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(2S,2'S)-2,2'-(Hexadecanedioylbis(azanediyl))dipentanedioic+acid


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Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 036897-500MG , MDL Number: MFCD07365349
Supplier:  AMBEED, INC
Description:   4-Hydroxy-3-methoxyphenylboronic acid pinacol ester 98%
Supplier:  AMBEED, INC
Description:   5-(2-(tert-Butyl)-4-(4-fluorophenyl)-1H-imidazol-5-yl)-3-neopentyl-3H-imidazo[4,5-b]pyridin-2-amine dimethanesulfonate, Purity: 98+%, CAS Number: 862507-23-1, Appearance: Light yellow to yellow powder or crystals, Storage: Inert atmosphere, Room Temperature, Size: 1mg
Supplier:  Matrix Scientific
Description:   4-(4-Methylphenyl)-1H-pyrrole-3-carboxylic acid ≥97%
Catalog Number: (10481-618)

Supplier:  Bioss
Description:   ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
Supplier:  MP Biomedicals
Description:   Essential vitamin that is important for amino acid and energy metabolism, and fatty acid synthesis. It is a prosthetic group in four mammalian carboxylase families and facilitates the binding and transfer of carbon dioxide.
MSDS SDS
Supplier:  APOLLO SCIENTIFIC
Description:   Glyoxylic acid monohydrate 97%

Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 027820-500MG , MDL Number: MFCD01993642

Supplier:  Bioss
Description:   C22orf37 (chromosome 22 open reading frame 37), also known as FLJ40542, is a 170 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
Supplier:  Bioss
Description:   ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
Catalog Number: (10099-754)

Supplier:  Prosci
Description:   SLC27A2 is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy.The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy.
Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 043268-5G , MDL Number: MFCD06659535
Supplier:  Invitrogen
Description:   Thermo Scientific Pierce Heptafluorobutyric Acid (HFBA) is manufactured and tested to meet strict specifications that ensure superior performance for use as an ion-pairing agent.
MSDS SDS
Supplier:  Biolegend
Description:   Recombinant Human FcER1A, Source: 293E cells, Reactivity: Human, Purity: >95%, Molecular Mass: 189 amino acid recombinant protein has a predicted molecular mass of approximately 22 kD, Application: Bioassay, Synonyms: FceR1a, FceR1-a, FceR1-alpha, FceR1 alpha, Size: 25 ug
Supplier:  AMBEED, INC
Description:   1-Azetidinecarboxylic acid-3-hydroxyphenylmethyl ester 97%
Catalog Number: (10113-314)

Supplier:  Prosci
Description:   Polyclonal, Host: Goat, Species Reactivity: Human, Immunogen: GOT1 antibody was raised against a 14 amino acid synthetic peptide near the internal region of GOT1 (aa 22-35), Tested Applications: ELISA, WB
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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 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.
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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.
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