Hai cercato: Methyl-5-aminolevulinate+hydrochloride

Fornitore: TCI EUROPE

Descrizione: Methyl-5-aminolevulinate hydrochloride ≥98.0% (by total nitrogen and titration analysis)

Fornitore: Apollo Scientific

Descrizione: 5-Aminolevulinic acid hydrochloride 97%

Fornitore: TCI EUROPE

Descrizione: 5-Aminolevulinic acid hydrochloride ≥98.0% (by titrimetric analysis)

Fornitore: Thermo Scientific

Descrizione: CAS No.: 5451-09-2

MSDS

Fornitore: Thermo Scientific

Descrizione: 5-Aminolevulinic acid hydrochloride 99%

MSDS

Fornitore: USP

Descrizione: 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.

Fornitore: MP Biomedicals

Descrizione: 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.

Codice catalogo: (BOSSBS-9068R-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-9068R-A488

Codice articolo locale: BOSSBS-9068R-A488

Descrizione: 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

Promo

Codice catalogo: (BOSSBS-9527R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-9527R-CY5

Codice articolo locale: BOSSBS-9527R-CY5

Descrizione: 5-aminolevulinate synthase 1 (ALAS-H) and 2 (ALAS-E) are two isoforms of ALAS, an enzyme catalyzing the first step of the heme biosynthetic pathway in mammals. The erythroid-specific isoenzyme, ALAS-E, regulates the first step of hematopoietic cell differentation and iron metabolism in the liver. ALAS-H is a housekeeping protein which mediates synthesis of early heme in the mitochondria of most cells. Succinyl CoA associates with ALAS-E in protein conformation change and translocation of ALAS-E into the mitochondria and does not interact with ALAS-H. The ALAS-E 5'-flanking region contains binding sites for nuclear activators such as GATA-1, NF-E2 and EKLF. Since the ALAS gene maps to the X chromosome, mutation of the gene leads to the pyridoxine-refractory X-linked sideroblastic anemia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9527R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-9527R-CY7

Codice articolo locale: BOSSBS-9527R-CY7

Descrizione: 5-aminolevulinate synthase 1 (ALAS-H) and 2 (ALAS-E) are two isoforms of ALAS, an enzyme catalyzing the first step of the heme biosynthetic pathway in mammals. The erythroid-specific isoenzyme, ALAS-E, regulates the first step of hematopoietic cell differentation and iron metabolism in the liver. ALAS-H is a housekeeping protein which mediates synthesis of early heme in the mitochondria of most cells. Succinyl CoA associates with ALAS-E in protein conformation change and translocation of ALAS-E into the mitochondria and does not interact with ALAS-H. The ALAS-E 5'-flanking region contains binding sites for nuclear activators such as GATA-1, NF-E2 and EKLF. Since the ALAS gene maps to the X chromosome, mutation of the gene leads to the pyridoxine-refractory X-linked sideroblastic anemia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9516R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-9516R-CY3

Codice articolo locale: BOSSBS-9516R-CY3

Descrizione: 5-aminolevulinate synthase 1 (ALAS-H) and 2 (ALAS-E) are two isoforms of ALAS, an enzyme catalyzing the first step of the heme biosynthetic pathway in mammals. The erythroid-specific isoenzyme, ALAS-E, regulates the first step of hematopoietic cell differentation and iron metabolism in the liver. ALAS-H is a housekeeping protein which mediates synthesis of early heme in the mitochondria of most cells. Succinyl CoA associates with ALAS-E in protein conformation change and translocation of ALAS-E into the mitochondria and does not interact with ALAS-H. The ALAS-E 5'-flanking region contains binding sites for nuclear activators such as GATA-1, NF-E2 and EKLF. Since the ALAS gene maps to the X chromosome, mutation of the gene leads to the pyridoxine-refractory X-linked sideroblastic anemia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9527R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-9527R-A350

Codice articolo locale: BOSSBS-9527R-A350

Descrizione: 5-aminolevulinate synthase 1 (ALAS-H) and 2 (ALAS-E) are two isoforms of ALAS, an enzyme catalyzing the first step of the heme biosynthetic pathway in mammals. The erythroid-specific isoenzyme, ALAS-E, regulates the first step of hematopoietic cell differentation and iron metabolism in the liver. ALAS-H is a housekeeping protein which mediates synthesis of early heme in the mitochondria of most cells. Succinyl CoA associates with ALAS-E in protein conformation change and translocation of ALAS-E into the mitochondria and does not interact with ALAS-H. The ALAS-E 5'-flanking region contains binding sites for nuclear activators such as GATA-1, NF-E2 and EKLF. Since the ALAS gene maps to the X chromosome, mutation of the gene leads to the pyridoxine-refractory X-linked sideroblastic anemia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9516R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-9516R-A750

Codice articolo locale: BOSSBS-9516R-A750

Descrizione: 5-aminolevulinate synthase 1 (ALAS-H) and 2 (ALAS-E) are two isoforms of ALAS, an enzyme catalyzing the first step of the heme biosynthetic pathway in mammals. The erythroid-specific isoenzyme, ALAS-E, regulates the first step of hematopoietic cell differentiation and iron metabolism in the liver. ALAS-H is a housekeeping protein which mediates synthesis of early heme in the mitochondria of most cells. Succinyl CoA associates with ALAS-E in protein conformation change and translocation of ALAS-E into the mitochondria and does not interact with ALAS-H. The ALAS-E 5'-flanking region contains binding sites for nuclear activators such as GATA-1, NF-E2 and EKLF. Since the ALAS gene maps to the X chromosome, mutation of the gene leads to the pyridoxine-refractory X-linked sideroblastic anemia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (USBI031764-APC)

Fornitore: US Biological

Codice articolo fornitore: 031764-APC

Codice articolo locale: USBI031764-APC

Descrizione: Anti-ALAS2 Rabbit Polyclonal Antibody (APC (Allophycocyanin))

UOM: 1 * 200 µl

Promo

Codice catalogo: (BOSSBS-9068R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-9068R-A750

Codice articolo locale: BOSSBS-9068R-A750

Descrizione: 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

Promo

Codice catalogo: (BOSSBS-9068R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-9068R-CY7

Codice articolo locale: BOSSBS-9068R-CY7

Descrizione: 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

Promo