Western blot shows lysates of Human heart ventricle tissue and human lung tissue. PVDF membrane was probed with 3 µg/mL of Rabbit Anti-Human/Mouse Kir2.1 Monoclonal Antibody (Catalog # MAB9548) followed by ...read more
Kir2.1 was detected in immersion fixed paraffin-embedded sections of human heart using Rabbit Anti-Human/Mouse Kir2.1 Monoclonal Antibody (Catalog # MAB9548) at 3 µg/mL for 1 hour at room temperature followed by ...read more
Kir2.1 was detected in perfusion fixed frozen sections of mouse heart using Rabbit Anti-Human/Mouse Kir2.1 Monoclonal Antibody (Catalog # MAB9548) at 3 µg/mL for 1 hour at room temperature followed by ...read more
Kir2.1 was detected in immersion fixed human cardiomyocytes using Rabbit Anti-Human/Mouse Kir2.1 Monoclonal Antibody (Catalog # MAB9548) at 2 µg/mL for 3 hours at room temperature. Cells were stained using the ...read more
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
6 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.
Reconstitution Instructions
Reconstitute at 0.5 mg/mL in sterile PBS.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Kir2.1 Antibody (2153C) [Unconjugated]
ATFB9
Cardiac inward rectifier potassium channel
HHBIRK1
HHIRK1
HIRK1
Inward rectifier K(+) channel Kir2.1
inward rectifier K+ channel KIR2.1
inward rectifier potassium channel 2
IRK1
IRK-1
IRK1LQT7
KCNJ2
Kir2.1
LQT7
Potassium channel, inwardly rectifying subfamily J member 2
potassium inwardly-rectifying channel, subfamily J, member 2
SQT3
Background
Human Inward Rectifier Potassium Channel 2 (KIR2.1), also known as KCNJ2, is a 427 amino acid (aa) integral membrane protein with 98% homology
with mouse and rat KIR2.1. This
potassium channel preferentially allows potassium to flow into the cell, which
is thought to generate action potential waveform and excitability in neuronal
and muscle tissues. Mutations in the KIR2.1 gene are associated with Andersen
syndrome, with associated paralysis, cardiac arrhythmias and dysmorphic
features. KIR2.1 is widely expressed, notably in heart, placenta, lung, skeletal
muscle, kidney and spleen. Expression of KIR2.1 is necessary for development of
mature cardiomyocytes from mouse embryonic stem cells.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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