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Products by Disease or Condition

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 rightarrow MyBioSource's team have spent countless hours of research to find the most common diseases or conditions and associate them with our products.

 rightarrow  Each disease or condition is linked to the top products based on our sophisticated "P2D (Products2Disease)" indexing algorithm.

Below are the list of available diseases start with:   ALL    #    A    B    C    D    E    F    G    H    I    J    K    L    M    N    O    P    Q    R    S    T    U    V    W    X    Y    Z    
 M
    • Machado-Joseph Disease
    • Macrocephaly
    • MACROCEPHALY, ALOPECIA, CUTIS LAXA, AND SCOLIOSIS
    • Macrostomia
    • Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related
    • Macular Degeneration
    • Macular Degeneration, Age-Related, 1
    • Macular Degeneration, Age-Related, 2
    • Macular Degeneration, Age-Related, 3
    • Macular Degeneration, Age-Related, 4
    • Macular Degeneration, Age-Related, 7
    • Macular dystrophy, corneal type 1
    • MACULAR DYSTROPHY, VITELLIFORM
    • MACULAR DYSTROPHY, VITELLIFORM, ADULT-ONSET
    • Macular Edema
    • Magnesium Deficiency
    • Majeed syndrome
    • Malabsorption Syndromes
    • Malaria
    • Malaria, Falciparum
    • Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa
    • Male Urogenital Diseases
    • Malformations of Cortical Development
    • Malignant Hyperthermia
    • Malignant hyperthermia susceptibility type 1
    • Malignant hyperthermia susceptibility type 5
    • Malnutrition
    • Malonic aciduria
    • Malpuech facial clefting syndrome
    • Mammary Neoplasms, Animal
    • Mammary Neoplasms, Experimental
    • Mandibular Diseases
    • Mandibuloacral dysplasia with type B lipodystrophy
    • Mandibulofacial Dysostosis
    • Manganese Poisoning
    • Maple Syrup Urine Disease
    • Marfan Syndrome
    • Marijuana Abuse
    • MARINESCO-SJOGREN SYNDROME
    • Marles Greenberg Persaud syndrome
    • Marshall syndrome
    • Martin-Probst Deafness-Mental Retardation Syndrome
    • Martsolf syndrome
    • MASP2 Deficiency
    • Massive Hepatic Necrosis
    • MAST SYNDROME
    • MATURITY-ONSET DIABETES OF THE YOUNG
    • Maturity-Onset Diabetes of the Young, Type 2
    • Maturity-Onset Diabetes Of The Young, Type 9
    • Maxillofacial Abnormalities
    • May-Hegglin anomaly
    • MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME
    • MCCUNE-ALBRIGHT SYNDROME
    • McKusick Kaufman syndrome
    • Measles
    • Meckel syndrome type 1
    • Meckel syndrome type 3
    • Meckel Syndrome, Type 4
    • MECKEL SYNDROME, TYPE 6
    • Medium chain acyl CoA dehydrogenase deficiency
    • Medulloblastoma
    • Megacolon
    • Megacystis microcolon intestinal hypoperistalsis syndrome
    • Megalencephalic leukoencephalopathy with subcortical cysts
    • Megalencephaly
    • MEGALOBLASTIC ANEMIA 1
    • Meier-Gorlin syndrome
    • Melanoma
    • Melanoma, Amelanotic
    • MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1
    • Melanoma, Experimental
    • Melanosis
    • Melorheostosis
    • Memory Disorders
    • Meniere Disease
    • Meningeal Neoplasms
    • Meningioma
    • Meningioma, familial
    • Meningitis
    • Meningococcal Infections
    • Meningomyelocele
    • Menkes Kinky Hair Syndrome
    • Mental Disorders
    • Mental Disorders Diagnosed in Childhood
    • Mental Retardation
    • Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia
    • MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES
    • Mental Retardation, Autosomal Recessive 13
    • Mental Retardation, Autosomal Recessive 2
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3
    • MENTAL RETARDATION, JOINT HYPERMOBILITY, AND SKIN LAXITY, WITH OR WITHOUT METABOLIC ABNORMALITIES
    • MENTAL RETARDATION, STEREOTYPIC MOVEMENTS, EPILEPSY, AND/OR CEREBRAL MALFORMATIONS
