Potassium Voltage-Gated Channel Subfamily Q Member 1 (KCNQ1) Peptide
Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
Description
Potassium Voltage-Gated Channel Subfamily Q Member 1 (KCNQ1) Peptide is a synthetic peptide.
Documents del producto
Product specifications
| Category | Proteins and Peptides |
| Immunogen Target | Potassium Voltage-Gated Channel Subfamily Q Member 1 (KCNQ1) |
| Host | Synthetic |
| Recommended Dilution | BL (predicted): 0.5 mg/ml. Optimal dilutions/concentrations should be determined by the end user. |
| Conjugation | Unconjugated |
| Observed MW | Sequence Fragment: C-Terminus: C-EQLTVPRRGPDEGS |
| Size 1 | 100 µg |
| Form | Lyophilized Reconstitute in deionized water. |
| Tested Applications | P-ELISA |
| Buffer | Prior to lyophilization: Deionized water. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| Gene ID | 3784, 16535, 84020 |
| NCBI Accession | NP_000209.2, NP_861463.1 |
| Background | Protein KCNQ1 |
| Note | This product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use. |
Descripción
Related Products
Potassium Voltage-Gated Channel Subfamily Q Member 1 (KCNQ1) Antibody
KCNQ1 Antibody is a Rabbit Polyclonal antibody against KCNQ1. KCNQ1 is a protein for a voltage-gated potassium channel required for the repolarization phase of the cardiac action potential. The gene product can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3.
Ver Producto
Potassium Voltage-Gated Channel Subfamily Q Member 1 (KCNQ1) Antibody
This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential.This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3.Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation.This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others.This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS.Alternatively spliced transcript variants have been found for this gene.
Ver Producto
Potassium Voltage-Gated Channel Subfamily Q Member 1 (KCNQ1) Antibody
This gene encodes a voltage-gated potassium channel required for the repolarization phase of the cardiac action potential. The gene product can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome and familial atrial fibrillation. The gene is located in a region of chromosome 11 that contains a number of contiguous genes, which are abnormally imprinted in cancer and the Beckwith-Wiedemann syndrome. This gene is also imprinted, with preferential expression from the maternal allele in some tissues, excluding cardiac muscle. Alternatively spliced transcripts encoding distinct isoforms have been described.
Ver Producto