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Catalog Number: (10471-686)
Supplier: Bioss
Description: The protein encoded by this gene is a member of the S100family of proteins containing 2 EF-hand calcium-binding motifs.S100 proteins are localized in the cytoplasm and/or nucleus of awide range of cells, and involved in the regulation of a number ofcellular processes such as cell cycle progression anddifferentiation. S100 genes include at least 13 members which arelocated as a cluster on chromosome 1q21. This protein may have atumor suppressor function. Chromosomal rearrangements and alteredexpression of this gene have been implicated in breast cancer.


Supplier: Ansell Healthcare
Description: Designed for critical cleanroom environments.
Supplier: Excelta
Description: Cobalt alloy tweezers were specifically designed for work under a microscope and engineered to fit small hands.

Small Business Enterprise Minority or Woman-Owned Business Enterprise

Supplier: Ansell Healthcare
Description: Goatskin leather protectors, for enhanced low-voltage glove life and improved hand safety. Designed to be worn over Class 0 and 00 electrical safety gloves, these leather protectors can significantly extend wear life.

Supplier: MCR Safety
Description: Kevlar® string knit gloves are used for general purpose work applications to provide cut and abrasion resistance, using high performance yarns, to further protect the hands when working with sharp objects.

Supplier: Electron Microscopy Sciences
Description: The stainless steel rectangular blocks are a useful tool for a number of tasks. These blocks also serve as a convenient hand held flat freezing surface useful in gently cooling the tissue without the use of sprays and in plastering technique.

Supplier: WORLD PRECISION INSTRUMENTS LLC
Description: Westcott student spring scissors are popular spring handled scissors that automatically reopen after each cut. Westcott brand spring scissors give you an ergonomic and comfortable grip, reducing hand strain and fatigue during repetitive cutting tasks.

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Supplier: Safety & Industrial Supplies
Description: Designed to be bolted to fixed ladders for hands-free protection while climbing and descending.

Catalog Number: (103288-280)
Supplier: Novus Biologicals
Description: The EFHD1 Antibody from Novus Biologicals is a rabbit polyclonal antibody to EFHD1. This antibody reacts with human. The EFHD1 Antibody has been validated for the following applications: Immunohistochemistry, Immunocytochemistry / Immunofluorescence, Immunohistochemistry-Paraffin.


Supplier: Brandtech
Description: Economical wiping seal dispenser that can handle many of the fluids used in biological labs

Catalog Number: (10451-142)
Supplier: Bioss
Description: On ligand binding, forms a receptor complex consisting of two type II and two type I transmembrane serine/threonine kinases. Type II receptors phosphorylate and activate type I receptors which autophosphorylate, then bind and activate SMAD transcriptional regulators. Receptor for BMP7/OP-1 and GDF5.Involvement in disease; Defects in BMPR1B are the cause of acromesomelic chondrodysplasia with genital anomalies (AMDGA). 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).Defects in BMPR1B are a cause of brachydactyly type A2 (BDA2) [MIM:112600]. Brachydactylies (BDs) are a group of inherited malformations characterized by shortening of the digits due to abnormal development of the phalanges and/or the metacarpals. They have been classified on an anatomic and genetic basis into five groups, A to E, including three subgroups (A1 to A3) that usually manifest as autosomal dominant traits. BDA2 was described first in a large Norwegian kindred. BDA2 is caused by mutations in BMPR1B gene and studies demonstrate that these mutations function as dominant negatives in vitro and in vivo.


Catalog Number: (10100-826)
Supplier: Prosci
Description: PAX3 is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. Mutations in paired box gene 3 are associated with Waardenburg syndrome, craniofacial-deafness-hand syndrome, and alveolar rhabdomyosarcoma. The translocation t (2;13) (q35;q14), which represents a fusion between PAX3 and the forkhead gene, is a frequent finding in alveolar rhabdomyosarcoma.This gene is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. Mutations in paired box gene 3 are associated with Waardenburg syndrome, craniofacial-deafness-hand syndrome, and alveolar rhabdomyosarcoma. The translocation t (2;13) (q35;q14), which represents a fusion between PAX3 and the forkhead gene, is a frequent finding in alveolar rhabdomyosarcoma. Alternative splicing results in transcripts encoding isoforms with different C-termini.


Supplier: RUDIGER ANATOMIE GMBH
Description: A Complete, Unassembled, Life Size Skeleton.

Supplier: Atago
Description: ATAGO offers its “Palette” series digital refractometers for a wide range of applications and industries

Catalog Number: (470163-834)
Supplier: NEWPATH LEARNING LLC
Description: A Great Classroom Solution.


Supplier: Wells Lamont
Description: Thin, conformable nylon glove liners provide excellent fit, feel, and comfort.

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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 call 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 call is still displayed and you need assistance, please call us at 1-800-932-5000.
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