Anti-Slo1 Maxi-K+ Channel Antibody (BSA and Azide free) (L6/60)
Our carrier-free Anti-Slo1 maxi-K+ channel mouse monoclonal primary antibody from NeuroMab is produced in-house from hybridoma clone L6/60. It is KO validated, detects human, mouse, rat, sheep, and zebrafish Slo1 maxi-K+ channel, and is purified by Protein A chromatography. It is great for use in IHC, ICC, IP, WB.
mSlo maxi K+ channel (Calcium-activated potassium channel subunit alpha-1) is a member of BK channel alpha subunit family and has the particularity to be regulated by both Ca2+ and membrane depolarization.BK channels have a tetrameric structure. Each subunit is the product of the KCNMA1 gene. All modulatory subunits encoded by KCNMB1, KCNMB2, KCNMB3, or KCNMB4 can associate with the tetrameric channel. MSlo plays a major role in controlling cell excitability, which regulates smooth muscle contractions, transmitter release, and innate immune system cell activation. MSlo maxi-K+ channel contributes to repolarization of the membrane potential as it exports K+ out of the cytosol.
Purified by Protein A chromatography
1 mg/mL
Monoclonal
L6/60
IgG2a
ELISA, ICC, IHC, WB
Mouse
Kcnma1 Kcnma
110-130 kDa
Fusion protein amino acids 690-1196 (cytoplasmic C-terminus) of mouse Slo1 (accession number AAA39746) produced recombinantly in E. Coli
Human, Mouse, Rat, Sheep, Zebrafish
Aliquot and store at ≤ -20°C for long term storage. For short term storage, store at 2-8°C. For maximum recovery of product, centrifuge the vial prior to removing the cap.
Liquid
Produced by in vitro bioreactor culture of hybridoma line followed by Protein A affinity chromatography and buffer exchanged into 1X PBS. Purified mAbs are >90% specific antibody.
PBS
Unconjugated
No cross-reactivity reported
Each new lot of antibody is quality control tested by western blot on rat whole brain lysate and confirmed to stain the expected molecular weight band.
These antibodies are to be used as research laboratory reagents and are not for use as diagnostic or therapeutic reagents in humans.
KO Validated