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Product Image-ACRO103925000

5-Aminolevulinic acid hydrochloride 98+%

Fournisseur: Thermo Fisher Scientific
Description: CAS No.: 5451-09-2

FDS (Fiche de données de sécurité)

Image Unavailable-APOSOR1490-25G

5-Aminolevulinic acid hydrochloride 97%

Fournisseur: Apollo Scientific
Description: 5-Aminolevulinic acid hydrochloride 97%

Image Unavailable-A16942.MC

5-Aminolevulinic acid hydrochloride 99%

Fournisseur: Thermo Fisher Scientific
Description: 5-Aminolevulinic acid hydrochloride 99%

FDS (Fiche de données de sécurité) Certificats.

Image Unavailable-1025737.

Aminolevulinic Acid, Reference Standards

Fournisseur: USP
Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

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5-Aminolevulinic acid hydrochloride ≥98%, en poudre

Fournisseur: MP Biomedicals
Description: δ-Aminolevulinic acid hydrochloride is the universal precursor of tetrapyrroles, such as chlorophyll and heme.
δ-Aminolevulinic acid hydrochloride is used in the synthesis of hemes, vitamin B12 and bacteriochlorophyll. It is used in porphyrin biosynthesis studies. It enhances chlorophyll formation and may be used as a photodynamic herbicide is a precursor of tetrapyrroles in the biosynthesis of chlorophyll and heme.
5-Aminolevulinic acid (5-ALA) is an intermediate in heme biosynthesis and is being studied as an inducing reagent for protoporphyrin IX (PPIX) dependent fluorescence diagnosis of metastatic lymph nodes. 5-ALA is used for photodynamic therapy of diseases such as Paget’s disease and HPV infection-associated cervical condylomata acuminata.

Image Unavailable-BOSSBS-9068R

Anti-HMBS Rabbit Polyclonal Antibody

Référence Produit: (BOSSBS-9068R)
Fournisseur: 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
Image Unavailable-BOSSBS-9068R-HRP

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

Référence Produit: (BOSSBS-9068R-HRP)
Fournisseur: 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
Image Unavailable-BOSSBS-9068R-A488

Anti-HMBS Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Référence Produit: (BOSSBS-9068R-A488)
Fournisseur: 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
Image Unavailable-BOSSBS-9068R-CY5.5

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

Référence Produit: (BOSSBS-9068R-CY5.5)
Fournisseur: 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
Image Unavailable-BOSSBS-9068R-CY7

Anti-HMBS Rabbit Polyclonal Antibody (Cy7®)

Référence Produit: (BOSSBS-9068R-CY7)
Fournisseur: 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
Image Unavailable-BOSSBS-9068R-A680

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

Référence Produit: (BOSSBS-9068R-A680)
Fournisseur: 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 characterised 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
Image Unavailable-BOSSBS-9068R-A647

Anti-HMBS Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Référence Produit: (BOSSBS-9068R-A647)
Fournisseur: 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
Image Unavailable-BOSSBS-9068R-CY5

Anti-HMBS Rabbit Polyclonal Antibody (Cy5®)

Référence Produit: (BOSSBS-9068R-CY5)
Fournisseur: 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
Image Unavailable-BOSSBS-9068R-FITC

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

Référence Produit: (BOSSBS-9068R-FITC)
Fournisseur: 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
Image Unavailable-BOSSBS-9068R-A750

Anti-HMBS Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Référence Produit: (BOSSBS-9068R-A750)
Fournisseur: 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 characterised 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
Image Unavailable-BOSSBS-9068R-CY3

Anti-HMBS Rabbit Polyclonal Antibody (Cy3®)

Référence Produit: (BOSSBS-9068R-CY3)
Fournisseur: 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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