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- Antibody Data
- Antigen structure
- References [5]
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- Validations
- Western blot [1]
- Immunohistochemistry [2]
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- Product number
- 14487-1-AP - Provider product page
- Provider
- Proteintech Group
- Proper citation
- Proteintech Cat#14487-1-AP, RRID:AB_2165820
- Product name
- PNPT1 antibody
- Antibody type
- Polyclonal
- Description
- KD/KO validated PNPT1 antibody (Cat. #14487-1-AP) is a rabbit polyclonal antibody that shows reactivity with human, mouse, rat and has been validated for the following applications: IF, IHC, IP, WB,ELISA.
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 20ul, 150ul
Submitted references Differences in Calcium Clearance at Inner Hair Cell Active Zones May Underlie the Difference in Susceptibility to Noise-Induced Cochlea Synaptopathy of C57BL/6J and CBA/CaJ Mice.
RNA binding protein FXR1-miR301a-3p axis contributes to p21WAF1 degradation in oral cancer.
CLPP coordinates mitoribosomal assembly through the regulation of ERAL1 levels.
EF-hand protein Ca2+ buffers regulate Ca2+ influx and exocytosis in sensory hair cells.
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.
Liu H, Peng H, Wang L, Xu P, Wang Z, Liu H, Wu H
Frontiers in cell and developmental biology 2020;8:635201
Frontiers in cell and developmental biology 2020;8:635201
RNA binding protein FXR1-miR301a-3p axis contributes to p21WAF1 degradation in oral cancer.
Majumder M, Palanisamy V
PLoS genetics 2020 Jan;16(1):e1008580
PLoS genetics 2020 Jan;16(1):e1008580
CLPP coordinates mitoribosomal assembly through the regulation of ERAL1 levels.
Szczepanowska K, Maiti P, Kukat A, Hofsetz E, Nolte H, Senft K, Becker C, Ruzzenente B, Hornig-Do HT, Wibom R, Wiesner RJ, Krüger M, Trifunovic A
The EMBO journal 2016 Dec 1;35(23):2566-2583
The EMBO journal 2016 Dec 1;35(23):2566-2583
EF-hand protein Ca2+ buffers regulate Ca2+ influx and exocytosis in sensory hair cells.
Pangršič T, Gabrielaitis M, Michanski S, Schwaller B, Wolf F, Strenzke N, Moser T
Proceedings of the National Academy of Sciences of the United States of America 2015 Mar 3;112(9):E1028-37
Proceedings of the National Academy of Sciences of the United States of America 2015 Mar 3;112(9):E1028-37
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.
von Ameln S, Wang G, Boulouiz R, Rutherford MA, Smith GM, Li Y, Pogoda HM, Nürnberg G, Stiller B, Volk AE, Borck G, Hong JS, Goodyear RJ, Abidi O, Nürnberg P, Hofmann K, Richardson GP, Hammerschmidt M, Moser T, Wollnik B, Koehler CM, Teitell MA, Barakat A, Kubisch C
American journal of human genetics 2012 Nov 2;91(5):919-27
American journal of human genetics 2012 Nov 2;91(5):919-27
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Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- human brain tissue were subjected to SDS PAGE followed by western blot with 14487-1-AP(PNPT1 antibody) at dilution of 1:1500
- Sample type
- tissue
Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- Immunohistochemical of paraffin-embedded human gliomas using 14487-1-AP(PNPT1 antibody) at dilution of 1:100 (under 10x lens)
- Sample type
- tissue
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- The PNPT1 antibody from Proteintech is a rabbit polyclonal antibody to a recombinant protein of human PNPT1. This antibody recognizes human, mouse, rat antigen. The PNPT1 antibody has been validated for the following applications: ELISA, WB, IHC analysis.
