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6-Methylpyridine-2,3-dicarboxylic acid
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6-Methylpyridine-2,3-dicarboxylic acid
Catalog Number:
(80050-862)
Supplier:
MilliporeSigma
Description:
In 500mM NaCl, 150mM imidazole, 20mM Tris-HCl, 5 mM DTT, 1mM EDTA, 10% glycerol, 0.1% CHAPS, pH 7.9
Supplier:
Enzo Life Sciences
Description:
Cyclic hydroxylamine spin probe for<i> in vivo</i>, intraperitoneal and intravenous injections.
Catalog Number:
(PI24308)
Supplier:
Invitrogen
Description:
Pierce™ Hydrochloric acid solution, sequencing grade, is purified and packaged to ensure a ninhydrin-negative blank on hydrolysis
Supplier:
MP Biomedicals
Description:
Tetracycline is a broad spectrum polyketide antibiotic with clinical uses in treating bacterial infections such as Rocky Mountain spotted fever, typush fever, tick fevers, Q fever, and Brill-Zinsser disease and to treat upper respiratory infections and acne. It has been used in studies of multidrug resistance and potential side effects including acute pancreatitis.
Catalog Number:
(103194-038)
Supplier:
Aqua Solutions
Description:
Hydrochloric Acid in Methanol, 0.01 normal, N.I.S.T. Traceable, Components: Methanol, Hydrochloric Acid 36-38%, Form: Liquid, Colour: Clear, Pack Size: 4L
Catalog Number:
(76821-046)
Supplier:
AMBEED, INC
Description:
2,4,6-Trichloronicotinonitrile, Purity: 95%, CAS Number: 40381-91-7, Appearance: Solid, Storage: Inert atmosphere, 2-8C, Size: 250MG
Catalog Number:
(10352-084)
Supplier:
Bioss
Description:
Aurora A plays a role in cell cycle regulation during anaphase and/or telophase, in relation to the function of the centrosome/spindle pole region during chromosome segregation. Aurora A plays a key role during tumor development and progression and is overexpressed in many human cancers including breast, ovarian and colorectal. Aurora A is viewed as a potential target for anticancer drug treatment.Aurora B is a mitotic protein kinase that phosphorylates histone H3 (probably on Serine 10), behaves as a chromosomal passenger protein, and may regulate several stages of mitosis such as centrosome separation, chromosome segregation and cytokinesis. It localizes to the inner centromere region from prophase to anaphase. The Aurora kinases, members of the Ser/Thr protein kinase family, associate with microtubules during chromosome movement and segregation. Aurora kinase C may play a part in organizing microtubules in relation to the function of the centrosome/spindle pole during mitosis. This protein is localized to centrosome from anaphase to cytokinesis. Expression is limited to testis in normal cells. Elevated expression levels are seen only in a subset of cancer cells such as HepG2, HuH7 and HeLa cells. Aurora-C expression is maximum at M phase.
Supplier:
AMBEED, INC
Description:
(-)-Quinine hydrochloride ≥99%
Supplier:
Thermo Scientific Chemicals
Description:
Molecular Formula: Ga in 5% HNO3/tr. HCl
Physical Form: Liquid UN No.: 3264 MDL No.: MFCD00134045
Catalog Number:
(77692-326)
Supplier:
LGC STANDARDS
Description:
1-(Thiophen-2-yl)-2-methylaminopropane Hydrochloride (Methiopropamine Hydrochloride; MPA HCl) 1.0 mg/ml in Methanol (as free base), LoGiCal, LGC Standards
Catalog Number:
(10799-934)
Supplier:
Rockland Immunochemical
Description:
AKT2 Antibody detects AKT2 which is a component of the PI-3 kinase pathway and is activated by phosphorylation at Ser 473 and Thr 308. AKT is a cytoplasmic protein also known as Protein Kinase B (PKB) and rac (related to A and C kinases). AKT is a key regulator of many signal transduction pathways. AKT Exhibits tight control over cell proliferation and cell viability. Overexpression or inappropriate activation of AKT is noted in many types of cancer. AKT mediates many of the downstream events of PI 3-kinase (a lipid kinase activated by growth factors, cytokines and insulin). PI 3-kinase recruits AKT to the membrane, where it is activated by PDK1 phosphorylation. Once phosphorylated, AKT dissociates from the membrane and phosphorylates targets in the cytoplasm and the cell nucleus. AKT has two main roles: (i) inhibition of apoptosis; (ii) promotion of proliferation. Anti-AKT2 Antibody is ideal for investigators involved in Cell Signaling, Neuroscience, Signal Transduction research.
Supplier:
AMBEED, INC
Description:
3-Chloro-L-alanine hydrochloride 98%
Catalog Number:
(10261-356)
Supplier:
Bioss
Description:
SCA11 is a 1,244 amino acid protein that belongs to the protein kinase superfamily and the CK1 Ser/Thr protein kinase family. The SCA11 gene, comprising of 16 exons, produces a 5.6-kb transcript in which the longest open reading frame is 3,732 nucleotides. Defects in the SCA11 protein are the cause of the disorder spinocerebellar ataxia type 11 (SCA11). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. The SCA11 disorder is an autosomal dominant cerebellar ataxia (ADCA). It is a relatively benign, late-onset, slowly progressive neurologic disorder. The SCA11 protein has also been implicated in Alzheimer disease and in tangle formation. Existing as three alternatively spliced isoforms, the SCA11 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 15q15.2.
Catalog Number:
(10261-098)
Supplier:
Bioss
Description:
SCA11 is a 1,244 amino acid protein that belongs to the protein kinase superfamily and the CK1 Ser/Thr protein kinase family. The SCA11 gene, comprising of 16 exons, produces a 5.6-kb transcript in which the longest open reading frame is 3,732 nucleotides. Defects in the SCA11 protein are the cause of the disorder spinocerebellar ataxia type 11 (SCA11). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. The SCA11 disorder is an autosomal dominant cerebellar ataxia (ADCA). It is a relatively benign, late-onset, slowly progressive neurologic disorder. The SCA11 protein has also been implicated in Alzheimer disease and in tangle formation. Existing as three alternatively spliced isoforms, the SCA11 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 15q15.2.
Catalog Number:
(10318-492)
Supplier:
Bioss
Description:
C9orf96, also known as Protein kinase-like protein SgK071, is a 680 amino acid protein that belongs to the Ser/Thr protein kinase family of the protein kinase superfamily. There are three isoforms of C9orf96 that are produced as a result of alternative splicing events. The gene encoding C9orf96 maps to human chromosome 9, which consists of about 145 million bases and 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:
tert-Butyl 4-aminobutanoate hydrochloride, Purity: 98%, CAS Number: 58640-01-0, Appearance: White to light-yellow powder or crystals, Storage: Inert atmosphere, 2-8C, Size: 100G
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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.
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