ABIN1889247
antibody from antibodies-online
Targeting: KCNQ2
BFNC, EBN, EBN1, ENB1, HNSPC, KCNA11, Kv7.2
Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations [0]
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- Product number
- ABIN1889247 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 2 (KCNQ2) (N-Term), (AA 355-372) antibody
- Antibody type
- Polyclonal
- Antigen
- A synthetic peptide corresponding to a sequence at the N-terminus of human KCNQ2(AA 355-372 DLHSTWQYYERTVTVPMY), different from the related mouse and rat sequences by one amino acid.
- Description
- Immunogen affinity purified.
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Epitope
- N-Term,AA 355-372
- Isotype
- IgG
- Vial size
- 100 μg
- Storage
- At -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for a longer time.Avoid repeated freezing and thawing.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.
A potassium channel mutation in neonatal human epilepsy.
Heron SE, Cox K, Grinton BE, Zuberi SM, Kivity S, Afawi Z, Straussberg R, Berkovic SF, Scheffer IE, Mulley JC
Journal of medical genetics 2007 Dec;44(12):791-6
Journal of medical genetics 2007 Dec;44(12):791-6
A potassium channel mutation in neonatal human epilepsy.
Biervert C, Schroeder BC, Kubisch C, Berkovic SF, Propping P, Jentsch TJ, Steinlein OK
Science (New York, N.Y.) 1998 Jan 16;279(5349):403-6
Science (New York, N.Y.) 1998 Jan 16;279(5349):403-6
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