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Product Image-CA101418-182

PspOMI

Description: An E.coli strain that carries the cloned PspOMI gene from Pseudomonas species OM2164, (S.K. Degtyarev).
Catalog Number: CA101418-182
Supplier: New England Biolabs (NEB)
Product Image-CA101444-796

Hpy166II

Description: An E. coli strain that carries the cloned Hpy166II gene from Helicobacter pylori J166 (M.J. Blaser).
Catalog Number: CA101444-796
Supplier: New England Biolabs (NEB)
Image Unavailable-CA610-9502

Anti-IgG Chicken Polyclonal Antibody (AP (Alkaline Phosphatase))

Description: Secondary Chicken Anti-IgG (H&L) Reacts with Mouse
Catalog Number: CA610-9502
Supplier: Rockland Immunochemical
Image Unavailable-55407-226

Accessories for Photometry Reagents for 9000 Series Photometers, YSI

Description: Replacement reagent starter kit for Model 9000 Series Portable Photometers (55407-052, -054, and -056). Includes accessories for 250 tests. Indefinite shelf life. No calibration from test to test or lot to lot required. Range: 0-100mg/L.
Catalog Number: 55407-226
Supplier: YSI

SDS


Product Image-CA76284-680

Thermostable RNase H

Description: Thermostable RNase H is an endoribonuclease that is functional at high temperatures and selectively hydrolyzes the phosphodiester bonds of an RNA strand in an RNA:DNA hybrid molecule, while leaving the DNA strand intact.
Catalog Number: CA76284-680
Supplier: New England Biolabs (NEB)
Product Image-10089-264

Anti-KIR2.1 Rabbit Polyclonal Antibody

Description: KCNJ2, also named as HHBIRK1, HHIRK1, IRK1, KIR2.1, LQT7 and SQT3, belongs to the inward rectifier-type potassium channel family. KCNJ2 probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. KCNJ2 can be blocked by extracellular barium or cesium. Defects in KCNJ2 are the cause of long QT syndrome type 7 (LQT7). Defects in KCNJ2 are the cause of short QT syndrome type 3 (SQT3). The antibody recognizes the C-term of KCNJ2.
Catalog Number: 10089-264
Supplier: Proteintech
Product Image-CA102877-822

WARMSTART® RTx Reverse Transcriptase, New England Biolabs

Description: WarmStart RTx Reverse Transcriptase is a unique in silico designed RNA-directed DNA polymerase coupled with a reversibly-bound aptamer that inhibits RTx activity below 40°C
Catalog Number: CA102877-822
Supplier: New England Biolabs (NEB)
Image Unavailable-CA612-1503

Anti-IgG Goat Polyclonal Antibody (AP (Alkaline Phosphatase))

Description: Secondary Goat Anti-IgG F(c) Reacts with Rat
Catalog Number: CA612-1503
Supplier: Rockland Immunochemical
Product Image-CA101418-186

PspXI

Description: An E.coli strain that carries the cloned PspXI gene from Pseudomanas species A1-1 (S.K. Degtyarev).
Catalog Number: CA101418-186
Supplier: New England Biolabs (NEB)
Image Unavailable-10479-706

Anti-FAHD2A Rabbit Polyclonal Antibody

Description: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
Catalog Number: 10479-706
Supplier: Bioss
Image Unavailable-10479-758

Anti-FAHD2A Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Description: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
Catalog Number: 10479-758
Supplier: Bioss
Image Unavailable-10479-756

Anti-FAHD2A Rabbit Polyclonal Antibody (Cy7®)

Description: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
Catalog Number: 10479-756
Supplier: Bioss
Product Image-CA101444-720

LONGAMP® Taq PCR Kit, New England Biolabs

Description: The LongAmp Taq PCR Kit features LongAmp Taq DNA Polymerase, which is a unique blend of Taq and Deep VentR ™ DNA Polymerases
Catalog Number: CA101444-720
Supplier: New England Biolabs (NEB)
Product Image-CA102902-462

BssSI-v2

Description: An E.coli strain that carries the cloned and modified BssSI gene from Bacillus stearothermophilus S719 (Z. Chen).
Catalog Number: CA102902-462
Supplier: New England Biolabs (NEB)
Image Unavailable-CA607-1502

Anti-IgG Goat Polyclonal Antibody (AP (Alkaline Phosphatase))

Description: Secondary Goat Anti-IgG (H&L) Reacts with Hamster
Catalog Number: CA607-1502
Supplier: Rockland Immunochemical
Image Unavailable-75977-370

Anti-TOP1MT Mouse Monoclonal Antibody (CF647) [clone: TOP1MT/488]

Description: DNA topoisomerases are nuclear enzymes that regulate the topological structure of DNA in eukaryotic cells by transiently breaking and rejoining DNA strands. Due to their roles in DNA replication, recombination, and transcription, DNA topoisomerases have been identified as targets of numerous anticancer drugs. Mitochondrial Topo I (DNA topoisomerase I, mitochondrial) is a 601 amino acid protein that primarily acts to relieve DNA strain that may occur during duplication of mitochondrial DNA. As a type IB topoisomerase, mitochondrial Topo I requires a divalent metal, either, calcium or magnesium, as well as an alkaline pH for optimal activity.

CF® dyes are Biotium's next-generation fluorescent dyes. CF®647 is a far-red fluorescent dye (Ex/Em 650/665 nm) with excellent brightness. It also is compatible with super-resolution imaging by STORM.
Catalog Number: 75977-370
Supplier: Biotium
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