using ECL Plus Western Blotting Substrate . A specific band was detected for kmo at approximately 54 kDa. The expected band size for kmo is at 54 kDa.| Application Notes | WB:1:500-1:2000 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | 12 months from date of receipt,-20℃ as supplied. |
| Storage Buffer | PBS, 0.02% NaN3, 1 mg/ml BSA and 50% glycerol. |
