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Product Image-89234-589

Globally Harmonized System (GHS) Centers, Brady®

Catalog Number: (89234-589)
Supplier: Brady Worldwide
Description: These ‘Right To Know Compliance Center’ provides a centralized location for important safety information and makes the information accessible to employees.
Product Image-14214-370

Eyesaver® Deck-Mount Swing-Out Eyewash, Speakman®

Catalog Number: (14214-370)
Supplier: Speakman
Description: Low-profile counter-top eyewash unit for installations where space is at a premium.

Small Business Enterprise


Image Unavailable-102830-018

Human Unprocessed Cord Blood, Charles River Laboratories Cell Solutions

Supplier: Charles River Laboratories Cell Solutions
Description: Human unprocessed cord blood is collected aseptically at the time of delivery from healthy pregnant women

Image Unavailable-10364-012

Anti-RSV Nucleoprotein Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10364-012)
Supplier: Bioss
Description: Respiratory syncytial virus (RSV) is a major cause of respiratory illness in young children. RSV infection produces a variety of signs and symptoms involving different areas of the respiratory tract, from the nose to the lungs. RSV is a negative sense, enveloped RNA virus. The virion is variable in shape and size with average diameter of between 120 and 300 nm.
Product Image-56620-448

PIG® Spill Kit in Large Wall-Mount Cabinet, New Pig

Catalog Number: (56620-448)
Supplier: New Pig
Description: Safety-yellow, heavy-gauge, welded steel cabinet is printed "Spill Kit" for quick identification
Image Unavailable-10451-652

Anti-GORAB Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10451-652)
Supplier: Bioss
Description: Defects in GORAB are the cause of geroderma osteodysplasticum (GO) [MIM:231070]; also known as gerodermia osteodysplastica or Walt Disney dwarfism. GO is a rare autosomal recessive disorder characterized by lax, wrinkled skin, joint laxity and a typical face with a prematurely aged appearance. Skeletal signs include severe osteoporosis leading to frequent fractures, malar and mandibular hypoplasia and a variable degree of growth retardation.
Image Unavailable-101222-914

Human Unprocessed Bone Marrow, Charles River Laboratories Cell Solutions

Supplier: Charles River Laboratories Cell Solutions
Description: Human unprocessed bone marrow is collected via our qualified hospital and physician network from healthy human volunteer donors

Product Image-56620-488

PIG® HazMat Spill Kit in Large Wall-Mount Cabinet, New Pig

Catalog Number: (56620-488)
Supplier: New Pig
Description: Safety-yellow, heavy-gauge, welded steel cabinet is printed "Spill Kit" for quick identification
Image Unavailable-10474-030

Anti-ATXN2 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10474-030)
Supplier: Bioss
Description: The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
Image Unavailable-10474-038

Anti-ATXN2 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10474-038)
Supplier: Bioss
Description: The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
Product Image-10813-992

Anti-IKBKG Rabbit Polyclonal Antibody

Catalog Number: (10813-992)
Supplier: Prosci
Description: Familial incontinentia pigmenti (IP) is a genodermatosis that segregates as an X-linked dominant disorder and is usually lethal prenatally in males. In affected females it causes highly variable abnormalities of the skin, hair, nails, teeth, eyes, and central nervous system. The prominent skin signs occur in 4 classic cutaneous stages: perinatal inflammatory vesicles, verrucous patches, a distinctive pattern of hyperpigmentation, and dermal scarring. Cells expressing the mutated X chromosome are eliminated selectively around the time of birth, so females with IP exhibit extremely skewed X-inactivation.
Image Unavailable-89363-444

Anti-Respiratory Syncytial Virus Mouse Monoclonal Antibody [clone: B023]

Catalog Number: (89363-444)
Supplier: Genetex
Description: Respiratory syncytial virus (RSV) is a major cause of respiratory illness in young children. RSV infection produces a variety of signs and symptoms involving different areas of the respiratory tract, from the nose to the lungs. RSV is a negative sense, enveloped RNA virus. The virion is variable in shape and size with average diameter of between 120 and 300 nm. The 63 kD RSV fusion protein of the RSS 2 strain (subtype A) directs fusion of viral and cellular membranes, results in viral penetration, and can direct fusion of infected cells with adjoining cells, resulting in the formation of syncytia or multi nucleated giant cells.
Image Unavailable-10474-032

Anti-ATXN2 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10474-032)
Supplier: Bioss
Description: The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
Image Unavailable-10451-656

Anti-GORAB Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10451-656)
Supplier: Bioss
Description: Defects in GORAB are the cause of geroderma osteodysplasticum (GO) [MIM:231070]; also known as gerodermia osteodysplastica or Walt Disney dwarfism. GO is a rare autosomal recessive disorder characterized by lax, wrinkled skin, joint laxity and a typical face with a prematurely aged appearance. Skeletal signs include severe osteoporosis leading to frequent fractures, malar and mandibular hypoplasia and a variable degree of growth retardation.
Image Unavailable-76967-434

Anti-Prohibitin Mouse Monoclonal Antibody [clone: PHB/3225]

Catalog Number: (76967-434)
Supplier: ANTIBODIES.COM LLC
Description: Mouse monoclonal [PHB/3225] antibody to Prohibitin for WB, IF and IHC-P with samples derived from Human.
Image Unavailable-76116-946

Anti-ATX2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76116-946)
Supplier: Bioss
Description: The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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