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2,4-Difluoro-3-(methoxymethyl)benzoic+acid
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2,4-Difluoro-3-(methoxymethyl)benzoic+acid
Catalog Number:
(101916-356)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 058926-1G , MDL Number: MFCD18384846
Supplier:
Bachem Americas
Description:
Please see also α-MSH (corresponds to acetyl-ACTH (1-13) amide, H-1075), α-MSH (free acid) (acetyl-ACTH (1-13), H-1070), and (Des-acetyl)-α-MSH (H-4390). Wied: Pituitary Adrenal System Hormones and Behaviour. Symposium on Developments in Endocrinology (1976) / Anon.: ACTH and Related Peptides: Structure, Regulation, and Action. Ann. N.Y. Acad. Sci. 297, 1 (1977) / A.V.Schally: Aspects of Hypothalamic Regulation of the Pituitary Gland. Science 202, 18 (1978) / R.Schwyzer: Studies on Polypeptide Receptors. A Critical View on the Mechanism of ACTH Action. Bull. Schweiz. Acad. Med. Wiss. 34, 263 (1978).
Catalog Number:
(80050-386)
Supplier:
MilliporeSigma
Description:
Ca2+ chelator exhibiting a 105-fold greater affinity for Ca2+ .
Supplier:
TCI America
Description:
CAS Number: 537-98-4
MDL Number: MFCD00004400 Molecular Formula: C10H10O4 Molecular Weight: 194.19 Purity/Analysis Method: >98.0% (GC,T) Form: Crystal Melting point (°C): 173
Catalog Number:
(89515-082)
Supplier:
Abgent
Description:
polyclonal antibody Isotype: Rabbit Ig, Species Reactivity: human, Gene ID: 3163, Target/specificity: This HMOX2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 24-52 amino acids from the N-terminal region of human HMOX2.
Supplier:
Bachem Americas
Description:
Please see also α-MSH (corresponds to acetyl-ACTH (1-13) amide, H-1075), α-MSH (free acid) (acetyl-ACTH (1-13), H-1070), and (Des-acetyl)-α-MSH (H-4390). For reviews on ACTH and related peptides see: D.de Wied: Pituitary Adrenal System Hormones and Behaviour. Symposium on Developments in Endocrinology (1976) / Anon.: ACTH and Related Peptides: Structure, Regulation, and Action. Ann. N.Y. Acad. Sci. 297, 1 (1977) / A.V.Schally: Aspects of Hypothalamic Regulation of the Pituitary Gland. Science 202, 18 (1978) / R.Schwyzer: Studies on Polypeptide Receptors. A Critical View on the Mechanism of ACTH Action. Bull. Schweiz. Acad. Med. Wiss. 34, 263 (1978).
Catalog Number:
(77436-916)
Supplier:
Bioss
Description:
Osteocalcin belongs to the osteocalcin/matrix Gla protein family and constitutes 1 to 2% of the total bone protein. It is a 49 amino acid single chain vitamin K dependent protein, made by osteoblasts, and is a major component of the noncollagenous bone matrix. Post translational modification by a vitamin K dependent carboxylase produces three gamma carboxyglutamic acid residues at positions 17, 21 and 24, giving it a high affinity for calcium. It also binds strongly to apatite.
Supplier:
TCI America
Description:
CAS Number: 129460-09-9
MDL Number: MFCD00065631 Molecular Formula: C23H25NO6 Molecular Weight: 411.45 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Specific rotation [a]20/D: -24 deg (C=1, DMF)
Catalog Number:
(101935-172)
Supplier:
Matrix Scientific
Description:
MF=C16H21No4 MW=291.35 250Mg
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 056462-1G , MDL Number: MFCD03839866
Supplier:
TCI America
Description:
(stabilized with BHT)
CAS Number: 1025-15-6
MDL Number: MFCD00006554
Molecular Formula: C12H15N3O3
Molecular Weight: 249.27
Purity/Analysis Method: <gt/>96.0% (GC)
Form: Crystal
Boiling point (°C): 140
Flash Point (°C): 245
Freezing point (°C): 24
Supplier:
ALADDIN SCIENTIFIC
Description:
Product Description6-Amino-1-methyluracil is an amino derivative of uracil and its standard molar enthalpy of combustion has been evaluated. Host-guest complexation of 6-amino-1-methyluracil with tetrapropoxycalix[4]arene has been reported.Product Application6-Amino-1-methyluracil may be used in the preparation of 1,1′-di methyl-1H-spiro[pyrimido[4,5-b]quinoline-5,5′-pyrrolo[2,3-d]pyrimidine]-2,2′,4,4′,6′(1′H,3H,3′H,7′H,1′H)-pentaone, via reaction with isatin in the presence of catalytic p-toluene sulfonic acid.
Catalog Number:
(10407-398)
Supplier:
Bioss
Description:
The CYP39A1 gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of steroids, cholesterol and other lipids. This endoplasmic reticulum protein is involved in the conversion of cholesterol to bile acids. Its substrates include the oxysterols 25-hydroxycholesterol, 27-hydroxycholesterol and 24-hydroxycholesterol.
Catalog Number:
(10407-396)
Supplier:
Bioss
Description:
The CYP39A1 gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of steroids, cholesterol and other lipids. This endoplasmic reticulum protein is involved in the conversion of cholesterol to bile acids. Its substrates include the oxysterols 25-hydroxycholesterol, 27-hydroxycholesterol and 24-hydroxycholesterol.
Catalog Number:
(101920-358)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 060623-500MG , MDL Number: MFCD18071338
Catalog Number:
(10109-150)
Supplier:
Prosci
Description:
DECR2 is auxiliary enzyme of beta-oxidation. It participates in the degradation of unsaturated fatty enoyl-CoA esters having double bonds in both even- and odd-numbered positions in peroxisome. It catalyzes the NADP-dependent reduction of 2,4-dienoyl-CoA to yield trans-3-enoyl-CoA and has activity towards short and medium chain 2,4-dienoyl-CoAs, but also towards 2,4,7,10,13,16,19-docosaheptaenoyl-CoA, suggesting that it does not constitute a rate limiting step in the peroxisomal degradation of docosahexaenoic acid.
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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
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
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