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 • Factor V Heavy Chain (F5) Antibody
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 • Antibiotic resistance marker blaKPC PCR Kit
 • PTPN7 Antibody
 • Haptoglobin precursor (Pre-Hpt) ELISA Kit
 • Thrombin-antithrombin complex (TAT) ELISA Kit
 • MYH15 Antibody
 • Progesterone (PG) Small Molecule
 • EOMES Antibody
 • Aldehyde Dehydrogenase 3 Family, Member A1 (ALDH3A1) ELISA Kit
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 • FBLN5 Antibody
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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    
 C
    • C SYNDROME
    • C-LIKE SYNDROME
    • Cachexia
    • CADASIL
    • Cadmium Poisoning
    • Cafe-au-Lait Spots
    • Calcinosis
    • Calcium Metabolism Disorders
    • Caliciviridae Infections
    • Campomelic Dysplasia
    • Canavan Disease
    • Candidiasis
    • Candidiasis, Familial, 2
    • Candidiasis, Oral
    • Cantu syndrome
    • Capillary Malformation-Arteriovenous Malformation
    • Carbamoyl-Phosphate Synthase I Deficiency Disease
    • Carbohydrate Metabolism, Inborn Errors
    • Carbon Tetrachloride Poisoning
    • CARBOXYPEPTIDASE N DEFICIENCY
    • Carcinogenesis
    • Carcinoid Tumor
    • Carcinoma
    • Carcinoma in Situ
    • Carcinoma, Adenoid Cystic
    • Carcinoma, Basal Cell
    • Carcinoma, Bronchogenic
    • Carcinoma, Ductal, Breast
    • Carcinoma, Embryonal
    • Carcinoma, Endometrioid
    • Carcinoma, Hepatocellular
    • Carcinoma, Large Cell
    • Carcinoma, Lobular
    • Carcinoma, Medullary
    • Carcinoma, Non-Small-Cell Lung
    • Carcinoma, Pancreatic Ductal
    • Carcinoma, Papillary
    • Carcinoma, Renal Cell
    • Carcinoma, Small Cell
    • Carcinoma, Squamous Cell
    • Carcinoma, squamous cell of head and neck
    • Carcinoma, Transitional Cell
    • CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED
    • Cardiac Complexes, Premature
    • Cardiac Output, High
    • Cardiac Output, Low
    • Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
    • Cardiofaciocutaneous syndrome
    • Cardiomegaly
    • Cardiomyopathies
    • Cardiomyopathy, Dilated
    • Cardiomyopathy, Dilated, 1AA
    • Cardiomyopathy, Dilated, 1C
    • CARDIOMYOPATHY, DILATED, 3B
    • Cardiomyopathy, Familial Hypertrophic, 1
    • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
    • Cardiomyopathy, Familial Hypertrophic, 11
    • Cardiomyopathy, Familial Hypertrophic, 13
    • Cardiomyopathy, Familial Hypertrophic, 2
    • Cardiomyopathy, Familial Hypertrophic, 3
    • Cardiomyopathy, Familial Hypertrophic, 4
    • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6
    • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
    • Cardiomyopathy, Familial Hypertrophic, 8
    • Cardiomyopathy, Familial Restrictive, 1
    • Cardiomyopathy, Hypertrophic
    • Cardiomyopathy, Hypertrophic, Familial
    • Cardiomyopathy, Restrictive
    • Cardiovascular Abnormalities
    • Cardiovascular Diseases
    • Carnevale syndrome
    • Carney Complex
    • Carney Complex Variant
    • Carney-Stratakis Syndrome
    • CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
    • CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
    • Carnitine-Acylcarnitine Translocase Deficiency
    • Carotid Artery Diseases
    • Carotid Artery Thrombosis
    • CARPENTER SYNDROME
    • Cartilage Diseases
    • Catalepsy
    • Cataract
    • CATARACT 23
    • Cataract microcornea syndrome
    • CATARACT, AUTOSOMAL DOMINANT
    • CATARACT, CONGENITAL OR JUVENILE
