KCNE1-Like antibody (Middle Region)
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- Target See all KCNE1-Like (KCNE1L) Antibodies
- KCNE1-Like (KCNE1L)
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Binding Specificity
- AA 74-104, Middle Region
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This KCNE1-Like antibody is un-conjugated
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Application
- Western Blotting (WB), Enzyme Immunoassay (EIA)
- Specificity
- This antibody recognizes Human KCE1L (Center).
- Purification
- Protein A column, followed by peptide affinity purification
- Immunogen
- KLH conjugated synthetic peptide between 74~104 amino acids from the Central region of Human KCE1L
- Isotype
- Ig Fraction
- Top Product
- Discover our top product KCNE1L Primary Antibody
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- Application Notes
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.25 mg/mL
- Buffer
- PBS containing 0.09 % (W/V) Sodium Azide as preservative
- Preservative
- Sodium azide
- Precaution of Use
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handling Advice
- Avoid repeated freezing and thawing.
- Storage
- 4 °C/-20 °C
- Storage Comment
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Target
- KCNE1-Like (KCNE1L)
- Alternative Name
- KCNE1L (KCNE1L Products)
- Background
- Voltage-gated potassium (Kv) 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. This gene encodes a membrane protein which has sequence similarity to the KCNE1 gene product, a member of the potassium channel, voltage-gated, isk-related subfamily. This intronless gene is deleted in AMME contiguous gene syndrome and may be involved in the cardiac and neurologic abnormalities found in the AMME contiguous gene syndrome.Synonyms: AMME syndrome candidate gene 2 protein, AMMECR2 protein, Potassium voltage-gated channel subfamily E member 1-like protein
- Molecular Weight
- 14993 Da
- Gene ID
- 23630
- NCBI Accession
- NP_036414
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