Use Able AI chat for product recommendations

Kir4.1 Monoclonal antibody, PBS Only

Kir4.1 Monoclonal Antibody for WB, Indirect ELISA

Cat No. 66931-1-PBS
Clone No. 2D6A6
Review Product
Download datasheet

Host / Isotype

Mouse / IgG1

Reactivity

human, mouse

Applications

WB, Indirect ELISA

KCNJ10, 2D6A6, ATP-dependent inwardly rectifying potassium channel Kir4.1, ATP-sensitive inward rectifier potassium channel 10, BIRK 10

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 
SKU: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:

Able AI
Able AI
What's the best dilution for Kir4.1 in ?

Product Information

66931-1-PBS targets Kir4.1 in WB, Indirect ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Immunogen

CatNo: Ag16785

Product name: Recombinant human KCNJ10 protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 224-426 aa of BC034036

Sequence: ETIRFSQHAVVASHNGKPCLMIRVANMRKSLLIGCQVTGKLLQTHQTKEGENIRLNQVNVTFQVDTASDSPFLILPLTFYHVVDETSPLKDLPLRSGEGDFELVLILSGTVESTSATCQVRTSYLPEEILWGYEFTPAISLSASGKYIADFSLFDQVVKVASPSGLRDSTVRYGDPEKLKLEESLREQAEKEGSALSVRISNV

Predict reactive species
Full Name potassium inwardly-rectifying channel, subfamily J, member 10
Calculated Molecular Weight 379 aa, 41 kDa
Observed Molecular Weight 40 kDa
GenBank Accession NumberBC034036
Gene Symbol Kir4.1
Gene ID (NCBI) 3766
RRIDAB_2882257
Conjugate Unconjugated
FormLiquid
Purification MethodProtein G purification
UNIPROT IDP78508
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

ATP-sensitive inward rectifier potassium channel 10 (KCNJ10, also known as Kir4.1) is an inwardly rectifying K⁺ channel predominantly expressed in glial cells within the central nervous system. In glial cells, Kir4.1 participates in multiple physiological processes, including the maintenance of extracellular K⁺ homeostasis, preservation of astrocyte resting membrane potential, regulation of cell volume, and promotion of glutamate uptake (PMID: 26961251). Kir4.1 can assemble into Kir4.1/Kir5.1 heteromeric channels, which mediate basolateral K⁺ recycling in renal distal tubules. This activity is essential for tubular Na⁺ reabsorption. Pathogenic mutations in Kir4.1 are associated with EAST/SeSAME syndrome, a genetic disorder marked by renal salt wasting (PMID: 24561201; 8995301).

Loading...
||
New chat

Able™

正在加载,请稍候...