Antibody data
- Antibody Data
- Antigen structure
- References [5]
- Comments [0]
- Validations
- Western blot [2]
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Validation data
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- Product number
- NB300-535 - Provider product page
- Provider
- Novus Biologicals
- Proper citation
- Novus Cat#NB300-535, RRID:AB_2131348
- Product name
- Rabbit Polyclonal Maxi Potassium channel beta Antibody
- Antibody type
- Polyclonal
- Description
- Immunogen affinity purified.
- Reactivity
- Human, Mouse, Rat, Canine, Porcine, Rabbit
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 ug
- Concentration
- 1 mg/ml
- Storage
- Store at -20C. Avoid freeze-thaw cycles.
Submitted references Activation of BK Channel Contributes to PL-Induced Mesenchymal Stem Cell Migration.
Impaired function of coronary BK(Ca) channels in metabolic syndrome.
Interleukin-4 activates large-conductance, calcium-activated potassium (BKCa) channels in human airway smooth muscle cells.
Slo1 caveolin-binding motif, a mechanism of caveolin-1-Slo1 interaction regulating Slo1 surface expression.
Somatic localization of a specific large-conductance calcium-activated potassium channel subtype controls compartmentalized ethanol sensitivity in the nucleus accumbens.
Echeverry S, Grismaldo A, Sánchez C, Sierra C, Henao JC, Granados ST, Sutachán JJ, Torres YP
Frontiers in physiology 2020;11:210
Frontiers in physiology 2020;11:210
Impaired function of coronary BK(Ca) channels in metabolic syndrome.
Borbouse L, Dick GM, Asano S, Bender SB, Dincer UD, Payne GA, Neeb ZP, Bratz IN, Sturek M, Tune JD
American journal of physiology. Heart and circulatory physiology 2009 Nov;297(5):H1629-37
American journal of physiology. Heart and circulatory physiology 2009 Nov;297(5):H1629-37
Interleukin-4 activates large-conductance, calcium-activated potassium (BKCa) channels in human airway smooth muscle cells.
Martin G, O'Connell RJ, Pietrzykowski AZ, Treistman SN, Ethier MF, Madison JM
Experimental physiology 2008 Jul;93(7):908-18
Experimental physiology 2008 Jul;93(7):908-18
Slo1 caveolin-binding motif, a mechanism of caveolin-1-Slo1 interaction regulating Slo1 surface expression.
Alioua A, Lu R, Kumar Y, Eghbali M, Kundu P, Toro L, Stefani E
The Journal of biological chemistry 2008 Feb 22;283(8):4808-17
The Journal of biological chemistry 2008 Feb 22;283(8):4808-17
Somatic localization of a specific large-conductance calcium-activated potassium channel subtype controls compartmentalized ethanol sensitivity in the nucleus accumbens.
Martin G, Puig S, Pietrzykowski A, Zadek P, Emery P, Treistman S
The Journal of neuroscience : the official journal of the Society for Neuroscience 2004 Jul 21;24(29):6563-72
The Journal of neuroscience : the official journal of the Society for Neuroscience 2004 Jul 21;24(29):6563-72
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Supportive validation
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Western Blot: Maxi Potassium channel beta Antibody [NB300-535] - Analysis of Maxi K+ Beta (KCNMB1) was performed by loading 20ug of Movas whole cell lysates with and without Maxi K+ Beta (KCNMB1) siRNA and 10ul prestained protein ladder per well onto a 4-20% Tris-Glycine polyacrylamide gel. Proteins were transferred to a nitrocellulose membrane and blocked with 5% Milk/TBST for at least 1 hour at room temperature. Maxi K+ Beta was detected using a Maxi K+ Beta rabbit polyclonal antibody at a concentration of 1ug/ml in blocking buffer overnight at 4 degrees C on a rocking platform, followed by a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5,000 for at least 1 hour at room temperature. Chemiluminescent detection was performed.
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Western Blot: Maxi Potassium channel beta Antibody [NB300-535] - Analysis of Maxi K+ Beta was performed by loading 20ug of Movas whole cell lysates and 10ul prestained protein ladder per well onto a 4-20% Tris-Glycine polyacrylamide gel. Proteins were transferred to a nitrocellulose membrane u and blocked with 5% Milk/TBST for at least 1 hour at room temperature. Maxi K+ Beta was detected using a Maxi K+ rabbit polyclonal antibody at a concentration of 1ug/ml in blocking buffer overnight at 4 degrees C on a rocking platform, followed by a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5,000 for at least 1 hour at room temperature. Chemiluminescent detection was performed.