Print…

You Searched For: Homogentisic+acid


165,819  results were found

Refine Results Sort by
SearchResultCount:"165819"

Sort Results

List View Easy View

Rate These Search Results

Image Unavailable-100264-938

Homogentisic acid ≥95% (by HPLC)

Catalog Number: (100264-938)
Supplier: Indofine Chemical Company
Description: Rare Organics & BioChemicals 451-13-8 1gm 2,5-Dihydroxyphenylacetic acid 168.15 Room temperature.

Small Business Enterprise Minority or Woman-Owned Business Enterprise


Image Unavailable-10319-480

Anti-HGD Rabbit Polyclonal Antibody (FITC)

Catalog Number: (10319-480)
Supplier: Bioss
Description: 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.
Image Unavailable-77237-004

Homogentisic acid-γ-lactone 98%

Supplier: Ambeed
Description: 5-Hydroxybenzofuran-2(3H)-one, Purity: 98%, CAS Number: 2688-48-4, Appearance: Form: powder Colour: light yellow - dark brown, Storage: Sealed in dry, Room Temperature, Size: 5g

Image Unavailable-TCD1050-005G

Homogentisic acid ≥97.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 451-13-8
MDL Number: MFCD00004324
Molecular Formula: C8H8O4
Molecular Weight: 168.15
Purity/Analysis Method: >97.0% (HPLC,T)
Form: Crystal
Melting point (°C): 147

SDS Certificates

Image Unavailable-10319-482

Anti-HGD Rabbit Polyclonal Antibody (HRP)

Catalog Number: (10319-482)
Supplier: Bioss
Description: 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.
Image Unavailable-TCH0630-005G

Homogentisic acid-γ-lactone ≥98.0%

Supplier: TCI America
Description: CAS Number: 2688-48-4
MDL Number: MFCD00005857
Molecular Formula: C8H6O3
Molecular Weight: 150.13
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 193

SDS

Image Unavailable-76099-998

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

Catalog Number: (76099-998)
Supplier: Bioss
Description: 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.
Image Unavailable-10319-478

Anti-HGD Rabbit Polyclonal Antibody (Cy7)

Catalog Number: (10319-478)
Supplier: Bioss
Description: 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.
Image Unavailable-102990-216

4-Hydroxyphenylpyruvic Acid

Supplier: Adipogen
Description: Keto acid that is involved in the tyrosine catabolism pathway. It is a product of the enzyme (R)-4-hydroxyphenyllactate dehydrogenase and is formed during tyrosine metabolism. The conversion from tyrosine to 4-HPPA is catalyzed by tyrosine aminotransferase. 4-HPPA can be converted to homogentisic acid which is one of the precursors to ochronotic pigment. A deficiency in the catalytic activity of HPD is known to lead to tyrosinemia type III, an autosomal recessive disorder characterized by elevated levels of blood tyrosine and massive excretion of tyrosine derivatives into urine.

Image Unavailable-75790-626

Human Recombinant 4HPPD (from E. coli)

Catalog Number: (75790-626)
Supplier: Prosci
Description: 4-Hydroxyphenylpyruvate Dioxygenase (4HPPD) belongs to the 4HPPD family. 4HPPD is a key enzyme in the degradation of tyrosine, which catalyzes the second reaction in the catabolism of tyrosine the conversation of 4-hydroxyphenylpyruvate to homogentisate. 4HPPD exists in homodimer forms, which uses zinc as a cofactor to catalyze the third step in the conversion of L-phenylalanine to fumarate and acetoacetic acid. When the active 4HPPD enzyme concentration is low in the human body, it results in high levels of tyrosine concentration in the blood, which can cause mild mental retardation at birth, and degradation in vision as a patient grows older.
Image Unavailable-103283-004

Anti-HGD Rabbit Polyclonal Antibody

Catalog Number: (103283-004)
Supplier: Novus Biologicals
Description: The HGD Antibody from Novus Biologicals is a rabbit polyclonal antibody to HGD. This antibody reacts with human. The HGD Antibody has been validated for the following applications: Western Blot, Immunohistochemistry, Immunocytochemistry / Immunofluorescence, Immunohistochemistry-Paraffin.
Image Unavailable-103458-688

Anti-HPD Rabbit Polyclonal Antibody

Catalog Number: (103458-688)
Supplier: Affymetrix, Inc.
Description: This Antibody targets HPD in WB applications and shows reactivity with Human samples. The immunogen is recombinant fragment corresponding to a region within amino acids 49 and 323 of Human HPD. The protein encoded by this gene is an enzyme in the catabolic pathway of tyrosine. The encoded protein catalyzes the conversion of 4-hydroxyphenylpyruvate to homogentisate. Defects in this gene are a cause of tyrosinemia type 3 (TYRO3) and hawkinsinuria (HAWK). Two transcript variants encoding different isoforms have been found for this gene.

Blocked
Image Unavailable-76100-000

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

Catalog Number: (76100-000)
Supplier: Bioss
Description: 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.
Image Unavailable-10319-476

Anti-HGD Rabbit Polyclonal Antibody (Cy5)

Catalog Number: (10319-476)
Supplier: Bioss
Description: 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.
Image Unavailable-10319-474

Anti-HGD Rabbit Polyclonal Antibody (Cy3)

Catalog Number: (10319-474)
Supplier: Bioss
Description: 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.
Image Unavailable-89268-136

Anti-HGD Rabbit Polyclonal Antibody

Catalog Number: (89268-136)
Supplier: Genetex
Description: Rabbit polyclonal antibody to HGD (Middle)
Inquire for Price
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.
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.
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 Regulatory_Affairs@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 organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
1 - 16 of 165,819
no targeter for Bottom