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Azo-Carob Galactomannan

Supplier: Adipogen
Description: Remazol brilliant blue-dyed galactomannan polysaccharide. Soluble substrate for the specific measurement of endo-1,4-beta-D-mannanase/galactomannase. Used for the measurement of enzyme activity, for research, biochemical enzyme assays and in vitro diagnostic analysis.

Product Image-77527-290

Human GM (aspergillus galactomannan) ELISA Kit

Catalog Number: (77527-290)
Supplier: AFG BIOSCIENCE LLC
Description: Human GM (aspergillus galactomannan) ELISA Kit

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Product Image-76578-912

Human Galactomannan (GM) ELISA Kit, AFG Bioscience

Catalog Number: (76578-912)
Supplier: AFG BIOSCIENCE LLC
Description: Human Galactomannan (GM) ELISA Kit, AFG Bioscience
Image Unavailable-10465-372

Anti-GLA Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10465-372)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Image Unavailable-10465-382

Anti-GLA Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10465-382)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Image Unavailable-10815-718

D-Galacto-D-mannan

Supplier: Thermo Scientific Chemicals
Description: D-Galacto-D-Mannan, CAS Number: 11078-30-1, Form: Powder, Color: White, Synonym: Carob galactomannan, Size: 500mg

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Image Unavailable-76119-482

Anti-Galactosidase alpha Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76119-482)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Image Unavailable-89360-338

Anti-GLA Chicken Polyclonal Antibody

Catalog Number: (89360-338)
Supplier: Genetex
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Image Unavailable-10465-376

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

Catalog Number: (10465-376)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Product Image-10465-360

Anti-GLA Rabbit Polyclonal Antibody

Catalog Number: (10465-360)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Image Unavailable-10465-374

Anti-GLA Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10465-374)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Image Unavailable-10465-380

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

Catalog Number: (10465-380)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Image Unavailable-76119-480

Anti-Galactosidase alpha Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76119-480)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Image Unavailable-10465-378

Anti-GLA Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10465-378)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
Image Unavailable-220099-997

AZO-GALACTOMANNAN FROM CAROB

Catalog Number: (220099-997)
Supplier: Sigma Aldrich
Description: AZO-GALACTOMANNAN FROM CAROB

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Image Unavailable-220099-998

AZO-GALACTOMANNAN FROM CAROB

Catalog Number: (220099-998)
Supplier: Sigma Aldrich
Description: AZO-GALACTOMANNAN FROM CAROB

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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.
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