    • CATARACT, CONGENITAL ZONULAR, WITH SUTURAL OPACITIES
    • CATARACT, CONGENITAL, CERULEAN TYPE, 2
    • CATARACT, COPPOCK-LIKE
    • CATARACT, JUVENILE, WITH MICROCORNEA AND GLUCOSURIA
    • CATARACT, LAMELLAR
    • CATARACT, LAMELLAR 2
    • CATARACT, NUCLEAR PROGRESSIVE
    • Cataract, posterior polar, 3
    • Cataract, posterior polar, 4
    • Cataract, zonular
    • CATARACT, ZONULAR PULVERULENT 1
    • CATARACT, ZONULAR PULVERULENT 3
    • Cattle Diseases
    • Caudal regression syndrome
    • CD59 DEFICIENCY
    • Celiac Disease
    • Cell Transformation, Neoplastic
    • Central Nervous System Diseases
    • Central Nervous System Infections
    • Central Nervous System Neoplasms
    • Cerebellar Ataxia
    • Cerebellar Ataxia, Cayman Type
    • Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3
    • Cerebellar Diseases
    • CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY
    • Cerebral Cavernous Malformations 2
    • Cerebral Cavernous Malformations 3
    • Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
    • Cerebral Hemorrhage
    • Cerebral Infarction
    • Cerebral Palsy
    • CEREBROOCULOFACIOSKELETAL SYNDROME 1
    • Cerebrovascular Disorders
    • Ceroid lipofuscinosis, neuronal 1, infantile
    • Ceroid lipofuscinosis, neuronal 3, Juvenile
    • Ceroid lipofuscinosis, neuronal 5
    • Ceroid lipofuscinosis, neuronal 8
    • Ceroid Lipofuscinosis, Neuronal, 1
    • CEROID LIPOFUSCINOSIS, NEURONAL, 2
    • Ceroid Lipofuscinosis, Neuronal, 6
    • CEROID LIPOFUSCINOSIS, NEURONAL, 7
    • Cerulean cataract
    • Cervical Dystonia, Primary
    • Cervical Intraepithelial Neoplasia
    • CHANARIN-DORFMAN SYNDROME
    • Char syndrome
    • Charcot-Marie-Tooth Disease
    • CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE
    • CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B
    • Charcot-Marie-Tooth Disease, Dominant Intermediate C
    • Charcot-Marie-Tooth Disease, Recessive Intermediate A
    • Charcot-Marie-Tooth disease, Type 1B
    • Charcot-Marie-Tooth disease, Type 1C
    • Charcot-Marie-Tooth disease, Type 1F
    • Charcot-Marie-Tooth disease, Type 2B
    • Charcot-Marie-Tooth disease, Type 2B2
    • Charcot-Marie-Tooth disease, Type 2E
    • Charcot-Marie-Tooth disease, Type 2J
    • Charcot-Marie-Tooth disease, Type 2K
    • Charcot-Marie-Tooth disease, Type 4A
    • Charcot-Marie-Tooth disease, Type 4B1
    • Charcot-Marie-Tooth disease, Type 4B2
    • Charcot-Marie-Tooth disease, Type 4C
    • Charcot-Marie-Tooth disease, Type 4E
    • CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
    • Charcot-Marie-Tooth Disease, Type 4j
    • Charcot-Marie-Tooth disease, X-linked, 1
    • CHARGE Syndrome
    • Chediak-Higashi Syndrome
    • Cherubism
    • Chest Pain
    • Chilblain lupus
    • Child Behavior Disorders
    • Child Development Disorders, Pervasive
    • CHOANAL ATRESIA AND LYMPHEDEMA
    • Cholangiocarcinoma
    • Cholangitis
    • Cholangitis, Sclerosing
    • Cholecystitis
    • Cholelithiasis
    • Cholestasis
    • Cholestasis, benign recurrent intrahepatic 1
    • Cholestasis, benign recurrent intrahepatic 2
    • Cholestasis, Intrahepatic
    • Cholestasis, progressive familial intrahepatic 1
    • Cholesterol Ester Storage Disease
    • Chondroblastoma
    • Chondrocalcinosis
    • Chondrodysplasia Punctata
    • Chondrodysplasia punctata, brachytelephalangic
    • Chondrodysplasia Punctata, Rhizomelic
    • Chondrosarcoma
    • CHONDROSARCOMA, EXTRASKELETAL MYXOID
    • Chorea
    • CHOREA, BENIGN HEREDITARY
    • Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress
    • Chorioamnionitis
    • Choriocarcinoma
    • Choroid Diseases
    • Choroidal dystrophy central areolar
    • Choroidal Dystrophy, Central Areolar 2
    • Choroidal Neovascularization
    • Choroideremia
    • Chromosomal Instability
    • Chromosome 17 deletion
    • Chromosome 2q37 deletion syndrome
    • Chromosome 3, monosomy 3p25
    • Chromosome Aberrations
    • Chromosome Breakage
    • Chromosome Xp11.3 Deletion Syndrome
    • Chronic Disease
    • Chronic Pain
    • Chudley-Mccullough syndrome
    • Churg-Strauss Syndrome
    • Chylomicron retention disease
    • CILIARY DYSKINESIA, PRIMARY, 1
    • CILIARY DYSKINESIA, PRIMARY, 11
    • Ciliary Dyskinesia, Primary, 6
    • Ciliary Dyskinesia, Primary, 7
    • CILIARY DYSKINESIA, PRIMARY, 9
    • Ciliary Motility Disorders
    • Citrullinemia
    • CK SYNDROME
    • Classical Lissencephalies and Subcortical Band Heterotopias
    • Cleft Lip
    • Cleft Palate
    • Cleft palate X-linked
    • CLEFT PALATE, ISOLATED
    • Cleft Palate, Isolated, And Mental Retardation
    • Cleidocranial Dysplasia
    • Clubfoot
    • COACH syndrome
    • Cocaine-Related Disorders
    • Cochlear Diseases
    • Cockayne Syndrome
    • COENZYME Q10 DEFICIENCY
    • COENZYME Q10 DEFICIENCY, PRIMARY, 1
    • COENZYME Q10 DEFICIENCY, PRIMARY, 4
    • Coffin-Lowry Syndrome
    • Coffin-Siris syndrome
    • Cognition Disorders
    • Cohen syndrome
    • Cold-Induced Sweating Syndrome 1
    • Colitis
    • Colitis, Ulcerative
    • Coloboma
    • Colonic Diseases
    • Colonic Neoplasms
    • Color Vision Defects
    • COLORECTAL ADENOMATOUS POLYPOSIS, AUTOSOMAL RECESSIVE
    • Colorectal Neoplasms
    • Colorectal Neoplasms, Hereditary Nonpolyposis
    • Coma
    • COMBINED IMMUNODEFICIENCY, X-LINKED
    • Combined Oxidative Phosphorylation Deficiency 1
    • Combined Oxidative Phosphorylation Deficiency 5
    • COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7
    • Common Cold
    • Common Variable Immunodeficiency
    • Community-Acquired Infections
    • COMPLEMENT COMPONENT 2 DEFICIENCY
    • Complement component 5 deficiency
    • COMPLEMENT COMPONENT 6 DEFICIENCY
    • COMPLEMENT COMPONENT 7 DEFICIENCY
    • COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I
    • COMPLEMENT COMPONENT C1r/C1s DEFICIENCY
    • COMPLEMENT FACTOR H DEFICIENCY
    • Conduct Disorder
    • CONE DYSTROPHY 3
    • Cone Dystrophy 4
    • Cone-Rod Dystrophy 13
    • CONE-ROD DYSTROPHY 2
    • Cone-Rod Dystrophy 3
    • CONE-ROD DYSTROPHY 5
    • CONE-ROD DYSTROPHY 6
    • CONE-ROD DYSTROPHY, X-LINKED, 1
    • CONE-ROD DYSTROPHY, X-LINKED, 3
    • Confusion
    • Congenital Abnormalities
    • Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency
    • Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
    • Congenital Cataracts, Facial Dysmorphism, And Neuropathy
    • Congenital central hypoventilation syndrome
    • Congenital contractural arachnodactyly
    • Congenital diaphragmatic hernia
    • Congenital disorder of glycosylation type 1A
    • Congenital disorder of glycosylation type 1D
    • Congenital disorder of glycosylation type 1J
    • Congenital disorder of glycosylation type 1L
    • Congenital disorder of glycosylation, type 2C
    • Congenital Disorder Of Glycosylation, Type IIB
    • CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc
    • Congenital Disorder Of Glycosylation, Type IIF
    • Congenital Disorder Of Glycosylation, Type IIH
    • CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi
    • CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj
    • CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip
    • Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects
    • Congenital Hyperinsulinism
    • Congenital Hypothyroidism
    • Congenital, Hereditary, and Neonatal Diseases and Abnormalities
    • Conjunctival Diseases
    • Conjunctivitis
    • Conjunctivitis, Allergic
    • Connective Tissue Diseases
    • Conotruncal cardiac defects
    • CONOTRUNCAL HEART MALFORMATIONS
    • Consciousness Disorders
    • Constipation
    • Contracture
    • Coproporphyria, Hereditary
    • Cornea Plana 2
    • Corneal Diseases
    • Corneal Dystrophies, Hereditary
    • Corneal dystrophy and perceptive deafness
    • Corneal dystrophy Avellino type
    • Corneal dystrophy crystalline of Schnyder
    • Corneal Dystrophy, Crystalline, of Schnyder
    • CORNEAL DYSTROPHY, FLECK
    • Corneal Dystrophy, Fuchs Endothelial, 4
    • Corneal dystrophy, gelatinous drop-like
    • Corneal Dystrophy, Juvenile Epithelial of Meesmann
    • Corneal Dystrophy, Lattice Type IIIA
    • Corneal Dystrophy, Posterior Polymorphous, 1
    • Corneal Dystrophy, Posterior Polymorphous, 2
    • Corneal endothelial dystrophy type 2
    • Coronary Aneurysm
    • Coronary Artery Disease
    • Coronary Disease
    • Coronary Restenosis
    • Coronary Thrombosis
    • Coronary Vasospasm
    • Coronavirus Infections
    • Corpus callosum agenesis neuronopathy
    • CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA
    • Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia
    • CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY
    • Cortisone reductase deficiency
    • Costeff optic atrophy syndrome
    • Costello Syndrome
    • Cough
    • Coumarin Resistance
    • COUSIN SYNDROME
    • Coxsackievirus Infections
    • Craniocerebral Trauma
    • Cranioectodermal Dysplasia
    • CRANIOECTODERMAL DYSPLASIA 2
    • Craniofacial Abnormalities
    • Craniofacial Dysostosis
    • Craniofrontonasal dysplasia
    • CRANIOFRONTONASAL SYNDROME
    • CRANIOLENTICULOSUTURAL DYSPLASIA
    • Craniometaphyseal Dysplasia, Autosomal Dominant
    • Craniosynostoses
    • Craniosynostosis radial aplasia syndrome
    • CRANIOSYNOSTOSIS, TYPE 1
    • CRANIOSYNOSTOSIS, TYPE 2
    • Creatine deficiency, X-linked
    • Creutzfeldt-Jakob Syndrome
    • Cri-du-Chat Syndrome
    • Crigler Najjar syndrome, type 1
    • Crigler-Najjar Syndrome
    • Crisponi syndrome
    • Crohn Disease
    • Crouzon Syndrome With Acanthosis Nigricans
    • Cryopyrin-Associated Periodic Syndromes
    • Cryptococcosis
    • Cryptorchidism
    • CRYPTORCHIDISM, UNILATERAL OR BILATERAL
    • Currarino triad
    • Cushing Syndrome
    • Cutis Laxa
    • CUTIS LAXA, AUTOSOMAL DOMINANT
    • CUTIS LAXA, AUTOSOMAL DOMINANT 1
    • CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE I
    • Cutis Laxa, Autosomal Recessive, Type IIA
    • Cutis Laxa, Autosomal Recessive, Type IIB
    • Cyanosis
    • Cyclic neutropenia
    • Cystadenoma
    • Cystic Fibrosis
    • CYSTIC FIBROSIS, MODIFIER OF, 1
    • Cystinosis
    • CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE
    • Cystinosis, ocular nonnephropathic
    • Cystinuria
    • Cystitis
    • Cysts
    • Cytochrome-c Oxidase Deficiency
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Diseases Name 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    
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