Ambient

Molecular Formula : C15 D6 H4 O6

Molecular Formula : C15 D6 H4 O6

Molecular Formula : C21 H18 O12

Molecular Formula : C21 H18 O12

Molecular Formula : C6 H12 O6

Molecular Formula : C6 H12 O6

Molecular Formula : C6 H12 O6

Molecular Formula : C6H6D6O6

Molecular Formula : C6H6D6O6

Dropout formulation of synthetic defined (SDA) yeast medium (without Leucine) with agar includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

Dropout formulation of synthetic defined (SDA) yeast medium (without Adenine, Histidine, Leucine and Tryptophan) with Agar includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

SD Media (Pack)(Pouches)

SD Media (Pack)(Pouches)

SD medium Leu-Ura

Dropout formulation of synthetic defined (SD) yeast medium (without Adenine, Histidine, Leucine and Tryptophan) includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

Dropout formulation of synthetic defined (SD) yeast medium (without Adenine, Histidine, Leucine and Tryptophan) includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

Dropout formulation of synthetic defined (SD) yeast medium (without Histidine, Leucine and Tryptophan) includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

Dropout formulation of synthetic defined (SD) yeast medium (without Histidine, Leucine and Tryptophan) includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

Dropout formulation of synthetic defined (SD) yeast medium (without Leucine) includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

Dropout SC aminoacid mixture formulation (without Uracil) for S. cerevisiae growth media. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes. Simply tear open the pouch and add to water

Dropout formulation of synthetic defined (SD) yeast medium (without Leucine and Tryptophan) includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

Dropout formulation of synthetic defined (SD) yeast medium (without Leucine and Tryptophan) includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

Dropout formulation of synthetic defined (SD) yeast medium (without Uracil) includes all necessary components for selective growth of Saccharomyces cerevisiae. Pre-measured, sealed pouches, for 0.5 L or 1 L batch sizes, simply tear open the pouch and add to water.

SDA Medium-His-Leu-Trp-Ura (PACK)(POUCHES)

SDA MEDIUM-LEU-TRP (PACK)(POUCHES)

SDA MEDIUM-LEU-TRP-URA (POWDER)

SDA MEDIUM-TRP (PACK) (POUCHES)

SDA Medium-Ura (pouches)

Stromal-Cell Derived Factor-1 alpha/ CXCL12 (SDF-1α) and SDF-1β, members of the chemokine α subfamily that lack the ELR domain, were initially identified using the signal sequence trap cloning strategy from a mouse bone-marrow stromal cell line. These proteins were subsequently also cloned from a human stromal cell line as cytokines that supported the proliferation of a stromal cell-dependent pre-B-cell line. SDF-1α and SDF-1β cDNAs encode precursor proteins of 89 and 93 amino acid residues, respectively. Both SDF-1α and SDF-1β are encoded by a single gene and arise by alternative splicing. The two proteins are identical except for the four amino acid residues that are present in the carboxy-terminus of SDF-1β and absent from SDF-1α. SDF-1/PBSF is highly conserved between species, with only one amino acid substitution between the mature human and mouse proteins. SDF-1/PBSF acts via the chemokine receptor CXCR4 and has been shown to be a chemoattractant for T-lymphocytes, monocytes, pro- and pre- B cells, but not neutrophils. Mice lacking SDF-1 or CXCR4 have been found to have impaired B-lymphopoiesis, myelopoiesis, vascular development, cardiogenesis and abnormal neuronal cell migration and patterning in the central nervous system.

Stromal-Cell Derived Factor-1 alpha/ CXCL12 (SDF-1α) and SDF-1β, members of the chemokine α subfamily that lack the ELR domain, were initially identified using the signal sequence trap cloning strategy from a mouse bone-marrow stromal cell line. These proteins were subsequently also cloned from a human stromal cell line as cytokines that supported the proliferation of a stromal cell-dependent pre-B-cell line. SDF-1α and SDF-1β cDNAs encode precursor proteins of 89 and 93 amino acid residues, respectively. Both SDF-1α and SDF-1β are encoded by a single gene and arise by alternative splicing. The two proteins are identical except for the four amino acid residues that are present in the carboxy-terminus of SDF-1β and absent from SDF-1α. SDF-1/PBSF is highly conserved between species, with only one amino acid substitution between the mature human and mouse proteins. SDF-1/PBSF acts via the chemokine receptor CXCR4 and has been shown to be a chemoattractant for T-lymphocytes, monocytes, pro- and pre- B cells, but not neutrophils. Mice lacking SDF-1 or CXCR4 have been found to have impaired B-lymphopoiesis, myelopoiesis, vascular development, cardiogenesis and abnormal neuronal cell migration and patterning in the central nervous system.

