You Searched For: (2-Methoxyphenyl)acetonitrile


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Description: Advanced airflow technology makes this the most energy efficient compressed air filtration system available.
Catalog Number: MFLX29587-11
UOM: 1 * 1 items
Supplier: Avantor Fluid Handling


Description: Parker Domnick Hunter hydrogen generators produce a continuous flow of pure hydrogen from deionised water. These hydrogen generators provide a safe and hassle-free alternative to high pressure gas cylinders. Hydrogen is only generated on demand at low pressure and the volume of stored gas is minimal.
Catalog Number: DHUN110H-MDCARRIER
UOM: 1 * 1 items
Supplier: DOMNICK HUNTER

New Product


Description: Maintenance kit 4000 hours for all LC-MS
Catalog Number: 564-0006
UOM: 1 * 1 items
Supplier: DOMNICK HUNTER


Description: This sulpho-SHPP (water-soluble Bolton-Hunter Reagent) is designed to aid the labelling of proteins with radioactive iodine. Radioactive iodine (¹²⁵I) is routinely used by researchers to label proteins. The iodination of proteins can be performed enzymatically or chemically.
Catalog Number: BC92
UOM: 1 * 100 mg
Supplier: G-Biosciences


Description: Bolton-Hunter reagent (sulpho-SHPP)
Catalog Number: APOSBII101-1G
UOM: 1 * 1 g
Supplier: Apollo Scientific


Description: Bolton-Hunter reagent (sulpho-SHPP), Technical Grade
Catalog Number: APOSBII110-5G
UOM: 1 * 5 g
Supplier: Apollo Scientific


Description: Bolton-Hunter reagent (sulpho-SHPP)
Catalog Number: J64508.03
UOM: 1 * 1 g
Supplier: Thermo Fisher Scientific

Description: Sulpho-SHPP, sulphosuccinimidyl-3 -(4-hydroxypheynyl) propionate, also known as water-soluble Bolton-Hunter reagent, conjugates tyrosine-like functional groups to primary amines to increase the number of tyrosyl groups that can be iodinated by iodine-125 labeling procedures.
Catalog Number: PIER27712
UOM: 1 * 100 mg
Supplier: Thermo Fisher Scientific


Description: Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.
Catalog Number: BOSSBS-6580R-HRP
UOM: 1 * 100 µl
Supplier: Bioss


Description: Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.
Catalog Number: BOSSBS-6580R
UOM: 1 * 100 µl
Supplier: Bioss


Description: Splinter forceps with lancet tips.
Catalog Number: 232-0063
UOM: 1 * 1 items
Supplier: HAMMACHER KARL


Description: The protein encoded by this gene is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. This group of proteins is characterized by a polybasic proteolytic processing site which is cleaved to produce a mature protein containing seven conserved cysteine residues. The members of this family are regulators of cell growth and differentiation in both embryonic and adult tissues. Mutations in this gene are associated with acromesomelic dysplasia, Hunter-Thompson type; brachydactyly, type C; and chondrodysplasia, Grebe type. These associations confirm that the gene product plays a role in skeletal development.
Catalog Number: PRSI56-193
UOM: 1 * 400 µl
Supplier: ProSci Inc.

New Product


Description: Interleukin 6 receptor (IL-6R) alpha is a type I transmembrane glycoprotein that forms a complex with type I transmembrane signal transducer protein gp130 (CD130) and mediates the biological activities of IL-6. IL-6 binds to the membrane-bound non-signaling IL-6R alpha (mIL-6R), and the complex binds to two molecules of gp130 and leads to ‘classical’ IL-6-signal transduction, which includes activation of JAK/STAT, ERK, and PI3K signal transduction pathways (Scheller <i>et al.</i>). In contrast, a soluble form of IL-6R alpha (sIL-6R), which comprises the extracellular portion of the receptor, binds to the secreted IL-6 to form a complex that promotes bioavailability of IL-6. The complex of IL-6 and sIL-6R can bind to gp130 on cells that do not express the IL-6R and are unresponsive to IL-6. This process is known as trans-signaling (Hunter and Jones; Rose-John S). sIL-6R regulates both local and systemic IL-6-mediated events. Elevated levels of sIL-6R have been documented in several disease conditions such as rheumatoid arthritis, myeloma, and Crohn’s disease (Jones <i>et al.</i>; Mihara <i>et al.</i>).
Catalog Number: STMC78083.1
UOM: 1 * 50 µG
Supplier: STEMCELL Technologies


Description: A series of spectrophotometric colorimeters for colour grading of optically clear samples. Each version of the PFX<i>i </i>195 includes a selection of standard colour scales that is used in a specific industry sector. Additional scales can be added, at the time of order or remotely, as optional upgrades, to provide the flexibility to meet individual requirements. Results can also be displayed in terms of spectral data and CIE values. For product types that are incompatible with the standard colour scales, the PFX<i>i </i>195 software allows the users to build up a customised scale from a series of reference samples, and then to obtain the closest match to the stored reference.
Catalog Number: 633-0221
UOM: 1 * 1 items
Supplier: Lovibond Tintometer


Description: It is well known that the control of gene expression involves activation of protein kinase cascades that regulate transcription factors within the nucleus (Karin and Hunter, 1995). The cyclic AMP response element binding protein (CREB) is one of the best characterized stimulus-induced transcription factors (Montminy, 1997). This transcription factor is a component of intracellular signaling events that regulate a wide range of biological functions, from spermatogenesis to circadian rhythms and memory (Shaywitz and Greenberg, 1999; Silva et al., 1998). A variety of protein kinases including protein kinase A (PKA), mitogenactivated protein kinases (MAPKs), and Ca2+/calmodulin-dependent protein kinases (CaMKs) phosphorylate CREB at serine 133 (Ser133), and phosphorylation of Ser133 are required for CREB-mediated transcription (Johannessen et al., 2004; Kornhauser et al., 2002).
Catalog Number: PRSI50-221
UOM: 1 * 100 µl
Supplier: ProSci Inc.


Description: 3M PELTOR ProTac Hunter Headset, green, headband 1 * 1 items
Catalog Number: MMMAMT13H222A
UOM: 1 * 1 items
Supplier: 3M


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