KCNE1-Like antibody (Middle Region)

Catalog No. ABIN953001

This anti-KCNE1-Like antibody is a Rabbit Polyclonal antibody detecting KCNE1-Like in WB and EIA. Suitable for Human.

Quick Overview for KCNE1-Like antibody (Middle Region) (ABIN953001)

Target: KCNE1-Like (KCNE1L)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KCNE1-Like antibody is un-conjugated

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Product Details anti-KCNE1-Like Antibody

Binding Specificity: AA 74-104, Middle Region

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

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

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.

Target Details for KCNE1-Like

Target: KCNE1-Like (KCNE1L)

Alternative Name: KCNE1L

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