Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2) (AA 41-64) antibody

Details for Product No. ABIN361769
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Antigen
Synonyms ATFB9, HHBIRK1, HHIRK1, IRK1, KIR2.1, LQT7, SQT3, Kcnf1, Kir2.1, KCNJ2, IRK-1
Epitope
AA 41-64
(8), (8), (4), (2), (1), (1), (1), (1), (1), (1), (1)
Reactivity
Human, Rat (Rattus)
(32), (17), (16), (2)
Host
Mouse
(23), (7), (6), (1)
Clonality (Clone)
Monoclonal ()
Application
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
(30), (24), (21), (3), (3), (2), (2), (2), (1), (1)
Pubmed 1 reference available
Catalog no. ABIN361769
Quantity 100 µg
Price
367.40 $   Plus shipping costs $45.00
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Immunogen Fusion protein AA 41-64 and 189-428 of mouse Kir2.1
Clone S112B-14
Isotype IgG1
Specificity Detects approx. 45 kDa.
Cross-Reactivity (Details) No cross-reactivity against Kir2.2 or Kir2.3
Sensitivity 1 µg/mL of SMC-310 was sufficient for detection of Kir2.1 in 10 µg of rat brain lysate by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody.
Purification Protein G Purified
Alternative Name Kir2.1
Background Synonyms:
HHBIRK1, HHIRK1, HIRK 1, IRK1, KCNJ2, LQT7, SQT3, potassium inwardly rectifying channel J2
The Kir2.1 inward-rectifier potassium ion channel is encoded by the KCNJ2 gene. A defect in this gene is associated with Andersen-Tawil syndrome.
Gene ID 16518
NCBI Accession NP_032451
UniProt P35561
Research Area Neurology, Ion Channels, Transporters
Application Notes Recommended Dilution: 1-10 µg/mL (WB), 0.1-1.0 µg/mL (Perox) (IHC/ICC), 1.0-10 µg/mL (IF)
Restrictions For Research Use only
Concentration 1 mg/mL
Buffer PBS pH 7.4, 50 % glycerol, 0.09 % sodium azide
Preservative Sodium azide
Storage -20 °C
Supplier Images
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2) (AA 41-64) antibody Kir2 1 Rat Brain Membranes Western Blotting.
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2) (AA 41-64) antibody (2) Kir2 Mouse backskin.
General Donaldson, Yoon, Fu et al.: "Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity." in: Annals of medicine, Vol. 36 Suppl 1, pp. 92-7, 2004 (PubMed).

Hosts (23), (7), (6), (1)
Reactivities (32), (17), (16), (2)
Applications (30), (24), (21), (3), (3), (2), (2), (2), (1), (1)
Epitopes (8), (8), (4), (2), (1), (1), (1), (1), (1), (1), (1)
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