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Rabbit
Anti-Kir2.1/Gold
Cat. Number:
bs-17067R-Gold
Quantity size:
100ul
35nm
Concentration:
0.4mg/ml Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Background:
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. [provided by RefSeq, Jul 2008]
Also known as:
Cardiac inward rectifier potassium channel;
HHBIRK 1;
HHBIRK1;
HHIRK1;
HIRK 1;
hIRK1;
Inward rectifier K;
inwardly rectifying subfamily J member 2;
IRK 1; IRK2_HUMAN;
IRK1;
KCNJ2;
KIR2.1;
LQT7;
Potassium channel;
Potassium channel inwardly rectifying subfamily J member 2;
Potassium inwardly rectifying channel J2;
Potassium inwardly rectifying channel subfamily J member 2;
SQT 3;
SQT3.
Specificity:
●
Rabbit Polyclonal IgG, affinity purified by Protein A.
●
Reacts with:
(predicted: )
●
Immunogen: KLH conjugated synthetic peptide derived from human Kir2.1.
●
Predicted Molecular Weight: 48kDa.
Storage:
0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300. Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
Application:
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.