Print…

U heeft gezocht op: Zinc(II)+acetylacetonate


32 822  results were found

Verfijn resultaten Sorteren bij
SearchResultCount:"32822"

Sort Results

List view Easy View (new)

Rate These Search Results

Image Unavailable-BOSSBS-8414R-CY7

Anti-HAGHL Rabbit Polyclonal Antibody (Cy7®)

Catalogus nummer: (BOSSBS-8414R-CY7)
Leverancier: Bioss
Omschrijving: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8414R

Anti-HAGHL Rabbit Polyclonal Antibody

Catalogus nummer: (BOSSBS-8414R)
Leverancier: Bioss
Omschrijving: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8414R-A488

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

Catalogus nummer: (BOSSBS-8414R-A488)
Leverancier: Bioss
Omschrijving: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Image Unavailable-14439-1KG

Zinkoxide 99-100.5% (dried basis), Puriss., meets analytical specification of BP, Ph. Eur., USP, Fluka™

Catalogus nummer: (14439-1KG)
Leverancier: Honeywell Chemicals
Omschrijving: Zinkoxide 99-100.5% (dried basis), Puriss., meets analytical specification of BP, Ph. Eur., USP, Fluka™
UOM: 1 * 1 kg

MSDS


Image Unavailable-J62160.AE

Zinkchloride 25 mM in aqueous solution

Catalogus nummer: (J62160.AE)
Leverancier: Thermo Fisher Scientific
Omschrijving: Zinkchloride 25 mM in aqueous solution
UOM: 1 * 100 mL

MSDS Certificaten


Product Image-20081.298

2,4-Pentaandion ≥99%, TECHNICAL

Catalogus nummer: (20081.298)
Leverancier: VWR Chemicals
Omschrijving: 2,4-Pentaandion ≥99%, TECHNICAL
UOM: 1 * 1 L

MSDS Certificaten


Image Unavailable-30529.09

(2,4-Pentanedionato)lithium ≥99.5%

Leverancier: Thermo Fisher Scientific
Omschrijving: (2,4-Pentanedionato)lithium ≥99.5%

MSDS Certificaten

Image Unavailable-J60963.AE

Zinksulfaat 100 mM in aqueous solution

Catalogus nummer: (J60963.AE)
Leverancier: Thermo Fisher Scientific
Omschrijving: Zinksulfaat 100 mM in aqueous solution
UOM: 1 * 100 mL

MSDS Certificaten


Image Unavailable-BOSSBS-8414R-A350

Anti-HAGHL Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalogus nummer: (BOSSBS-8414R-A350)
Leverancier: Bioss
Omschrijving: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8414R-A555

Anti-HAGHL Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalogus nummer: (BOSSBS-8414R-A555)
Leverancier: Bioss
Omschrijving: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8414R-A750

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

Catalogus nummer: (BOSSBS-8414R-A750)
Leverancier: Bioss
Omschrijving: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8414R-FITC

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

Catalogus nummer: (BOSSBS-8414R-FITC)
Leverancier: Bioss
Omschrijving: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8414R-CY5

Anti-HAGHL Rabbit Polyclonal Antibody (Cy5®)

Catalogus nummer: (BOSSBS-8414R-CY5)
Leverancier: Bioss
Omschrijving: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Image Unavailable-B24009.18

Sodium 2,4-pentanedionate hydrate 95%

Leverancier: Thermo Fisher Scientific
Omschrijving: Sodium 2,4-pentanedionate hydrate 95%

MSDS

Image Unavailable-BOSSBS-8414R-A680

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

Catalogus nummer: (BOSSBS-8414R-A680)
Leverancier: Bioss
Omschrijving: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Product Image-20092.230

2,4-Pentaandion ≥99.0%, AnalaR NORMAPUR® analytical reagent

Catalogus nummer: (20092.230)
Leverancier: VWR Chemicals
Omschrijving: 2,4-Pentaandion ≥99.0%, AnalaR NORMAPUR® analytical reagent
UOM: 1 * 250 mL

MSDS Certificaten


Bel voor prijs
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.
Dit artikel is geblokkeerd voor uw organisatie. Neem contact op met uw inkoopafdeling voor meer informatie
Het orginele artikel is niet langer beschikbaar. Het alternatief dat wordt getoond is beschikbaar
Product(en) gemarkeerd met dit symbool worden niet meer verkocht cq verkocht tot het einde van de voorraad. Alternatieven zijn mogelijk beschikbaar door te zoeken met het VWR-catalogusnummer dat hierboven wordt vermeld. Voor meer informatie kunt u contact opnemen met customer service: 020-4808410.
337 - 352 of 32 822
no targeter for Bottom