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C57BL/6JCya-Oprm1em1flox/Cya 条件性基因敲除小鼠
产品名称:
Oprm1-flox
产品编号:
S-CKO-04120
品系背景:
C57BL/6JCya
小鼠资源库
* 使用本品系发表的文献需注明:Oprm1-flox mice (Strain S-CKO-04120) were purchased from Cyagen.
交付类型
周龄
性别
基因型
数量
基本信息
品系名称
C57BL/6JCya-Oprm1em1flox/Cya
品系编号
CKOCMP-18390-Oprm1-B6J-VA
产品编号
S-CKO-04120
基因名
Oprm1
小鼠表型
基因别称
mor,Oprm,muOR,MOP-R,MOR-1,M-OR-1,MOR-1O
品系背景
C57BL/6JCya
修饰方式
条件性基因敲除
品系描述
Oprm1位于小鼠的10号染色体,采用基因编辑技术,通过高通量电转受精卵方式,获得Oprm1基因条件性敲除小鼠,性成熟后取精子冻存。
相关疾病:
Substance Dependence
Drug Dependence
Neonatal Abstinence Syndrome
Withdrawal Disorder
Opiate Dependence
Morphine Dependence
Heroin Dependence
Pain Agnosia
Alcohol Dependence
Opioid Abuse
Cocaine Dependence
Ileus
Agnosia
Familial Hemiplegic Migraine
Specific Developmental Disorder
Alcohol Use Disorder
Eating Disorder
Major Depressive Disorder
Tobacco Addiction
Speech and Communication Disorders
Migraine with Aura
Arthritis
Temporal Lobe Epilepsy
Barbiturate Abuse
Hepatic Encephalopathy
Substance Abuse
Somatoform Disorder
Osteogenesis Imperfecta, Type Xi
Bowel Dysfunction
Anxiety
Pathological Gambling
Pain Disorder
Amnestic Disorder
Cocaine Abuse
Complex Regional Pain Syndrome
Mucopolysaccharidosis, Type Iva
Impulse Control Disorder
Fallopian Tube Clear Cell Adenocarcinoma
Mucopolysaccharidosis Iv
Myasthenic Syndrome, Congenital, 3a, Slow-Channel
Motion Sickness
Epilepsy, Idiopathic Generalized
Childhood Absence Epilepsy
Disease of Mental Health
Trigeminal Nerve Disease
Psychotic Disorder
Mucocele of Appendix
Schizophrenia
Lung Mixed Small Cell and Squamous Cell Carcinoma
Type 2 Diabetes Mellitus
Autism
Migraine with or Without Aura 1
Attention Deficit-Hyperactivity Disorder
Alzheimer Disease, Familial, 1
Peripheral Nervous System Disease
质控标准
精子检测
① 冷冻前验证精子活力观察
② 冷冻验证每批次进行复苏验证
品系状态
在研小鼠
环境标准
SPF
供应地区
全球范围