You Searched For: AAL-993

Supplier: ENZO LIFE SCIENCES

Description: Highly potent inhibitor of VEGFR-1 (IC50=130nM), VEGFR-2 (IC50=23nM) and VEGFR-3 (IC50=18nM). At higher concentrations it inhibits PDGFR-β (640nM), c-Kit (236nM) and CSF-1R (380nM).

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Supplier: Thermo Scientific

Description: Manganese ≥99.3% (metals basis), powder -325 mesh

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Supplier: Thermo Scientific

Description: Ethylene glycol monomethyl ether (2-methoxyethanol) ≥99.3% ACS

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Supplier: VWR Chemicals

Description: SPECTRONORM solvents have extensive specifications to meet the highly demanding requirements of UV applications.

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Supplier: Thermo Scientific

Description: Barium bromide dihydrate ≥99.3%

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Catalog Number: (216-2304)

Supplier: Thermo Fisher Scientific

Description: These certified platinum clean HDPE bottles and carboys help reduce the potential for carry-over contamination in biopharmaceutical and vaccine productions.

UOM: 1 * 72 items

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Supplier: Apollo Scientific

Description: Trimethylsilane 99.99%

Catalog Number: (135-1882)

Supplier: asecos

Description: Storage cabinet accessories, Interior equipment: shelf in galvanised sheet steel: 993×492×30 mm (W×D×H) ; load capacity: 100 kg

UOM: 1 * 1 items

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Supplier: Merck

Description: LiChrosolv® hypergrade is accurately tested for LC-MS suitability, and meet all the requirements of modern LC-MS ionization methods (ESI/APCI - positive and negative mode).

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Supplier: Thermo Scientific

Description: Nickel(II) chloride hexahydrate ≥99.3% (metals basis)

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Catalog Number: (MSGA30520)

Supplier: asecos

Description: Storage cabinet accessories, sheet steel powder-coated shelf, 993×492×30 mm

UOM: 1 * 1 items

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Supplier: Thermo Scientific

Description: Strontium zirconium oxide ≥99.3% (metals basis)

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Supplier: Thermo Scientific

Description: Urea ≥99.3%

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Catalog Number: (BOSSBS-12317R)

Supplier: Bioss

Description: SCUBE3 is a novel secreted 993 amino acid cell-surface osteoblast protein that plays an important role in bone cell biology. While highly expressed in osteoblasts, SCUBE3 expression is unobservable or very low in non-bone tissues. SCUBE3 forms homo-oligomers and hetero-oligomers with SCUBE1, and may undergo C-terminal proteolytic cleavage or become N-glycosylated following translation. Two SCUBE3 isoforms exist as a result of alternative splicing events. SCUBE3 contains one CUB domain and nine EGF-like domains, and is encoded by a gene which maps to human chromosome 6p21.31, a region associated with a rare form of metabolic bone disease known as Paget's disease. Chromosome 6 contains 170 million base pairs and comprises nearly 6% of the human genome.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-11757R-A750)

Supplier: Bioss

Description: IGHMBP2 is a 993 amino acid nuclear and cytoplasmic protein that is ubiquitously expressed. Belonging to the DNA2/NAM7 helicase family, IGHMBP2 is a 5' to 3' helicase that unwinds RNA and DNA duplexes in an ATP-dependent reaction. IGHMBP2 also acts as a transcriptional regulator and is necessary for transcriptional activation of the flounder liver-type antifreeze protein gene. IGHMBP2 exists as a homooligomer and is part of the cytosolic ribonucleoprotein complex. Mutations in the gene encoding IGHMBP2 are suggested to lead to distal hereditary motor neuronopathy type 6 (HMN6), also known as spinal muscular atrophy distal autosomal recessive 1 (DSMA1) or spinal muscular atrophy with respiratory distress 1 (SMARD1). HMN6 is characterised by weakness and wasting of distal muscles of the anterior tibial and peroneal compartments of the legs and severe respiratory distress.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-11757R-CY7)

Supplier: Bioss

Description: IGHMBP2 is a 993 amino acid nuclear and cytoplasmic protein that is ubiquitously expressed. Belonging to the DNA2/NAM7 helicase family, IGHMBP2 is a 5' to 3' helicase that unwinds RNA and DNA duplexes in an ATP-dependent reaction. IGHMBP2 also acts as a transcriptional regulator and is necessary for transcriptional activation of the flounder liver-type antifreeze protein gene. IGHMBP2 exists as a homooligomer and is part of the cytosolic ribonucleoprotein complex. Mutations in the gene encoding IGHMBP2 are suggested to lead to distal hereditary motor neuronopathy type 6 (HMN6), also known as spinal muscular atrophy distal autosomal recessive 1 (DSMA1) or spinal muscular atrophy with respiratory distress 1 (SMARD1). HMN6 is characterized by weakness and wasting of distal muscles of the anterior tibial and peroneal compartments of the legs and severe respiratory distress.

UOM: 1 * 100 µl

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