Conventional / global / constitutive KO
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Browse 3 Sigmar1 mouse models including conditional knockout, knockout variants from ingenious targeting laboratory. Available as Sigmar1 conditional knockout mouse, Sigmar1 knockout mouse. Contact us for availability and fast turnaround.
At mitochondria-associated ER membranes, the product of mouse Sigmar1, ortholog of human SIGMAR1, functions as a ligand-operated chaperone rather than a classical receptor, forming an ER membrane protein that associates with BiP and, upon agonist binding or calcium depletion, dissociates to stabilize IP3 receptor type 3 and sustain calcium transfer from ER to mitochondria. Sigma-1 receptor also chaperones ion channels, modulates the unfolded protein response through IRE1, and translocates to the nuclear envelope and plasma membrane. Recessive E102Q causes juvenile ALS16 and other variants cause distal hereditary motor neuropathy, with loss of contact site integrity, calcium dysregulation, and impaired autophagic flux as proposed mechanisms. Because Sigmar1 knockout mice are viable with late-onset motor deficits, both conditional null and patient knockin alleles are practical, and humanization is attractive given active agonist pharmacology such as pridopidine. Select motor neuron Cre drivers when contact site integrity and neuromuscular junction endpoints matter.
ingenious targeting laboratory offers 3 distinct Sigmar1 (SIGMAR1) 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 |
|---|---|
| 3 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 Sigmar1 (human SIGMAR1). 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
3 Sigmar1 lines with QC documentation and technical support. Sigmar1 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
We have 3 Sigmar1 models available — including Conditional Knockout, Knockout types. Contact us today for current availability and our fastest turnaround options. All models come with full QC documentation and 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 Sigmar1 knockout mouse has the Sigmar1 gene permanently inactivated, enabling loss of function studies. A Sigmar1 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Sigmar1, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Sigmar1 organized by modification type. Each URL is indexable and matches common search patterns.