Antibody data
- Antibody Data
- Antigen structure
- References [4]
- Comments [0]
- Validations [0]
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- Product number
- ABIN350148 - Provider product page
- Provider
- antibodies-online
- Proper citation
- Antibodies-Online Cat#ABIN350148, RRID:AB_10782499
- Product name
- anti-Calcium Channel, Voltage-Dependent, L Type, alpha 1S Subunit (CACNA1S) (N-Term) antibody
- Antibody type
- Polyclonal
- Antigen
- A synthetic peptide from n-terminal of human CACNA1S (Cav1.1) conjugated to an immunogenic carrier protein was used as the antigen. The peptide is homologous in rat and mouse.
- Description
- Whole serum
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Epitope
- N-Term
- Vial size
- 100 μL
- Storage
- Maintain the lyophilised/reconstituted antibodies frozen at -20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting, glycerol (1:1) may be added for an additional stability. Avoid freeze and thaw cycles.
- Handling
- Avoid freeze and thaw cycles.
Submitted references Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis.
Hypokalaemic periodic paralysis due to the CACNA1S R1239H mutation in a large African family.
Cloning of the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3).
A calcium channel mutation causing hypokalemic periodic paralysis.
Matthews E, Labrum R, Sweeney MG, Sud R, Haworth A, Chinnery PF, Meola G, Schorge S, Kullmann DM, Davis MB, Hanna MG
Neurology 2009 May 5;72(18):1544-7
Neurology 2009 May 5;72(18):1544-7
Hypokalaemic periodic paralysis due to the CACNA1S R1239H mutation in a large African family.
Houinato D, Laleye A, Adjien C, Adjagba M, Sternberg D, Hilbert P, Vallat JM, Darboux RB, Funalot B, Avode DG
Neuromuscular disorders : NMD 2007 May;17(5):419-22
Neuromuscular disorders : NMD 2007 May;17(5):419-22
Cloning of the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3).
Hogan K, Powers PA, Gregg RG
Genomics 1994 Dec;24(3):608-9
Genomics 1994 Dec;24(3):608-9
A calcium channel mutation causing hypokalemic periodic paralysis.
Jurkat-Rott K, Lehmann-Horn F, Elbaz A, Heine R, Gregg RG, Hogan K, Powers PA, Lapie P, Vale-Santos JE, Weissenbach J
Human molecular genetics 1994 Aug;3(8):1415-9
Human molecular genetics 1994 Aug;3(8):1415-9
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