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Western blotAntibody data
- Antibody Data
- Antigen structure
- References [15]
- Comments [0]
- Validations [0]
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- Product number
- HPA036985 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA036985, RRID:AB_10672785
- Product name
- Anti-GRSF1
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human GRSF1, Gene description: G-rich RNA sequence binding factor 1, Validated applications: ICC, IHC, WB, Uniprot ID: Q12849, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 100 µl
- Concentration
- 0.4 mg/ml
- Storage
- Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Handling
- The antibody solution should be gently mixed before use.
Submitted references RNA granule-clustered mitochondrial aminoacyl-tRNA synthetases form multiple complexes with the potential to fine-tune tRNA aminoacylation
Mitochondrial RNA processing defect caused by a SUPV3L1 mutation in two siblings with a novel neurodegenerative syndrome
CLPP Depletion Causes Diplotene Arrest; Underlying Testis Mitochondrial Dysfunction Occurs with Accumulation of Perrault Proteins ERAL1, PEO1, and HARS2
Male guanine-rich RNA sequence binding factor 1 knockout mice (Grsf1−/−) gain less body weight during adolescence and adulthood
Mitochondrial DNA variation in Alzheimer’s disease reveals a unique microprotein called SHMOOSE
A549 cells contain enlarged mitochondria with independently functional clustered mtDNA nucleoids
GRSF1 deficiency in skeletal muscle reduces endurance in aged mice
Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA
Mitochondrial RNA granules are fluid condensates positioned by membrane dynamics
GRSF1 is an age-related regulator of senescence
A Combined Mass Spectrometry and Data Integration Approach to Predict the Mitochondrial Poly(A) RNA Interacting Proteome
Mitochondrial RNA granules are critically dependent on mtDNA replication factors Twinkle and mtSSB
Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy
Dedicated surveillance mechanism controls G-quadruplex forming non-coding RNAs in human mitochondria
A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability
Peng G, Mao X, Cao Y, Yao S, Li Q, Chen X, Wang E, Zhou X
Nucleic Acids Research 2022;50(22):12951-12968
Nucleic Acids Research 2022;50(22):12951-12968
Mitochondrial RNA processing defect caused by a SUPV3L1 mutation in two siblings with a novel neurodegenerative syndrome
van Esveld S, Rodenburg R, Al‐Murshedi F, Al‐Ajmi E, Al‐Zuhaibi S, Huynen M, Spelbrink J
Journal of Inherited Metabolic Disease 2022;45(2):292-307
Journal of Inherited Metabolic Disease 2022;45(2):292-307
CLPP Depletion Causes Diplotene Arrest; Underlying Testis Mitochondrial Dysfunction Occurs with Accumulation of Perrault Proteins ERAL1, PEO1, and HARS2
Key J, Gispert S, Koornneef L, Sleddens-Linkels E, Kohli A, Torres-Odio S, Koepf G, Amr S, Reichlmeir M, Harter P, West A, Münch C, Baarends W, Auburger G
Cells 2022;12(1):52
Cells 2022;12(1):52
Male guanine-rich RNA sequence binding factor 1 knockout mice (Grsf1−/−) gain less body weight during adolescence and adulthood
Dumoulin B, Heydeck D, Jähn D, Lassé M, Sofi S, Ufer C, Kuhn H
Cell & Bioscience 2022;12(1)
Cell & Bioscience 2022;12(1)
Mitochondrial DNA variation in Alzheimer’s disease reveals a unique microprotein called SHMOOSE
Miller B, Kim S, Mehta H, Cao K, Kumagai H, Thumaty N, Leelaprachakul N, Braniff R, Jiao H, Vaughan J, Diedrich J, Saghatelian A, Arpawong T, Crimmins E, Ertekin-Taner N, Tubi M, Hare E, Braskie M, Décarie-Spain L, Kanoski S, Grodstein F, Bennett D, Zhao L, Toga A, Wan J, Yen K, Cohen P
Molecular Psychiatry 2022
Molecular Psychiatry 2022
A549 cells contain enlarged mitochondria with independently functional clustered mtDNA nucleoids
Metodiev M, Nasonovs A, Garcia-Diaz M, Bogenhagen D
PLOS ONE 2021;16(3):e0249047
PLOS ONE 2021;16(3):e0249047
GRSF1 deficiency in skeletal muscle reduces endurance in aged mice
Driscoll R, Krasniewski L, Cockey S, Yang J, Piao Y, Lehrmann E, Zhang Y, Michel M, Noh J, Cui C, Gorospe M
Aging 2021;13(11):14557-14570
Aging 2021;13(11):14557-14570
Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA
Key J, Torres-Odio S, Bach N, Gispert S, Koepf G, Reichlmeir M, West A, Prokisch H, Freisinger P, Newman W, Shalev S, Sieber S, Wittig I, Auburger G
Cells 2021;10(12):3354
Cells 2021;10(12):3354
Mitochondrial RNA granules are fluid condensates positioned by membrane dynamics
Rey T, Zaganelli S, Cuillery E, Vartholomaiou E, Croisier M, Martinou J, Manley S
Nature Cell Biology 2020;22(10):1180-1186
Nature Cell Biology 2020;22(10):1180-1186
GRSF1 is an age-related regulator of senescence
Kim S, Chun M, Wan J, Lee C, Yen K, Cohen P
Scientific Reports 2019;9(1)
Scientific Reports 2019;9(1)
A Combined Mass Spectrometry and Data Integration Approach to Predict the Mitochondrial Poly(A) RNA Interacting Proteome
van Esveld S, Cansız-Arda Ş, Hensen F, van der Lee R, Huynen M, Spelbrink J
Frontiers in Cell and Developmental Biology 2019;7
Frontiers in Cell and Developmental Biology 2019;7
Mitochondrial RNA granules are critically dependent on mtDNA replication factors Twinkle and mtSSB
Hensen F, Potter A, van Esveld S, Tarrés-Solé A, Chakraborty A, Solà M, Spelbrink J
Nucleic Acids Research 2019;47(7):3680-3698
Nucleic Acids Research 2019;47(7):3680-3698
Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy
Piro-Mégy C, Sarzi E, Tarrés-Solé A, Péquignot M, Hensen F, Quilès M, Manes G, Chakraborty A, Sénéchal A, Bocquet B, Cazevieille C, Roubertie A, Müller A, Charif M, Goudenège D, Lenaers G, Wilhelm H, Kellner U, Weisschuh N, Wissinger B, Zanlonghi X, Hamel C, Spelbrink J, Sola M, Delettre C
Journal of Clinical Investigation 2019;130(1):143-156
Journal of Clinical Investigation 2019;130(1):143-156
Dedicated surveillance mechanism controls G-quadruplex forming non-coding RNAs in human mitochondria
Pietras Z, Wojcik M, Borowski L, Szewczyk M, Kulinski T, Cysewski D, Stepien P, Dziembowski A, Szczesny R
Nature Communications 2018;9(1)
Nature Communications 2018;9(1)
A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability
Antonicka H, Choquet K, Lin Z, Gingras A, Kleinman C, Shoubridge E
EMBO reports 2016;18(1):28-38
EMBO reports 2016;18(1):28-38
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