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N\\\\\\\'-[1-Cyclobutylaminopropylidene]hydrazinecarboxylic+acid-
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N\\\\\\\'-[1-Cyclobutylaminopropylidene]hydrazinecarboxylic+acid-
Catalog Number:
(101826-278)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 028508-500MG , MDL Number: MFCD03422402
Catalog Number:
(101826-406)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 028572-500MG , MDL Number: MFCD01008627
Catalog Number:
(101826-246)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 028492-500MG , MDL Number: MFCD00589050
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 045414-5G , MDL Number: MFCD03425812
Catalog Number:
(10318-338)
Supplier:
Bioss
Description:
C9orf163 (chromosome 9 open reading frame 163) is a 203 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(10314-304)
Supplier:
Bioss
Description:
C9orf21 (chromosome 9 open reading frame 21) is a 226 amino acid protein that belongs to the UPF0308 family and is encoded by a gene that maps to human chromosome 9q22.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(103267-322)
Supplier:
Novus Biologicals
Description:
The DUSP22 Antibody from Novus Biologicals is a rabbit polyclonal antibody to DUSP22. This antibody reacts with human. The DUSP22 Antibody has been validated for the following applications: Western Blot, Immunohistochemistry, Immunocytochemistry / Immunofluorescence, Immunohistochemistry-Paraffin.
Catalog Number:
(76220-156)
Supplier:
TCI America
Description:
1,1,1,3,5,5,5-Heptamethyl-3-[(trimethylsilyl)oxy]trisiloxane, Purity: >97.0%(GC), CAS: 17928-28-8, MF: C10H30O3Si4, MW: 310.69, Synonyms: Methyltris(trimethylsiloxy)silane, Form: Clear, Colorless - Almost colorless, Size: 25ML
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 045067-5G , MDL Number: MFCD00974909
Catalog Number:
(101826-544)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 028639-500MG , MDL Number: MFCD03422473
Supplier:
AMBEED, INC
Description:
(S)-N4-(3-Chloro-4-fluorophenyl)-7-((tetrahydrofuran-3-yl)oxy)quinazoline-4,6-diamine 98%
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 044556-1G , MDL Number: MFCD03001268
Catalog Number:
(103274-824)
Supplier:
Novus Biologicals
Description:
The RBFA Antibody from Novus Biologicals is a rabbit polyclonal antibody to RBFA. This antibody reacts with human. The RBFA Antibody has been validated for the following applications: Immunohistochemistry, Immunohistochemistry-Paraffin.
Catalog Number:
(76012-140)
Supplier:
Prosci
Description:
Meningioma 1 (MN1) contains two sets of CAG repeats. It is disrupted by a balanced translocation (4;22) in a meningioma, and its inactivation may contribute to meningioma 32 pathogenesis.
Catalog Number:
(10664-998)
Supplier:
Bioss
Description:
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
Catalog Number:
(10665-112)
Supplier:
Bioss
Description:
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
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 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
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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