You Searched For: Bzl-Gly-OH


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Catalog Number: (APOSOR1013028-500G)
Supplier: Apollo Scientific
Description: Dl-Cysteine Hydrochloride Monohydrate 500g pack 1 * 500 g
UOM: 1 * 500 g

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Catalog Number: (APOSOR926486-500G)
Supplier: Apollo Scientific
Description: Sodium 1-hexane sulfonate monohydrate 500g pack 1 * 500 g
UOM: 1 * 500 g

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Catalog Number: (APOSOR1015009-500G)
Supplier: Apollo Scientific
Description: Sodium Anthraquinone-2-Sulfonate Monohydrate 500g pack 1 * 500 g
UOM: 1 * 500 g

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Catalog Number: (ACRO406380000)
Supplier: Thermo Fisher Scientific
Description: 6,9-Diamino-2-ethoxyacridine lactate monohydrate, 95% 1 * 1 kg
UOM: 1 * 1 kg


Catalog Number: (APOSOR1013033-250G)
Supplier: Apollo Scientific
Description: DL-Glutamic acid monohydrate 250g pack 1 * 250 g
UOM: 1 * 250 g

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Catalog Number: (APOSOR1014945-2.5)
Supplier: Apollo Scientific
Description: Sodium 1-octanesulfonate monohydrate 2.5kg pack 1 * 2,5 kg
UOM: 1 * 2,5 kg

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Catalog Number: (APOSIN10634-500G)
Supplier: Apollo Scientific
Description: Tri-Potassium Phosphate Monohydrate 500g pack 1 * 500 g
UOM: 1 * 500 g

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Catalog Number: (APOSIN1533-50G)
Supplier: Apollo Scientific
Description: Copper(II) acetate monohydrate 50g pack 1 * 50 g
UOM: 1 * 50 g

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Catalog Number: (APOSOR1009488-100G)
Supplier: Apollo Scientific
Description: 1-Hexadecyl-3-Methylimidazolium Chloride Monohydrate 100g pack 1 * 100 g
UOM: 1 * 100 g

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Catalog Number: (APOSOR1013028-100G)
Supplier: Apollo Scientific
Description: Dl-Cysteine Hydrochloride Monohydrate 100g pack 1 * 100 g
UOM: 1 * 100 g

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Catalog Number: (BOSSBS-9068R-CY5.5)
Supplier: Bioss
Description: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-9068R-CY7)
Supplier: Bioss
Description: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-9068R-CY3)
Supplier: Bioss
Description: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
UOM: 1 * 100 µl


Catalog Number: (APOSOR1009488-500G)
Supplier: Apollo Scientific
Description: 1-Hexadecyl-3-Methylimidazolium Chloride Monohydrate 500g pack 1 * 500 g
UOM: 1 * 500 g

New Product


Catalog Number: (APOSOR1010020-25G)
Supplier: Apollo Scientific
Description: 2,4,6-Trihydroxybenzoic Acid Monohydrate 25g pack 1 * 25 g
UOM: 1 * 25 g

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Catalog Number: (BOSSBS-9068R-A647)
Supplier: Bioss
Description: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
UOM: 1 * 100 µl


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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 on +353 1 88 22222.
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 on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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