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- References [6]
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- Product number
- ABIN955037 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Syntaxin 1A (Brain) (STX1A) (AA 36-65), (N-Term) antibody
- Antibody type
- Polyclonal
- Description
- Affinity Chromatography on Protein A
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- AA 36-65, N-Term
- Vial size
- 0.4 mL
- Storage
- Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Contribution of syntaxin 1A to the genetic susceptibility to migraine: a case-control association study in the Spanish population.
Homology with vesicle fusion mediator syntaxin-1a predicts determinants of epimorphin/syntaxin-2 function in mammary epithelial morphogenesis.
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.
Direct interaction of otoferlin with syntaxin 1A, SNAP-25, and the L-type voltage-gated calcium channel Cav1.3.
Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.
Ca2+-dependent phosphorylation of syntaxin-1A by the death-associated protein (DAP) kinase regulates its interaction with Munc18.
Corominas R, Ribasés M, Cuenca-León E, Narberhaus B, Serra SA, del Toro M, Roig M, Fernández-Fernández JM, Macaya A, Cormand B
Neuroscience letters 2009 May 15;455(2):105-9
Neuroscience letters 2009 May 15;455(2):105-9
Homology with vesicle fusion mediator syntaxin-1a predicts determinants of epimorphin/syntaxin-2 function in mammary epithelial morphogenesis.
Chen CS, Nelson CM, Khauv D, Bennett S, Radisky ES, Hirai Y, Bissell MJ, Radisky DC
The Journal of biological chemistry 2009 Mar 13;284(11):6877-84
The Journal of biological chemistry 2009 Mar 13;284(11):6877-84
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.
Hamdan FF, Piton A, Gauthier J, Lortie A, Dubeau F, Dobrzeniecka S, Spiegelman D, Noreau A, Pellerin S, Côté M, Henrion E, Fombonne E, Mottron L, Marineau C, Drapeau P, Lafrenière RG, Lacaille JC, Rouleau GA, Michaud JL
Annals of neurology 2009 Jun;65(6):748-53
Annals of neurology 2009 Jun;65(6):748-53
Direct interaction of otoferlin with syntaxin 1A, SNAP-25, and the L-type voltage-gated calcium channel Cav1.3.
Ramakrishnan NA, Drescher MJ, Drescher DG
The Journal of biological chemistry 2009 Jan 16;284(3):1364-72
The Journal of biological chemistry 2009 Jan 16;284(3):1364-72
Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.
Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Nozawa Y, Yamada Y
International journal of molecular medicine 2009 Aug;24(2):233-46
International journal of molecular medicine 2009 Aug;24(2):233-46
Ca2+-dependent phosphorylation of syntaxin-1A by the death-associated protein (DAP) kinase regulates its interaction with Munc18.
Tian JH, Das S, Sheng ZH
The Journal of biological chemistry 2003 Jul 11;278(28):26265-74
The Journal of biological chemistry 2003 Jul 11;278(28):26265-74
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