Stromal-Cell Derived Factor-1 alpha/ CXCL12 (SDF-1α) and SDF-1β, members of the chemokine α subfamily that lack the ELR domain, were initially identified using the signal sequence trap cloning strategy from a mouse bone-marrow stromal cell line. These proteins were subsequently also cloned from a human stromal cell line as cytokines that supported the proliferation of a stromal cell-dependent pre-B-cell line. SDF-1α and SDF-1β cDNAs encode precursor proteins of 89 and 93 amino acid residues, respectively. Both SDF-1α and SDF-1β are encoded by a single gene and arise by alternative splicing. The two proteins are identical except for the four amino acid residues that are present in the carboxy-terminus of SDF-1β and absent from SDF-1α. SDF-1/PBSF is highly conserved between species, with only one amino acid substitution between the mature human and mouse proteins. SDF-1/PBSF acts via the chemokine receptor CXCR4 and has been shown to be a chemoattractant for T-lymphocytes, monocytes, pro- and pre- B cells, but not neutrophils. Mice lacking SDF-1 or CXCR4 have been found to have impaired B-lymphopoiesis, myelopoiesis, vascular development, cardiogenesis and abnormal neuronal cell migration and patterning in the central nervous system.

Stromal-Cell Derived Factor-1 alpha/ CXCL12 (SDF-1α) and SDF-1β, members of the chemokine α subfamily that lack the ELR domain, were initially identified using the signal sequence trap cloning strategy from a mouse bone-marrow stromal cell line. These proteins were subsequently also cloned from a human stromal cell line as cytokines that supported the proliferation of a stromal cell-dependent pre-B-cell line. SDF-1α and SDF-1β cDNAs encode precursor proteins of 89 and 93 amino acid residues, respectively. Both SDF-1α and SDF-1β are encoded by a single gene and arise by alternative splicing. The two proteins are identical except for the four amino acid residues that are present in the carboxy-terminus of SDF-1β and absent from SDF-1α. SDF-1/PBSF is highly conserved between species, with only one amino acid substitution between the mature human and mouse proteins. SDF-1/PBSF acts via the chemokine receptor CXCR4 and has been shown to be a chemoattractant for T-lymphocytes, monocytes, pro- and pre- B cells, but not neutrophils. Mice lacking SDF-1 or CXCR4 have been found to have impaired B-lymphopoiesis, myelopoiesis, vascular development, cardiogenesis and abnormal neuronal cell migration and patterning in the central nervous system.

Stromal-Cell Derived Factor-1 beta (SDF-1β), also known as SCYB12, PBSF and CXCL12, is an 8.3 kDa, heparin-binding member of the CXC (or alpha) family of chemokines and signal through the CXCR4 receptor. SDF-1α and β are reported to be monomers at neutral pH and physiologic ionic strength, On the cell surface, this may well facilitate SDF-1 interaction with its two receptors, CXCR4 and syndecan4. Heparin sulfate is known to protect SDF-1 from proteolysis, and CXCR4 exists constitutively as a dimer. Among its many functions, CXCL12 is known to influence lymphopoiesis, regulate patterning and cell number of neural progenitors, and promote angiogenesis (12, 13). It also enhances the survival of myeloid progenitor cells

Stromal-Cell Derived Factor-1 beta (SDF-1β), also known as SCYB12, PBSF and CXCL12, is an 8.3 kDa, heparin-binding member of the CXC (or alpha) family of chemokines and signal through the CXCR4 receptor. SDF-1α and β are reported to be monomers at neutral pH and physiologic ionic strength, On the cell surface, this may well facilitate SDF-1 interaction with its two receptors, CXCR4 and syndecan4. Heparin sulfate is known to protect SDF-1 from proteolysis, and CXCR4 exists constitutively as a dimer. Among its many functions, CXCL12 is known to influence lymphopoiesis, regulate patterning and cell number of neural progenitors, and promote angiogenesis (12, 13). It also enhances the survival of myeloid progenitor cells

SDS is an anionic detergent typically used to solubilize and denature proteins for electrophoresis. Most proteins bind SDS in a ratio of 1.4 grams SDS to 1 gram protein. The charges intrinsic to the protein become insignificant compared to the overall negative charge provided by the bound SDS.It is RNAse,DNAse, Protease free with an assay value of 20%.This solution is provided as a convenient ready-to-use firmat which eliminates the need to handle powdered SDS.

SDS Easy Solution (12%)

SDS-urea Buffer

SDS-urea Buffer

Molecular Formula : C24H20ClN3O

Molecular Formula : C24H20ClN3O

Molecular Formula : C24H20ClN3O

Molecular Formula : C22 H17 Cl F3 N O3

Molecular Formula : C22 H17 Cl F3 N O3

Molecular Formula : C10 H18 O4

Molecular Formula : C10 H18 O4