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Hematological Research

 
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Hematological Research

Allele Symbol
 
Strain Description
Stock Number Strain Name
   (link to Data Sheet)
Ccl11tm1Mer 017618
Awaiting Transfer from the Donor
C.129S6(Cg)-Ccl11tm1Mer/J
These Ccl11 knockout mice exhibit a reduced total eosinophil count in peripheral blood and may be useful for studying eosinophilia and inflammatory disorders.
Eif2c2tm3Ghan 014150
In Progress
B6;129S6-Eif2c2tm3Ghan/J
This mutant strain lacks Eif2c2 catalytic activity and may be useful in studies of microRNA biogenesis and erythropoiesis.
Hfe2tm1Nca 017788
In Progress
129S-Hfe2tm1Nca/J
These Hfe2 knockout mice exhibit iron loading and have applications in studies of juvenile or Type2A hemochromatosis, iron homeostasis and iron-induced oxidative damage.
Hfetm2Nca 017785
In Progress
129S-Hfetm2Nca/J
These mice carry a targeted mutation of Hfe, hemochromatosis, exhibit iron loading, and have applications in studies of hereditary hemochromatosis, iron homeostasis and innate immune response
Hfetm2Nca 017784
Under Development for Cryo
B6.129S6-Hfetm2Nca/J
These mice carry a targeted mutation of Hfe, hemochromatosis, exhibit iron loading, and have applications in studies of hereditary hemochromatosis, iron homeostasis and innate immune response.
Kitltm1.1Sjm 017860
Awaiting Transfer from the Donor
STOCK Kitltm1.1Sjm/J
An EGFP reporter disrupts expression of the Kitl gene in this targeted mutation strain. EGFP is primarily expressed by perivascular endothelial and stromal cells throughout the bone marrow in heterozygotes.
Lattm6(DTR)Mal 016937
In Progress
B6.129S2-Lattm6(DTR)Mal/J
Latfl-dtr mutant mice contain a loxP site downstream from exon 1, and an internal ribosome entry site (IRES), a human diphtheria toxin receptor, and an enhanced green fluorescent protein (EGFP) followed by a second loxP site downstream of the internal stop codon of the linker for activation of T cells (Lat) gene. These mice may be useful for studying the TCR signaling cascade and T cell homeostasis.
Mll1tm2(MLLT3)Thr 009079
On Hold
STOCK Mll1tm2(MLLT3)Thr/KsyJ
Beginning around six months of age, these Mll-AF9 knock-in mice recapitulate the acute myeloid leukemia (AML) phenotype associated with the t(9;11)(p22;q23) translocation in humans and may be useful for studying hematopoietic development, cancer, and acute myeloid leukemia.
Nanogtm1Hoch 016233
Awaiting Transfer from the Donor
129S;B6-Nanogtm1Hoch/J
A GFP-IRES-puro-cassette replaces the coding region of the Nanog gene in these mice. Mouse embryonic fibroblasts containing this mutation may be useful for identifying induced pluripotent stem cells.
Sept4tm1Hs 018160
Awaiting Transfer from the Donor
129-Sept4tm1Hs/J
Septin 4 (Sept4) homozygous knockout males are sterile due to immotile and structurally defective sperm. Mice also exhibit increased incidence of hematopoietic malignancies having increased numbers of hematopoietic stem and progenitor cells (HSPCs).
Sept4tm1Hs 018159
Awaiting Transfer from the Donor
B6.129P2-Sept4tm1Hs/J
Septin 4 (Sept4) homozygous knockout males are sterile due to immotile and structurally defective sperm. Mice also exhibit increased incidence of hematopoietic malignancies having increased numbers of hematopoietic stem and progenitor cells (HSPCs).
Sept4tm1Hs 018161
Awaiting Transfer from the Donor
FVB.129P2-Sept4tm1Hs/J
Septin 4 (Sept4) homozygous knockout males are sterile due to immotile and structurally defective sperm. Mice also exhibit increased incidence of hematopoietic malignancies having increased numbers of hematopoietic stem and progenitor cells (HSPCs).
Slc11a2tm2Nca 017789
In Progress
129S-Slc11a2tm2Nca/J
These Dmt1fl mice possess loxP sites flanking exons 6-8 of the solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 (Slc11a2) gene and have applications in studies related to anemia, iron homeostasis and micronutrient and drug absorption in the intestine.
Slc40a1tm2Nca 017790
In Progress
129S-Slc40a1tm2Nca/J
These ferroportinfl mice possess loxP sites flanking exons 6 and 7 of the solute carrier family 40 (iron-regulated transporter), member 1 (Slc40a1) gene and have applications in studies related to type 4 hemochromatosis, anemia, and iron homeostasis.
Tg(CD4-Il17re)#Cdon 017943
In Progress
C57BL/6-Tg(CD4-Il17re)#Cdon/J
These mice contain a transgene utilizing a human CD4 promoter driving expression of IL-17RE in Th17 cells. They exhibit a susceptibility to EAE.
Tg(Cp-EGFP)25Gaia 005854
On Hold
STOCK Tg(Cp-EGFP)25Gaia/J
Mice homozygous for the Notch reporter transgene are viable, fertile, normal in size, and do not display any behavioral abnormalities. Enhanced green fluorescent protein (EGFP) expression is present in a wide variety of hemizygous cell/tissue types during development and in the adult, including enriched hematopoietic stem cell (HSC) populations. The location of EGFP expression is consistent with Notch signaling pathway elements/genes and appears to faithfully reflect canonical (CBF1-mediated) Notch activity. With respect to hematopoiesis, low expression is shown in fully differentiated cells of the peripheral lymphoid organs (blood and spleen). Isolated HSC retain their ability to differentiate. Mice expressing this Notch reporter transgene may be useful in studying HSC populations and other cell types utilizing the Notch, CBF1, or Wnt signaling pathways. As immature (double negative [DN]) thymocytes have differential expression patterns as they progress from DN1-DN4, these mice may al .....
For more information please see the full phenotype on the strain data sheet
Tg(H2-K-S100a9,GFP)1Gabr 018055
Awaiting Transfer from the Donor
B6.FVB-Tg(H2-K-S100a9,GFP)1Gabr/J
These transgenic mice express S100a9 (S100 calcium binding protein A9 (calgranulin B)), a myeloid-related protein, and GFP under the control of the hematopoietic cell-specific H2-K promoter. Overexpression of S100a9 inhibits the differentiation of dendritic cells and macrophages while inducing an accumulation of myeloid-derived suppressor cells.
018322
Awaiting Transfer from the Donor
STOCK Tg(Cp-EGFP)25Gaia/ReyaJ
These Notch reporter mice are useful in studying hematopoietic stem cell populations utilizing the Notch or Wnt signaling pathways, as well as in thymocyte maturation studies.

(18 stocks)

 

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