KCNT1 antibody (AA 980-1060)
Quick Overview for KCNT1 antibody (AA 980-1060) (ABIN7223804)
Target
See all KCNT1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 980-1060
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Purpose
- KCNT1 Polyclonal Antibody
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Specificity
- KCNT1 Polyclonal Antibody detects endogenous levels of KCNT1 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the C-terminal region of human KCNT1 at AA range: 980-1060
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:10000). Not yet tested in other applications.
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- KCNT1 (Potassium Channel, Subfamily T, Member 1 (KCNT1))
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Alternative Name
- KCNT1
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Background
- Rabbit Anti-KCNT1 Polyclonal Antibody,KCNT1, KIAA1422, Potassium channel subfamily T member 1, KCa4.1,Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. KCNT1 (potassium sodium-activated channel subfamily T member 1) encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in KCNT1 cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants.,Potassium channel subfamily T member 1
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Molecular Weight
- observerd band 140kDa
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Gene ID
- 57582
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UniProt
- Q5JUK3
Target
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