SYNE1 产品
(Spectrin Repeat Containing, Nuclear Envelope 1 (SYNE1))
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This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008].
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Featured SYNE1 Categories
SYNE1 抗体
High quality antibodies with extensive validation data.
SYNE1 ELISA试剂盒
Reliable ELISA kits for a wide range of species.
Recommended SYNE1 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, IHC, IF
Validations
- (5)
Cat. No.
ABIN7270520
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human, Mouse, Rabbit, Rat
Application
WB, ICC, IF
Validations
- (1)
Cat. No.
ABIN1042627
Quantity
0.1 mL
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA
Validations
- (1)
Cat. No.
ABIN525104
Quantity
100 μg
Datasheet
Datasheet
Recommended SYNE1 ELISA试剂盒
Product
Reactivity
Analytical Method
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Cat. No.
Quantity
Datasheet
Reactivity
Human
Analytical Method
Quantitative Sandwich ELISA
Validations
- (1)
Cat. No.
ABIN6959659
Quantity
96 tests
Datasheet
Datasheet
Reactivity
Human
Analytical Method
Quantitative Sandwich ELISA
Validations
Cat. No.
ABIN5657230
Quantity
96 tests
Datasheet
Datasheet
Recommended SYNE1 蛋白
Latest Publications for our SYNE1 Products
: "Mammalian sperm head formation involves different polarization of two novel LINC complexes." in: PLoS ONE, Vol. 5, Issue 8, pp. e12072, (2010) (PubMed).: "Direct observation of molecular arrays in the organized smooth endoplasmic reticulum." in: BMC cell biology, Vol. 10, pp. 59, (2009) (PubMed).
: "Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeleton." in: Journal of cell science, Vol. 122, Issue Pt 15, pp. 2716-26, (2009) (PubMed).
: "Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia." in: Nature genetics, Vol. 39, Issue 1, pp. 80-5, (2006) (PubMed).
Synonyms and alternative names related to SYNE1
spectrin repeat containing nuclear envelope protein 1 (SYNE1), spectrin repeat containing, nuclear envelope 1 (Syne1), spectrin repeat containing, nuclear envelope 1 (SYNE1), spectrin repeat containing, nuclear envelope 1 (syne1), spectrin repeat containing nuclear envelope protein 1 (syne1), spectrin repeat containing nuclear envelope protein 1 (Syne1), 8B, A330049M09Rik, ARCA1, BE692247, C6orf98, C130039F11Rik, CPG2, dJ45H2.2, EDMD4, MGC160118, mKIAA1756, Myne-1, MYNE1, Myne1, Nesp1, SCAR8, SYNE1Protein level used designations for SYNE1
- enaptin
- myocyte nuclear envelope protein 1
- nesprin 1
- nesprin-1
- nuclear envelope spectrin repeat-1
- synaptic nuclear envelope protein 1
- synaptic nuclei expressed gene 1
- enaptin165
- myne-1
- nuclear envelope spectrin repeat protein 1
- synaptic nuclear envelope 1
- spectrin repeat containing, nuclear envelope 1
- chromosome 6 open reading frame 98
- nesprin-1-like
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