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Image Unavailable-8.20587.0025

Monoethyl fumarate iron (II,III) salt per sintesi

Codice catalogo: (8.20587.0025)
Fornitore: Merck
Codice articolo fornitore: 8.20587.0025
Codice articolo locale: MERC8.20587.0025
Descrizione: Monoethyl fumarate iron (II,III) salt per sintesi
UOM: 1 * 25 g
Image Unavailable-B23956.0B

Iron(II) fumarate 94%

Fornitore: Thermo Scientific
Descrizione: Iron(II) fumarate 94%

MSDS Certificati

Sistemi per acqua ultrapura Sartorius Arium® Mini

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ULTERIORI INFORMAZIONI

fino a 10 l, tipo 1/al giorno

ACQUISTA ORA
Image Unavailable-SPCMFE108-12KG

Iron(II) fumarate ≥97.0% USP

Fornitore: Spectrum Chemical
Descrizione: Ferrous Fumarate, USP is a mineral supplement.

Image Unavailable-BOSSBS-15472R-HRP

Anti-HGD Rabbit Polyclonal Antibody (HRP)

Codice catalogo: (BOSSBS-15472R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-HRP
Codice articolo locale: BOSSBS-15472R-HRP
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-FITC

Anti-HGD Rabbit Polyclonal Antibody (FITC)

Codice catalogo: (BOSSBS-15472R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-FITC
Codice articolo locale: BOSSBS-15472R-FITC
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R

Anti-HGD Rabbit Polyclonal Antibody

Codice catalogo: (BOSSBS-15472R)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R
Codice articolo locale: BOSSBS-15472R
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyze the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterized by urine that turns dark on standing and alkalinization, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-CY7

Anti-HGD Rabbit Polyclonal Antibody (Cy7)

Codice catalogo: (BOSSBS-15472R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-CY7
Codice articolo locale: BOSSBS-15472R-CY7
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-A488

Anti-HGD Rabbit Polyclonal Antibody (ALEXA FLUOR® 488)

Codice catalogo: (BOSSBS-15472R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-A488
Codice articolo locale: BOSSBS-15472R-A488
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-A647

Anti-HGD Rabbit Polyclonal Antibody (ALEXA FLUOR® 647)

Codice catalogo: (BOSSBS-15472R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-A647
Codice articolo locale: BOSSBS-15472R-A647
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-CY5

Anti-HGD Rabbit Polyclonal Antibody (Cy5)

Codice catalogo: (BOSSBS-15472R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-CY5
Codice articolo locale: BOSSBS-15472R-CY5
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-CY3

Anti-HGD Rabbit Polyclonal Antibody (Cy3)

Codice catalogo: (BOSSBS-15472R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-CY3
Codice articolo locale: BOSSBS-15472R-CY3
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-A555

Anti-HGD Rabbit Polyclonal Antibody (ALEXA FLUOR® 555)

Codice catalogo: (BOSSBS-15472R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-A555
Codice articolo locale: BOSSBS-15472R-A555
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-A680

Anti-HGD Rabbit Polyclonal Antibody (ALEXA FLUOR® 680)

Codice catalogo: (BOSSBS-15472R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-A680
Codice articolo locale: BOSSBS-15472R-A680
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-A350

Anti-HGD Rabbit Polyclonal Antibody (ALEXA FLUOR® 350)

Codice catalogo: (BOSSBS-15472R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-A350
Codice articolo locale: BOSSBS-15472R-A350
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15472R-A750

Anti-HGD Rabbit Polyclonal Antibody (ALEXA FLUOR® 750)

Codice catalogo: (BOSSBS-15472R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-15472R-A750
Codice articolo locale: BOSSBS-15472R-A750
Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl
Image Unavailable-44948-250G

Iron(II) gluconate hydrate, Supelco®

Codice catalogo: (44948-250G)
Fornitore: Merck
Codice articolo fornitore: 44948-250G
Codice articolo locale: SUPL44948-250G
Descrizione: Iron(II) gluconate hydrate, Supelco®
UOM: 1 * 250 g
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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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