KCNE1-Like antibody (AA 67-96)

Catalog No. ABIN653619

The Rabbit Polyclonal anti-KCNE1-Like antibody (Clone RB24387) (ABIN653619) specifically detects KCNE1-Like in WB. The antibody is reactive with Human samples.

Quick Overview for KCNE1-Like antibody (AA 67-96) (ABIN653619)

Target: KCNE1-Like (KCNE1L)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KCNE1-Like antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB24387

Product Details anti-KCNE1-Like Antibody

Binding Specificity: AA 67-96

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This KCE1L antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 67-96 amino acids from the Central region of human KCE1L.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Expiry Date: 6 months

Target Details for KCNE1-Like

Target: KCNE1-Like (KCNE1L)

Alternative Name: KCE1L

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.

Molecular Weight: 14993

Gene ID: 23630

NCBI Accession: NP_036414

UniProt: Q9UJ90