KCNJ5 antibody (N-Term)

Catalog No. ABIN347311

This Rabbit Polyclonal antibody specifically detects KCNJ5 in WB, ELISA and IF. It exhibits reactivity toward Human, Rat and Mouse.

Quick Overview for KCNJ5 antibody (N-Term) (ABIN347311)

Target: KCNJ5 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 5 (KCNJ5))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KCNJ5 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF)

Product Details anti-KCNJ5 Antibody

Binding Specificity: N-Term

Specificity: Reacts with human GIRK4 protein

Cross-Reactivity: Mouse (Murine), Rat (Rattus)

Cross-Reactivity (Details): Cross reacts with protein from mouse, rat and other species due to sequence homology.

Purification: Antiserum

Immunogen: Synthetic peptide derived from the N-term domain of the GIRK4 protein

Isotype: IgG

Application Details

Application Notes:

Working dilution: Optimal dilution should be determined by the end user.
The following are guidelines only :
IF(1:200 - 1:1000) WB(1:1000 - 1:5000)

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Must be reconstituted in distilled water.

Storage: 4 °C/-20 °C

Storage Comment: Lyophilized powder stable for a minimum of 2 years at -20°C. Store reconstituted antibodies at +4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt.

Expiry Date: 24 months

Target Details for KCNJ5

Target: KCNJ5 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 5 (KCNJ5))

Alternative Name: G Protein-Activated Inward Rectifier Potassium Channel 4 (GIRK-4)

Background: Belongs to the inward rectifier-type potassium channel family. KCNJ5 subfamily. Defects in KCNJ5 are the cause of long QT syndrome type 13 (LQT13) and familial hyperaldosteronism type 3 (FH3).

Gene ID: 3762

UniProt: P48544

Pathways: Notch Signaling