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Pyrazine-2-carboximidamide+hydrochloride
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Pyrazine-2-carboximidamide+hydrochloride
Supplier:
AOB CHEM USA
Description:
1-Bromo-4-((4-Bromobenzyl)oxy)-2-methoxybenzene ≥97%
Catalog Number:
(10672-078)
Supplier:
Bioss
Description:
Tripartite motif-containing protein 3 (TRIM3), also known as RING finger protein 22 (RNF22), RING finger protein 97 (RNF97) or brain-expressed RING finger protein (BERP), is a 744 amino acid member of the TRIM family, also known as the RING-B-box coiled-coil (RBCC) family. Members of the RBCC family have an N-terminal RING finger, followed by one or two zinc-binding domains (B-box domains), a leucine coiled-coil region and a variable C-terminal domain. Localized to cytoplasmic filaments, TRIM3 has been shown to interact with å-actinin-4 and myosin V, two proteins associated with the actin cytoskeleton. Specifically, å-actinin-4 interacts with the RBCC domain of TRIM3, and the C-terminal tail of Myosin V interacts with with the unique C-terminal ∫-propeller domain of TRIM3. These associations suggest that TRIM3 may play a role in cell motility and cargo transport. Three named isoforms of TRIM3 exist as a result of alternative splicing events.
Supplier:
AMBEED, INC
Description:
(S)-tert-Butyl 3-((methylsulfonyl)oxy)piperidine-1-carboxylate, Purity: 95%, CAS Number: 940890-90-4, Appearance: White to Yellow Solid, Storage: Sealed in dry, 2-8 C, Size: 1g
Catalog Number:
(76120-460)
Supplier:
Bioss
Description:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases and encodes nearly 900 genes. Considered 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, and familial dysautonomia are associated with chromosome 9. Also, chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 050274-500MG , MDL Number: MFCD13560675
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 050366-500MG , MDL Number: MFCD13560767
Catalog Number:
(101815-214)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 023032-500MG , MDL Number: MFCD12026497
Catalog Number:
(101815-264)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 023057-500MG , MDL Number: MFCD12026498
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 049623-500MG , MDL Number: MFCD13560025
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 045243-5G , MDL Number: MFCD00173481
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 045847-500MG , MDL Number: MFCD00202691
Catalog Number:
(76099-538)
Supplier:
Bioss
Description:
C9orf5 (chromosome 9 open reading frame 5), also known as CG2, is a 911 amino acid multi-pass membrane protein that is widely expressed and exists as four alternatively spliced isoforms. The gene encoding C9orf5 maps to human chromosome 9, which consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Considered 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.
Supplier:
AMBEED, INC
Description:
8-(((2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one, Purity: 97%, CAS: 76135-82-5, Appearance: Light-yellow powder, Size: 5mg
Supplier:
Thermo Scientific Chemicals
Description:
MDL: MFCD00064340
Beilstein Registry No.: 86197
Optical Rotation: -31.5°C (c=1 in water)
Catalog Number:
(80109-738)
Supplier:
MilliporeSigma
Description:
A boronic acid-based, reversible proteasome inhibitor that is structurally similar to MG-132 (80053-194, -196) but displays much higher potency (Ki=0.03nM vs)
Catalog Number:
(10298-582)
Supplier:
Bioss
Description:
This gene encodes a G-protein beta-subunit-like polypeptide which is a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene. [provided by RefSeq, Jul 2008].
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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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