Explore
Validate
Learn
Western blot
ELISAAntibody data
- Antibody Data
- Antigen structure
- References [8]
- Comments [0]
- Validations
- Western blot [1]
- Immunohistochemistry [1]
Submit
Validation data
Reference
Comment
Report error
- Product number
- 10731-1-AP - Provider product page
- Provider
- Proteintech Group
- Proper citation
- Proteintech Cat#10731-1-AP, RRID:AB_2297956
- Product name
- MYOT antibody
- Antibody type
- Polyclonal
- Description
- MYOT antibody (Cat. #10731-1-AP) is a rabbit polyclonal antibody that shows reactivity with human, mouse, rat and has been validated for the following applications: IHC, WB, ELISA.
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 20ul, 150ul
Submitted references Modulation of Titin and Contraction-Regulating Proteins in a Rat Model of Heart Failure with Preserved Ejection Fraction: Limb vs. Diaphragmatic Muscle.
Clinicopathologic Profiles of Sporadic Late-Onset Nemaline Myopathy: Practical Importance of Anti-α-Actinin Immunostaining.
Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy.
Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations.
Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression.
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families.
Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy.
In vivo characterization of mutant myotilins.
Vahle B, Heilmann L, Schauer A, Augstein A, Jarabo MP, Barthel P, Mangner N, Labeit S, Bowen TS, Linke A, Adams V
International journal of molecular sciences 2024 Jun 16;25(12)
International journal of molecular sciences 2024 Jun 16;25(12)
Clinicopathologic Profiles of Sporadic Late-Onset Nemaline Myopathy: Practical Importance of Anti-α-Actinin Immunostaining.
Zhao B, Dai T, Zhao D, Ma X, Zhao C, Li L, Sun Y, Zhang Y, Yan Y, Lu JQ, Liu F, Yan C
Neurology(R) neuroimmunology & neuroinflammation 2022 Jul;9(4)
Neurology(R) neuroimmunology & neuroinflammation 2022 Jul;9(4)
Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy.
Yoshioka N, Kurose M, Yano M, Tran DM, Okuda S, Mori-Ochiai Y, Horie M, Nagai T, Nishino I, Shibata S, Takebayashi H
eLife 2022 Aug 9;11
eLife 2022 Aug 9;11
Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations.
Savarese M, Palmio J, Poza JJ, Weinberg J, Olive M, Cobo AM, Vihola A, Jonson PH, Sarparanta J, García-Bragado F, Urtizberea JA, Hackman P, Udd B
Annals of neurology 2019 Jun;85(6):899-906
Annals of neurology 2019 Jun;85(6):899-906
Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression.
Vihola A, Palmio J, Danielsson O, Penttilä S, Louiselle D, Pittman S, Weihl C, Udd B
Neurology. Genetics 2019 Jun;5(3):e337
Neurology. Genetics 2019 Jun;5(3):e337
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families.
Jonson PH, Palmio J, Johari M, Penttilä S, Evilä A, Nelson I, Bonne G, Wiart N, Meyer V, Boland A, Deleuze JF, Masson C, Stojkovic T, Chapon F, Romero NB, Solé G, Ferrer X, Ferreiro A, Hackman P, Richard I, Udd B
European journal of neurology 2018 May;25(5):790-794
European journal of neurology 2018 May;25(5):790-794
Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy.
Ghaoui R, Palmio J, Brewer J, Lek M, Needham M, Evilä A, Hackman P, Jonson PH, Penttilä S, Vihola A, Huovinen S, Lindfors M, Davis RL, Waddell L, Kaur S, Yiannikas C, North K, Clarke N, MacArthur DG, Sue CM, Udd B
Neurology 2016 Jan 26;86(4):391-8
Neurology 2016 Jan 26;86(4):391-8
In vivo characterization of mutant myotilins.
Keduka E, Hayashi YK, Shalaby S, Mitsuhashi H, Noguchi S, Nonaka I, Nishino I
The American journal of pathology 2012 Apr;180(4):1570-80
The American journal of pathology 2012 Apr;180(4):1570-80
No comments: Submit comment
Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- mouse skeletal muscle tissue were subjected to SDS PAGE followed by western blot with 10731-1-AP(MYOT antibody) at dilution of 1:300
- Sample type
- tissue
Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- The MYOT antibody from Proteintech is a rabbit polyclonal antibody to a recombinant protein of human MYOT. This antibody recognizes human, mouse, rat antigen. The MYOT antibody has been validated for the following applications: ELISA, WB, IHC analysis.
