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chromatography+columns+HyClone+products+(Cytiva)
Catalog Number:
(10101-864)
Supplier:
Prosci
Description:
ZNF619 belongs to the krueppel C2H2-type zinc-finger protein family. It contains 10 C2H2-type zinc fingers. ZNF619 may be involved in transcriptional regulation.
Catalog Number:
(10102-052)
Supplier:
Prosci
Description:
ZNF192 belongs to the krueppel C2H2-type zinc-finger protein family and contains the conserved SCAN box domain. ZNF192 may be involved in transcriptional regulation.
Supplier:
AGILENT TECHNOLOGIES, INC (CSD) CA
Description:
Pistons and seals designed to ensure your pump delivers the best performance.
Catalog Number:
(10110-422)
Supplier:
Prosci
Description:
ZNF618 belongs to the krueppel C2H2-type zinc-finger protein family. It contains 4 C2H2-type zinc fingers. ZNF618 may be involved in transcriptional regulation.
Catalog Number:
(89298-060)
Supplier:
Genetex
Description:
Goat polyclonal antibody to BAF57 / SMARCE1
Supplier:
DWK Life Sciences (KIMBLE)
Description:
Polyethylene CapFor 1 x 3 in. Tanks Cylindrical glass tanks for the development of 1 x 3 in. plates. These tanks provide maximum vapor phase saturation with a minimum amount of solvent.
Supplier:
TRITON PRODUCTS TE
Description:
The DuraHook® shelf provides a lifetime of dependable service with commercial holding capacity.
Catalog Number:
(10082-400)
Supplier:
Proteintech
Description:
VVery long-chain acyl-CoA dehydrogenase (VLCAD) is one of four flavoproteins which catalyze the initial step of the mitochondrial b-oxidation spiral. It belongs to the acyl-CoA dehydrogenase family and is a homodimer of a 71-kDa polypeptide which contains 2 mol of FAD/mol of enzyme. The molecular mass of the nondenatured trypsinized VLCAD is 98 kDa, by gel filtration chromatography, indicating that it is a homodimer of the 48 kDa(tryptic digest) polypeptide. Defects in ACADVL are the cause of acyl-CoA dehydrogenase very long chain deficiency (ACADVLD). It has 2 isoforms(70 kDa and 68 kDa ) produced by alternative splicing and a transit peptide. This antibody is speicifc to ACADVL.
Catalog Number:
(89297-000)
Supplier:
Genetex
Description:
Goat polyclonal antibody to GLuR5 / GRIK1
Catalog Number:
(10090-934)
Supplier:
Proteintech
Description:
PAX1, also named as HUP48, is a transcriptional activator. It may play a role in the formation of segmented structures of the embryo and may play an important role in the normal development of the vertebral column. It is a marker of the sclerotomal compartment. PAX1 was reported that, quantitative measurement of PAX1 hyper-methylation in cervical scrapings is highly sensitive and is more specific than HC2 in detection of cervical cancer. It is expressed by vSMC and pericytes during the earliest phases of vascular wall formation. This antibody is specific to PAX1.
Catalog Number:
(10749-666)
Supplier:
Prosci
Description:
TSC1 Antibody: Tuberous sclerosis complex (TSC) is an autosomal dominant tumor syndrome caused by mutations in either of the TSC1 or TSC2 tumor suppressor genes. The products of these genes form a protein complex that indirectly decreases the signaling of the mammalian Target of Rapamycin (TOR), an evolutionarily conserved serine/threonine kinase that regulates cell growth and cell cycle through its ability to integrate signals from nutrient levels and growth factors. TOR activity is stimulated by Rheb, a member of the Ras superfamily of G-proteins, when the GTP/GDP ratio bound to Rheb is high. Immunoprecipitated TSC1/TSC2 has been shown to stimulate Rheb GTPase activity in vitro, suggesting that the TSC1/TSC2 decreases the ability of Rheb to stimulate TOR activity. This is supported by experiments showing overexpression of TSC1 and TSC2 results in a significant decrease in the GTP/GDP ratio bound to Rheb and the inhibition of cell growth. A shorter 40 kDa isoform of TSC1 has been shown to exist but its function is unknown.
Catalog Number:
(10459-158)
Supplier:
Bioss
Description:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
Supplier:
Omega Bio-Tek
Description:
Isolate DNA from up to 10 ml blood using magnetic beads.
Supplier:
New England Biolabs (NEB)
Description:
The EpiMark N6-Methyladenosine Enrichment Kit contains a rabbit monoclonal antibody specific for N6-Methyladenosine (m6A).
Supplier:
IBI Scientific
Description:
Supplemental kit for IBI Tri-Isolate RNA Pure Kit when working with bacterial cells.
Catalog Number:
(10099-964)
Supplier:
Prosci
Description:
DRGX is a transcription factor required for the formation of correct projections from nociceptive sensory neurons to the dorsal horn of the spinal cord and normal perception of pain.
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