kir 6.1 polyclonal antibody Search Results


90
Bioss anti kir6 1 polyclonal antibody
Expression of subunits of K ATP channels in the rat esophagus determined by RT-PCR. Homogenized samples from the rat tissues were used for RT-PCR. Amplified products of mRNA of <t>Kir6.1,</t> Kir6.2, SUR1, SUR2A and SUR2B were detected in appropriate sizes ( n =3).
Anti Kir6 1 Polyclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kir+6%2E1+polyclonal+antibody/kir+6%2E1+Polyclonal+Antibody/pmc06785617-56-42-51
Average 90 stars, based on 1 article reviews
anti kir6 1 polyclonal antibody - by Bioz Stars, 2026-10
90/100 stars
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This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

N/A
This potassium channel is controlled by G proteins. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is
  Buy from Supplier

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Expression of subunits of K ATP channels in the rat esophagus determined by RT-PCR. Homogenized samples from the rat tissues were used for RT-PCR. Amplified products of mRNA of Kir6.1, Kir6.2, SUR1, SUR2A and SUR2B were detected in appropriate sizes ( n =3).

Journal: The Journal of Veterinary Medical Science

Article Title: ATP-dependent potassium channels contribute to motor regulation of esophageal striated muscle in rats

doi: 10.1292/jvms.19-0197

Figure Lengend Snippet: Expression of subunits of K ATP channels in the rat esophagus determined by RT-PCR. Homogenized samples from the rat tissues were used for RT-PCR. Amplified products of mRNA of Kir6.1, Kir6.2, SUR1, SUR2A and SUR2B were detected in appropriate sizes ( n =3).

Article Snippet: The sections were then incubated with 2% normal goat serum at room temperature for 30 min. After rinsing in PBS, the sections were incubated with anti-SUR1 polyclonal antibody (catalog number: bs-3641R; lot number: 9B21M9; Bioss, Boston, MA, U.S.A.) diluted 1:100 or with anti-Kir6.1 polyclonal antibody (catalog number: bs-6468R; lot number: AF02227906; Bioss) diluted 1:100 at 4°C overnight.

Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction, Amplification

Histological examinations of the rat esophagus with paraffin section. (A) Kir6.1 immunoreactivity was observed mainly in the muscular layer in the rat esophagus. (B) The control staining using a normal rabbit IgG instead of antibody for K ATP channel. No specific staining was observed. L shows the lumen. Scale bar=100 µ m.

Journal: The Journal of Veterinary Medical Science

Article Title: ATP-dependent potassium channels contribute to motor regulation of esophageal striated muscle in rats

doi: 10.1292/jvms.19-0197

Figure Lengend Snippet: Histological examinations of the rat esophagus with paraffin section. (A) Kir6.1 immunoreactivity was observed mainly in the muscular layer in the rat esophagus. (B) The control staining using a normal rabbit IgG instead of antibody for K ATP channel. No specific staining was observed. L shows the lumen. Scale bar=100 µ m.

Article Snippet: The sections were then incubated with 2% normal goat serum at room temperature for 30 min. After rinsing in PBS, the sections were incubated with anti-SUR1 polyclonal antibody (catalog number: bs-3641R; lot number: 9B21M9; Bioss, Boston, MA, U.S.A.) diluted 1:100 or with anti-Kir6.1 polyclonal antibody (catalog number: bs-6468R; lot number: AF02227906; Bioss) diluted 1:100 at 4°C overnight.

Techniques: Paraffin Section, Staining

Histological examinations of the rat esophagus with cryostat section. The muscular layer of the rat esophagus showed immunoreactivity by antibodies not only for Kir6.1 (A) but also for SUR1 (B). (C) The control staining using a normal rabbit IgG instead of antibody for K ATP channel. No specific staining was observed. L shows the lumen. Scale bar=100 µ m.

Journal: The Journal of Veterinary Medical Science

Article Title: ATP-dependent potassium channels contribute to motor regulation of esophageal striated muscle in rats

doi: 10.1292/jvms.19-0197

Figure Lengend Snippet: Histological examinations of the rat esophagus with cryostat section. The muscular layer of the rat esophagus showed immunoreactivity by antibodies not only for Kir6.1 (A) but also for SUR1 (B). (C) The control staining using a normal rabbit IgG instead of antibody for K ATP channel. No specific staining was observed. L shows the lumen. Scale bar=100 µ m.

Article Snippet: The sections were then incubated with 2% normal goat serum at room temperature for 30 min. After rinsing in PBS, the sections were incubated with anti-SUR1 polyclonal antibody (catalog number: bs-3641R; lot number: 9B21M9; Bioss, Boston, MA, U.S.A.) diluted 1:100 or with anti-Kir6.1 polyclonal antibody (catalog number: bs-6468R; lot number: AF02227906; Bioss) diluted 1:100 at 4°C overnight.

Techniques: Staining