Explore
Validate
Learn
Western blotAntibody data
- Antibody Data
- Antigen structure
- References [8]
- Comments [0]
- Validations [0]
Submit
Validation data
Reference
Comment
Report error
- Product number
- ABIN108540 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Gem (Nuclear Organelle) Associated Protein 2 (GEMIN2) (AA 12-280) antibody
- Antibody type
- Monoclonal
- Description
- Protein A
- Reactivity
- Human, Mouse, Xenopus
- Host
- Mouse
- Epitope
- AA 12-280
- Isotype
- IgG
- Antibody clone number
- 2E17
- Vial size
- 0.1 mL
- Storage
- 4°C
Submitted references A novel function for the survival motoneuron protein as a translational regulator.
Proteomic assessment of a cell model of spinal muscular atrophy.
GEMIN2 promotes accumulation of RAD51 at double-strand breaks in homologous recombination.
Regulation of SMN protein stability.
SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain.
A novel cell response triggered by interphase centromere structural instability.
Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cells.
The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins.
Sanchez G, Dury AY, Murray LM, Biondi O, Tadesse H, El Fatimy R, Kothary R, Charbonnier F, Khandjian EW, Côté J
Human molecular genetics 2013 Feb 15;22(4):668-84
Human molecular genetics 2013 Feb 15;22(4):668-84
Proteomic assessment of a cell model of spinal muscular atrophy.
Wu CY, Whye D, Glazewski L, Choe L, Kerr D, Lee KH, Mason RW, Wang W
BMC neuroscience 2011 Mar 8;12:25
BMC neuroscience 2011 Mar 8;12:25
GEMIN2 promotes accumulation of RAD51 at double-strand breaks in homologous recombination.
Takizawa Y, Qing Y, Takaku M, Ishida T, Morozumi Y, Tsujita T, Kogame T, Hirota K, Takahashi M, Shibata T, Kurumizaka H, Takeda S
Nucleic acids research 2010 Aug;38(15):5059-74
Nucleic acids research 2010 Aug;38(15):5059-74
Regulation of SMN protein stability.
Burnett BG, Muñoz E, Tandon A, Kwon DY, Sumner CJ, Fischbeck KH
Molecular and cellular biology 2009 Mar;29(5):1107-15
Molecular and cellular biology 2009 Mar;29(5):1107-15
SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain.
Walker MP, Rajendra TK, Saieva L, Fuentes JL, Pellizzoni L, Matera AG
Human molecular genetics 2008 Nov 1;17(21):3399-410
Human molecular genetics 2008 Nov 1;17(21):3399-410
A novel cell response triggered by interphase centromere structural instability.
Morency E, Sabra M, Catez F, Texier P, Lomonte P
The Journal of cell biology 2007 Jun 4;177(5):757-68
The Journal of cell biology 2007 Jun 4;177(5):757-68
Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cells.
Renvoisé B, Khoobarry K, Gendron MC, Cibert C, Viollet L, Lefebvre S
Journal of cell science 2006 Feb 15;119(Pt 4):680-92
Journal of cell science 2006 Feb 15;119(Pt 4):680-92
The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins.
Liu Q, Fischer U, Wang F, Dreyfuss G
Cell 1997 Sep 19;90(6):1013-21
Cell 1997 Sep 19;90(6):1013-21
No comments: Submit comment
No validations: Submit validation data