Conventional / global / constitutive KO
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Browse 2 Kcnj10 mouse models including conditional knockout, knockout variants — in stock and ready to ship from ingenious targeting laboratory. Available as Kcnj10 conditional knockout mouse, Kcnj10 knockout mouse. Request a quote within 24 hours.
Kcnj10, the mouse ortholog of human KCNJ10, encodes Kir4.1, the principal inwardly rectifying potassium channel of astrocytes, Bergmann glia, oligodendrocytes, and retinal Muller cells, where it clamps the glial membrane near the potassium equilibrium potential and performs spatial buffering of extracellular potassium released during neuronal firing. Kir4.1 functions as a homotetramer or as an obligate partner in Kir4.1/Kir5.1 heteromers with the Kcnj16 product, which confers steep intracellular pH sensitivity, and it also operates in the distal convoluted tubule and stria vascularis, coupling to the sodium pump and to chloride handling. Biallelic human mutations cause SeSAME/EAST syndrome with seizures, ataxia, sensorineural deafness, and renal salt wasting, and constitutive nulls die in the early postnatal period with hypomyelination and severe motor impairment, so glia-restricted conditional deletion using Gfap-Cre or Aldh1l1-CreER is required for adult work. No other glial Kir substitutes effectively, so match allele to whether the endpoint is potassium clearance, seizure threshold, or renal electrolyte handling.
ingenious targeting laboratory offers 2 distinct Kcnj10 (KCNJ10) catalog mouse models, featuring conditional knockout and standard knockout. Researchers can order pre-developed catalog lines or request a custom mouse model, including humanized, knockin, and transgenic variations with verified germline transmission.
| Model Availability | Allele Class Options |
|---|---|
| 2 Ready Catalog Lines | Conditional Knockout (cKO) |
| Custom Model Generation | Constitutive Knockout (KO) |
| Advanced Modifications | Humanized, Knockin, Transgenic |
Knockout
Conditional knockout
Knockin
Humanized
Transgenic / overexpression
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Knockout, conditional, knockin, humanized, and related paths for Kcnj10 (human KCNJ10). Catalog lines ship when inventory exists. Everything else is a generation quote.
Specify tissue or Cre driver on quote
Convertible floxed allele pathway
Multi allele / compound knockout project
BAC scale deletion or targeting
LSL or conditional expression knockin
Domain or partial humanization scope
Checkpoint IO humanization when gene is a checkpoint target
Multi humanized / combination IO project
BAC transgenic or large fragment insert
Tamoxifen or dox inducible Cre
Dual recombinase breeding scheme
Flp or FRT derivative allele pairing
Catalog reporter lines not tied to a single gene allele
Specify rat on quote
Specify rabbit on quote
Background substrain on quote
Background strain on quote
2 Kcnj10 lines with QC documentation and technical support. Kcnj10 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
We have 2 Kcnj10 models in stock — including Conditional Knockout, Knockout types. In stock and ready to ship this week. All models come with full QC documentation, health certificates, and dedicated technical support.
Best pricing in the industry. Get a quote in 24 hours. Our team of PhD scientists is available to help you select the right model for your research.
Order catalog modelA Kcnj10 knockout mouse has the Kcnj10 gene permanently inactivated, enabling loss of function studies. A Kcnj10 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Kcnj10, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Kcnj10 organized by modification type. Each URL is indexable and matches common search patterns.