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- goat polyclonal IgG, 200 µg/ml
- epitope mapping at the N-terminus of KCNE3 of human origin
- recommended for detection of KCNE3 of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including equine, canine and porcine
- blocking peptide, sc-10647 P
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Informazioni ordiniCitazioni prodotti
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| Specie |
Nome del gene |
Codice del gene |
Locus cromosoma |
Isoform (mRNA) Accession # |
codice accesso proteina |
Numero d'ordine |
| Umano |
KCNE3 |
10008 |
11q13.4 |
NM_005472 |
Q9Y6H6
|
604433 |
| Mouse |
Kcne3 |
57442 |
7 E2 |
|
Q9WTW2
|
N/A |
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KCNE3 Background Information Voltage-gated K+ channels in the plasma membrane control the repolarization and the frequency of action potentials in neurons, muscles, and other excitable cells. KCNE3 (potassium voltage-gated channel, Isk-related family, member 3), also known as HYPP, potassium channel subunit beta MiRP2 or HOKPP, is a 103 amino acid single-pass type I membrane protein belonging to the potassium channel KCNE family. Expressed predominantly in kidney, KCNE3 is also found at moderate levels in small intestine and associates with a voltage-gated potassium channel complex to regulate stability and gating kinetics. The gene encoding KCNE3 maps to human chromosome 11q13.4; defects in which are the cause of an autosomal dominant disorder known as periodic paralysis hypokalemic (or HOKPP), a muscular disorder known as thyrotoxic periodic paralysis type 1 (TTPP1) and Brugada syndrome type 6 (BRS6).
| KCNE3 (N-18) Citazioni prodotti |
Visualizza come altri ricercatori hanno utilizzato l'anticorpo KCNE3 (N-18): sc-10647 e/o i coniugati per l'anticorpo KCNE3 (N-18).
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KCNE3 (N-18)
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KCNE3 (N-18): sc-10647. Western blot analysis of KCNE3 expression in HeLa whole cell lysate.
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