You Searched For: HARRISON+SMITH+FRENCH+FLINT

Supplier: SEQENS

Description: SEQENS IVD manufactures Bovine Serum Albumin (BSA) derived from plasma, collected from healthy animals of French origin. This product is obtained by 'Heat Shock' method, which ensures higher purity and preserves BSA intrinsic properties.

Supplier: SEQENS

Description: This human pooled serum is obtained from off-the-clot serum units collected in France. Units are pooled and 0,2 μm filtered prior to being bottled. Possibility of gender and blood group selection.

Catalog Number: (PRSI90-069)

Supplier: ProSci Inc.

Description: Microfibril-associated protein 4 (MFAP4) was initially identified as a gene commonly deleted in the contiguous Smith-Magenis syndrome (SMS) gene. MFAP4 was identified as growth factor to support expansion of hematopoietic stem cells in culture. It is involved in calcium-dependent cell adhesion and intercellular interactions.

UOM: 1 * 50 µG

Catalog Number: (PRSI90-068)

Supplier: ProSci Inc.

Description: Microfibril-associated protein 4 (MFAP4) was initially identified as a gene commonly deleted in the contiguous Smith-Magenis syndrome (SMS) gene. MFAP4 was identified as growth factor to support expansion of hematopoietic stem cells in culture. It is involved in calcium-dependent cell adhesion and intercellular interactions.

UOM: 1 * 10 µG

Catalog Number: (PRSI25-254)

Supplier: ProSci Inc.

Description: KCNJ12 is an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). This gene is located within the Smith-Magenis syndrome region on chromosome 17. This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

UOM: 1 * 50 µG

Catalog Number: (PRSI28-009)

Supplier: ProSci Inc.

Description: ZNF179 encodes a member of the RING finger protein family of transcription factors. The protein is primarily expressed in brain. The gene is located within the Smith-Magenis syndrome region on chromosome 17.

UOM: 1 * 50 µG

Catalog Number: (PRSI26-828)

Supplier: ProSci Inc.

Description: The exact function of C17orf39 remains unknown.The multiprotein Mediator complex is a coactivator required for activation of RNA polymerase II transcription by DNA bound transcription factors. The protein encoded by this gene is thought to be a subunit of the Mediator complex. This gene is located within the Smith-Magenis syndrome region on chromosome 17.

UOM: 1 * 50 µG

Supplier: SMITH SCIENTIFIC

Description: Borosilicate glass.

Catalog Number: (PRSI91-687)

Supplier: ProSci Inc.

Description: Serine Hydroxymethyltransferase Cytosolic (SHMT1) is a member of the SHMT family. SHMT1 is a cytoplasmic protein and exists as a homotetramer. SHMT1 catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. This reaction provides one carbon unit for the synthesis of methionine, thymidylate, and purines in the cytoplasm. A reduction in SHMT1 levels would result in less glycine that could affect the nervous system by acting as an agonist to the NMDA receptor and this could be a mechanism behind Smith-Magenis syndrome.

UOM: 1 * 50 µG

Catalog Number: (PRSI25-511)

Supplier: ProSci Inc.

Description: ZNF287 is a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene encodes a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene is located near the Smith-Magenis syndrome region on chromosome 17.

UOM: 1 * 50 µG

Supplier: SMITH SCIENTIFIC

Description: Borosilicate glass.

Catalog Number: (PRSI92-386)

Supplier: ProSci Inc.

Description: Microfibril-associated glycoprotein 4(MFAP4) is a secreted protein and contains 1 fibrinogen C-terminal domain, similarity to a bovine microfibril-associated protein. The protein has binding specificities for both collagen and carbohydrate. It is thought to be an extracellular matrix protein which is involved in calcium-dependent cell adhesion or intercellular interactions. The gene is located within the Smith-Magenis syndrome region.

UOM: 1 * 50 µG

Catalog Number: (PRSIXP-5278)

Supplier: ProSci Inc.

Description: TACI is a lymphocyte specific member of the tumor necrosis factor (TNF) receptor superfamily. It interacts with calcium-modulator and cyclophilin ligand (CAML). The protein binds to both APRIL and BAFF and induces activation of the transcription factors NFAT (nuclear-factor of activated T cells), AP1, and NF kappa B and plays a crucial role in humoral immunity by interacting with a TNF ligand. This gene is located within the Smith Magenis syndrome region on chromosome 17.

UOM: 1 * 100 µG

Supplier: SMITH SCIENTIFIC

Description: Borosilicate glass.

New Product

Supplier: SMITH SCIENTIFIC

Description: Borosilicate glass 3.3, with plastic stopper.

Catalog Number: (PRSIXP-5278BT)

Supplier: ProSci Inc.

Description: TACI is a lymphocyte specific member of the tumor necrosis factor (TNF) receptor superfamily. It interacts with calcium-modulator and cyclophilin ligand (CAML). The protein binds to both APRIL and BAFF and induces activation of the transcription factors NFAT (nuclear-factor of activated T cells), AP1, and NF kappa B and plays a crucial role in humoral immunity by interacting with a TNF ligand. This gene is located within the Smith Magenis syndrome region on chromosome 17.

UOM: 1 * 50 µG