智鼠故事 
Cd68-P2A-iCre
复苏/繁育服务
产品名称：
Cd68-P2A-iCre
产品编号：
I001172
品系背景：
C57BL/6JCya
表达组织/细胞举例：
单核细胞、巨噬细胞
* 使用本品系发表的文献需注明：Cd68-P2A-iCre mice (Catalog I001172) were purchased from Cyagen.
交付类型
周龄
性别
基因型
数量
只
品系描述
通过基因编辑技术将P2A-iCre-WPRE-BGHpA基因表达元件整合到小鼠内源Cd68基因的终止密码子（TGA）处，即在小鼠Cd68基因调控元件的驱动下表达Cre重组酶，且不会影响小鼠内源Cd68基因的表达。
相关疾病：
Granular Cell Tumor
Histiocytic Sarcoma
Malignant Fibrous Histiocytoma
Multicentric Reticulohistiocytosis
Xanthogranulomatous Pyelonephritis
Congenital Granular Cell Tumor
Balloon Cell Malignant Melanoma
Verruciform Xanthoma of Skin
Malignant Inflammatory Fibrous Histiocytoma
Follicular Dendritic Cell Sarcoma
Neuroma
Synovitis
Axillary Lipoma
Myoblastoma
Epulis
Granulomatous Dermatitis
Congenital Epulis
Connective Tissue Benign Neoplasm
Reticulosarcoma
Breast Granular Cell Tumor
Langerhans Cell Histiocytosis
Non-Langerhans-Cell Histiocytosis
Granuloma Annulare
Malignant Granular Cell Myoblastoma
Reticulohistiocytic Granuloma
Fibroma
Malignant Giant Cell Tumor of Soft Parts
Tenosynovial Giant Cell Tumor
Necrobiosis Lipoidica
Histiocytic and Dendritic Cell Cancer
Pigmented Villonodular Synovitis
Tonsillitis
Anterior Foramen Magnum Meningioma
Vulvar Granular Cell Tumor
Bone Benign Neoplasm
Bacterial Esophagitis
Cutaneous Fibrous Histiocytoma
Rhinoscleroma
Interdigitating Dendritic Cell Sarcoma
Juvenile Xanthogranuloma
Cutaneous Leiomyosarcoma
Granulomatous Gastritis
Sarcomatoid Transitional Cell Carcinoma
Glomeruloid Hemangioma
Malignant Giant Cell Tumor
Hemangioma of Spleen
Pancytopenia
Myoma
Langerhans Cell Sarcoma
Myeloid Sarcoma
Giant Cell Reparative Granuloma
Balo Concentric Sclerosis
Liposarcoma
Myocarditis
Extraosseous Osteosarcoma
Granulomatous Orchitis
Peripheral Neuropathy with Variable Spasticity, Exercise Intolerance, and Developmental Delay
Lymphoma, Hodgkin, Classic
Conjunctival Pigmentation
Temporal Arteritis
Fibrosarcoma of Bone
Nodular Tenosynovitis
Fibrous Histiocytoma
Lymphoplasmacyte-Rich Meningioma
Pleural Lipoma
Skin Sarcoma
Bone Giant Cell Tumor
Granulomatous Myositis
Cat-Scratch Disease
Pseudosarcomatous Fibromatosis
Fox-Fordyce Disease
Histiocytosis-Lymphadenopathy Plus Syndrome
Pulmonary Artery Leiomyosarcoma
Epididymal Neoplasm
Chronic Pyelonephritis
Skin Benign Neoplasm
Orchitis
Benign Giant Cell Tumor
Lung Giant Cell Carcinoma
Neurosarcoidosis
Orbital Cancer
Pancreas Sarcoma
Villonodular Synovitis
Inflammatory Myofibroblastic Tumor
Carotid Artery Disease
Granulomatous Angiitis
Verrucous Carcinoma
Cardiac Sarcoidosis
Aortic Atherosclerosis
Lymphohistiocytoid Mesothelioma
Whipple Disease
Bronchopneumonia
Mesenchymal Cell Neoplasm
Central Nervous System Vasculitis
Acute Myocarditis
Extrinsic Cardiomyopathy
Arteriolosclerosis
Bartonellosis
Pericardium Disease
Acute Proliferative Glomerulonephritis
Crescentic Glomerulonephritis
Orbital Disease
Pleomorphic Liposarcoma
Vascular Cancer
Leukoencephalopathy, Hereditary Diffuse, with Spheroids 1
Myxofibrosarcoma
Neutrophilic Dermatosis, Acute Febrile
Pericardial Effusion
Vaginal Carcinosarcoma
Dermatofibrosarcoma Protuberans
Heart Lymphoma
Chest Wall Lipoma
Frontal Convexity Meningioma
Gaucher Disease, Perinatal Lethal
Heart Leiomyosarcoma
Hypersensitivity Reaction Type Iv Disease
Lipomatosis, Familial Multiple
Neurilemmoma
Fibrolamellar Carcinoma
Esophageal Tuberculosis
Meningioma, Familial
Encephalomalacia
Lymph Node Disease
Malignant Giant Cell Tumor of the Tendon Sheath
Maxillonasal Dysplasia, Binder Type
Aortic Aneurysm, Familial Abdominal, 1
Breast Leiomyosarcoma
Urinary Tract Obstruction
Sarcoidosis 1
Frontal Sinus Benign Neoplasm
Lipoprotein Quantitative Trait Locus
Cardiomyopathy, Infantile Histiocytoid
Granulomatosis with Polyangiitis
Hypertension, Essential
Connective Tissue Disease
Skin Disease
Peripheral Nervous System Disease
Nervous System Disease
Eye Disease
Body Mass Index Quantitative Trait Locus 11
Amyotrophic Lateral Sclerosis 1
Dilated Cardiomyopathy
Leukemia, Acute Myeloid
