Antibody data
- Antibody Data
- Antigen structure
- References [1]
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- Validations
- Other assay [1]
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- Product number
- PA5-97143 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- PLK3 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Recombinant full-length protein
- Description
- Immunogen sequence: VLFNDGTHMA LSANRKTVHY NPTSTKHFSF SVGAVPRALQ PQLGILRYFA SYMEQHLMKG GDLPSVEEVE VPAPPLLLQW VKTDQALLML FSDGTVQVNF YGDHTKLILS GWEPLLVTFV ARNRSACTYL ASHLRQLGCS PDLRQRLRYA LRLLRDRSPA; Positive Samples: A-549, HT-1080, SKOV3, 293T, U2OS, Mouse liver, Rat liver; Cellular Location: Cytoplasm, Golgi apparatus, Nucleus, centrosome, cytoskeleton, microtubule organizing center, nucleolus
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µL
- Concentration
- 0.5 mg/mL
- Storage
- -20° C, Avoid Freeze/Thaw Cycles
Submitted references Natural COA water inhibits mitochondrial ROS-mediated apoptosis through Plk3 downregulation under STZ diabetic stress in pancreatic β-cell lines.
Lee J, Chung JO, Park SY, Rajamohan N, Singh A, Kim J, Lowe VJ, Lee S
Biochemistry and biophysics reports 2022 Jul;30:101247
Biochemistry and biophysics reports 2022 Jul;30:101247
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Supportive validation
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- Invitrogen Antibodies (provider)
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- Experimental details
- The mitochondria-mediated apoptotic cell death via streptozotocin (STZ) in beta cells is inhibited by natural COA water. (A) Beta TC-6 islet cells were cultured in a medium prepared with general water (Control) or natural COA water and then treated with streptozotocin for 72 h. Cell lysates were analyzed by immunoblotting with the antibodies indicated. (B) Beta TC-6 cells were cultured in a medium prepared with general water (Control) or natural COA water and then treated by H 2 O 2 (10 muM) for 24 h. Cell lysates were analyzed by immunoblotting with the antibodies indicated. (C) Pancreatic Beta TC-6 islet cells were cultured with indicated waters and then treated by Streptozotocin or NAC (1 mM). Cell lysates were analyzed by immunoblotting with the antibodies indicated. (D) Beta TC-6 cells were cultured in a medium prepared with general water or natural COA water and then treated with streptozotocin for 72 h. And some of these cells were treated with MG132 (10 muM, for 4 h) in a medium prepared with natural COA water. Cell lysates were analyzed by immunoblotting with the antibodies indicated. (E, F) Beta TC-6 cells were cultured in a medium prepared with general water (Control) or natural COA water and then treated with streptozotocin for 18 h. The cells were stained with MitoSOX (5 muM) for 30 min and then observed by fluorescence microscopy. Representative images of mitochondrial ROS in the Beta TC-6 cells (E). Quantification of cleaved Caspase-9, cleaved Caspase-3, cleave