    • Mental Retardation, X-Linked
    • Mental Retardation, X-Linked 1
    • MENTAL RETARDATION, X-LINKED 21
    • Mental Retardation, X-Linked 46
    • Mental Retardation, X-Linked 9
    • Mental retardation, X-linked, syndromic 5
    • Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance
    • Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related
    • Mental Retardation, X-Linked, With Panhypopituitarism
    • Mercury Poisoning
    • Mercury Poisoning, Nervous System
    • Mesothelioma
    • Metabolic Diseases
    • Metabolic Syndrome X
    • Metabolism, Inborn Errors
    • METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY
    • Metal Metabolism, Inborn Errors
    • Metaphyseal chondrodysplasia Schmid type
    • Metaplasia
    • Methemoglobinemia
    • METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE
    • METHIONINE ADENOSYLTRANSFERASE DEFICIENCY
    • Methylmalonic acidemia
    • Methylmalonic acidemia with homocystinuria
    • METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE
    • METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblD TYPE
    • Methylmalonic Aciduria and Homocystinuria, CblF Type
    • Methylmalonic aciduria cblA type
    • Methylmalonic aciduria cblB type
    • Methylmalonyl-CoA Epimerase Deficiency
    • Metrorrhagia
    • Mevalonate Kinase Deficiency
    • Microcephalic osteodysplastic primordial dwarfism, type 2
    • Microcephalic Osteodysplastic Primordial Dwarfism, Type II
    • Microcephaly
    • MICROCEPHALY 1, PRIMARY, AUTOSOMAL RECESSIVE
    • MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE
    • MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE
    • MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE
    • MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE
    • MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE
    • Microcephaly, Primary Autosomal Recessive, 1
    • Microcephaly, Primary Autosomal Recessive, 3
    • Microcephaly, Primary Autosomal Recessive, 4
    • Microcephaly, Primary Autosomal Recessive, 5
    • Microcephaly, Primary Autosomal Recessive, 7
    • Micrognathism
    • Micronuclei, Chromosome-Defective
    • MICROPHTHALMIA, ISOLATED 2
    • Microphthalmia, Isolated 3
    • Microphthalmia, Isolated 4
    • MICROPHTHALMIA, ISOLATED 5
    • Microphthalmia, syndromic 2
    • Microphthalmos
    • Microsatellite Instability
    • MICROTIA, HEARING IMPAIRMENT, AND CLEFT PALATE
    • Microvillus inclusion disease
    • Migraine Disorders
    • Migraine without Aura
    • MIGRAINE, FAMILIAL HEMIPLEGIC, 1
    • Migraine, Familial Hemiplegic, 3
    • Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
    • Mineralocorticoid Excess Syndrome, Apparent
    • Mitochondrial complex I deficiency
    • Mitochondrial Complex II Deficiency
    • MITOCHONDRIAL COMPLEX III DEFICIENCY
    • MITOCHONDRIAL COMPLEX IV DEFICIENCY
    • Mitochondrial Diseases
    • Mitochondrial Encephalomyopathies
    • Mitochondrial encephalopathy
    • Mitochondrial Myopathies
    • Mitochondrial myopathy with lactic acidosis
    • Mitochondrial neurogastrointestinal encephalopathy syndrome
    • Mitochondrial Phosphate Carrier Deficiency
    • Miyoshi Muscular Dystrophy 3
    • Miyoshi myopathy
    • MODY, Type 6
    • Mohr-Tranebjaerg syndrome
    • Molybdenum cofactor deficiency
    • Monilethrix
    • Mononeuropathies
    • Monosomy
    • Mood Disorders
    • MORM syndrome
    • Morphine Dependence
    • Mosaic variegated aneuploidy syndrome
    • Motor Neuron Disease
    • Motor Skills Disorders
    • Mouth Abnormalities
    • Mouth Diseases
    • Mouth Neoplasms
    • Movement Disorders
    • Mowat-Wilson syndrome
    • MUCKLE-WELLS SYNDROME
    • Mucocutaneous Lymph Node Syndrome
    • Mucolipidoses
    • MUCOLIPIDOSIS II ALPHA/BETA
    • MUCOLIPIDOSIS III ALPHA/BETA
    • Mucolipidosis III Gamma
    • MUCOLIPIDOSIS IV
    • Mucopolysaccharidosis I
    • Mucopolysaccharidosis II
    • Mucopolysaccharidosis III
    • Mucopolysaccharidosis IV
    • Mucopolysaccharidosis VI
    • Mucopolysaccharidosis VII
    • Mucositis
    • Muenke Syndrome
    • Muir-Torre Syndrome
    • Mulibrey Nanism
    • Multiple Acyl Coenzyme A Dehydrogenase Deficiency
    • MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY
    • Multiple Chemical Sensitivity
    • Multiple Endocrine Neoplasia
    • Multiple Endocrine Neoplasia Type 1
    • Multiple Endocrine Neoplasia Type 2a
    • Multiple Endocrine Neoplasia Type 2b
    • Multiple Myeloma
    • Multiple Organ Failure
    • Multiple pterygium syndrome
    • MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT
    • MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE
    • Multiple Sclerosis
    • Multiple Sulfatase Deficiency Disease
    • Muscle Hypotonia
    • Muscle Neoplasms
    • Muscle Spasticity
    • Muscle Weakness
    • Muscular Atrophy
    • Muscular Atrophy, Spinal
    • Muscular Diseases
    • Muscular Dystrophies
    • Muscular Dystrophies, Limb-Girdle
    • Muscular dystrophy congenital, merosin negative
    • Muscular Dystrophy, Animal
    • MUSCULAR DYSTROPHY, BECKER TYPE
    • MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A
    • Muscular Dystrophy, Duchenne
    • Muscular Dystrophy, Emery-Dreifuss
    • Muscular Dystrophy, Facioscapulohumeral
    • Muscular Dystrophy, Limb-Girdle, Type 1C
    • MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C
    • MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E
    • MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F
    • Muscular Dystrophy, Limb-Girdle, Type 2G
    • Muscular Dystrophy, Limb-Girdle, Type 2L
    • Muscular Dystrophy, Oculopharyngeal
    • MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1
    • MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2
    • MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4
    • Musculoskeletal Abnormalities
    • Musculoskeletal Diseases
    • Myasthenia Gravis
    • MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
    • Myasthenic Syndrome, Congenital, Fast-Channel
    • Myasthenic syndrome, congenital, postsynaptic slow-channel
    • Myasthenic Syndromes, Congenital
    • Mycobacterium Infections
    • Mycobacterium Infections, Nontuberculous
    • MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO
    • Mycoses
    • Mycosis Fungoides
    • MYD88 Deficiency
    • Mydriasis
    • Myelitis
    • Myelodysplastic Syndromes
    • Myeloproliferative Disorders
    • Myeloproliferative Syndrome, Transient
    • MYH9-Related Disorders
    • Myocardial Infarction
    • Myocardial Ischemia
    • Myocardial Reperfusion Injury
    • Myocarditis
    • Myoclonic dystonia
    • Myoclonic Epilepsies, Progressive
    • MYOCLONIC EPILEPSY, FAMILIAL INFANTILE
    • Myoclonic Epilepsy, Juvenile
    • Myoclonus
    • Myoglobinuria
    • Myopathies, Nemaline
    • Myopathies, Structural, Congenital
    • Myopathy with lactic acidosis and sideroblastic anemia
    • MYOPATHY WITH LACTIC ACIDOSIS, HEREDITARY
    • Myopathy, Central Core
    • MYOPATHY, CENTRONUCLEAR, 1
    • MYOPATHY, CENTRONUCLEAR, 2
    • MYOPATHY, CENTRONUCLEAR, X-LINKED
    • Myopathy, Congenital, Compton-North
    • MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION
    • Myopathy, Distal, with Anterior Tibial Onset
    • MYOPATHY, MYOFIBRILLAR, 3
    • MYOPATHY, MYOFIBRILLAR, 4
    • MYOPATHY, MYOFIBRILLAR, 6
    • MYOPATHY, SPHEROID BODY
    • Myopathy, X-Linked, with Excessive Autophagy
    • MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY
    • Myophosphorylase deficiency
    • Myopia
    • Myositis
    • Myositis Ossificans
    • Myositis, Inclusion Body
    • Myotilinopathy
    • Myotonia
    • Myotonia Congenita
    • MYOTONIA CONGENITA, AUTOSOMAL DOMINANT
    • MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE
    • Myotonic Dystrophy
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