220 Results for: "44686"
Corrected to: 4,6,6
Anti-LRRC6 Rabbit Polyclonal Antibody
Supplier: Bioss
The leucine-rich repeat-containing protein 6 (LRRC6), also designated Leucine-rich testis-specific protein (LRTP), is a 466 amino acid protein that contains 3 LRR repeats and plays a role in spermatogenesis. The gene encoding LRRC6 maps to chromosome 8, which encodes approximately 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Chromosome 8 is also associated with Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.
Expand 1 Items
Acrylonitrile ≥99% stabilized
Supplier: BeanTown Chemical
CAS: 107-13-1; EC No: 203-466-5; MDL No: MFCD00001927; RTECS: AT5250000 UN No: UN1093; Haz Class: 3 (6.1); Packing Group: I Liquid; Linear Formula: CH2=CHCN; MW: 53.06 Melting Point: -83°; Boiling Point: 77°; Flash point: -5°C (23°F) Refractive Index: 1.391 Light Sensitive
Expand 3 Items
Anti-USP39 Mouse Monoclonal Antibody [clone: 4G11]
Supplier: Novus Biologicals
The USP39 Antibody (4G11) from Novus Biologicals is a mouse monoclonal antibody to USP39. This antibody reacts with human. The USP39 Antibody (4G11) has been validated for the following applications: Western Blot, ELISA.
Expand 1 Items
Anti-VIM Mouse Monoclonal Antibody [clone: 4F2E9]
Supplier: Abnova
Mouse monoclonal antibody raised against partial recombinant VIM.
Expand 1 Items
Anti-CTDSPL2 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Supplier: Bioss
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
Expand 1 Items
Anti-LRRC6 Rabbit Polyclonal Antibody (Cy5®)
Supplier: Bioss
The leucine-rich repeat-containing protein 6 (LRRC6), also designated Leucine-rich testis-specific protein (LRTP), is a 466 amino acid protein that contains 3 LRR repeats and plays a role in spermatogenesis. The gene encoding LRRC6 maps to chromosome 8, which encodes approximately 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Chromosome 8 is also associated with Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.
Expand 1 Items
Anti-ADRBK2 Rabbit Polyclonal Antibody
Supplier: Prosci
Anti-ADRBK2 Rabbit Polyclonal Antibody
Expand 1 Items
Anti-SET Rabbit Polyclonal Antibody
Supplier: Prosci
Anti-SET Rabbit Polyclonal Antibody
Expand 1 Items
Anti-CAMK1G Rabbit Polyclonal Antibody
Supplier: Genetex
Rabbit Polyclonal antibody to CaMKI gamma (calcium/calmodulin-dependent protein kinase IG)
Expand 1 Items
Anti-STK38 Mouse Monoclonal Antibody [clone: 2F6]
Supplier: Novus Biologicals
The STK38 Antibody (2F6) from Novus Biologicals is a mouse monoclonal antibody to STK38. This antibody reacts with human. The STK38 Antibody (2F6) has been validated for the following applications: Western Blot, ELISA, Immunohistochemistry, Immunocytochemistry / Immunofluorescence, Immunohistochemistry-Paraffin.
Expand 1 Items
Anti-NUP98 Rat Monoclonal Antibody [clone: 2H10]
Supplier: Abnova
Rat monoclonal antibody raised against partial recombinant NUP98.
Expand 1 Items
Anti-VAV1 Rabbit Polyclonal Antibody
Supplier: Prosci
For WB starting dilution is: 1:1000
Expand 1 Items
Anti-IFNG Mouse Monoclonal Antibody [clone: IFNG/466]
Supplier: Prosci
Recognizes a protein of 20-25kDa, identified as human interferon. This mAb is specific to human IFNg and recognizes both recombinant and native human IFNg. T lymphocytes and NK cells mainly produce IFNg. It is a pleiotropic cytokine involved in the regulation of nearly all phases of immune and inflammatory responses, including the activation, growth and differentiation of T cell, B cells, macrophages, NK cells and other cell types such as endothelial cells and fibroblasts. It has weak anti-viral and anti-proliferative activity, and potentiates the antiviral and anti-tumor effects of IFNa/b (type I interferon).
Expand 1 Items
Anti-CTDSPL2 Rabbit Polyclonal Antibody (Cy7®)
Supplier: Bioss
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
Expand 1 Items
Anti-CTDSPL2 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
Expand 1 Items
Hydromorphone 0.1 mg/ml in Methanol, LoGiCal, LGC Standards
Supplier: LGC Standards
Hydromorphone 0.1 mg/ml in Methanol, LoGiCal, LGC Standards
Expand 1 Items
Anti-CTDSPL2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Supplier: Bioss
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
Expand 1 Items
Anti-PROM2 Rabbit Polyclonal Antibody
Supplier: Prosci
For WB starting dilution is: 1:1000
Expand 1 Items
Anti-PPP3CA Rabbit Polyclonal Antibody
Supplier: Prosci
For WB starting dilution is: 1:1000
Expand 1 Items
Anti-HDAC1 Rabbit Polyclonal Antibody
Supplier: Genetex
Rabbit polyclonal to HDAC1 - ChIP Grade
Expand 1 Items
Anti-MAG Rabbit Polyclonal Antibody
Supplier: Prosci
For WB starting dilution is: 1:1000 For FACS starting dilution is: 1:10~50
Expand 1 Items
Anti-LRRC6 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Supplier: Bioss
The leucine-rich repeat-containing protein 6 (LRRC6), also designated Leucine-rich testis-specific protein (LRTP), is a 466 amino acid protein that contains 3 LRR repeats and plays a role in spermatogenesis. The gene encoding LRRC6 maps to chromosome 8, which encodes approximately 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Chromosome 8 is also associated with Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.
Expand 1 Items
Rat Recombinant IFNGR/IFNGR1 Protein (Fc Tag) (from HEK293 Cells)
Supplier: Sino Biological
A DNA sequence encoding the rat IFNGR (Q6P6T3) (Met1-Ser241) was expressed with the Fc region of human IgG1 at the C-terminus.
Expand 1 Items
Anti-LRRC6 Rabbit Polyclonal Antibody (Cy3®)
Supplier: Bioss
The leucine-rich repeat-containing protein 6 (LRRC6), also designated Leucine-rich testis-specific protein (LRTP), is a 466 amino acid protein that contains 3 LRR repeats and plays a role in spermatogenesis. The gene encoding LRRC6 maps to chromosome 8, which encodes approximately 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Chromosome 8 is also associated with Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.
Expand 1 Items
Anti-LRRC6 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
The leucine-rich repeat-containing protein 6 (LRRC6), also designated Leucine-rich testis-specific protein (LRTP), is a 466 amino acid protein that contains 3 LRR repeats and plays a role in spermatogenesis. The gene encoding LRRC6 maps to chromosome 8, which encodes approximately 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Chromosome 8 is also associated with Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.
Expand 1 Items
Anti-CTDSPL2 Rabbit Polyclonal Antibody (Cy5®)
Supplier: Bioss
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
Expand 1 Items
Anti-CTDSPL2 Rabbit Polyclonal Antibody (Cy5.5®)
Supplier: Bioss
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
Expand 1 Items
Anti-CTDSPL2 Rabbit Polyclonal Antibody (Cy3®)
Supplier: Bioss
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
Expand 1 Items
Mouse Recombinant CXADR Protein (His & Fc Tag) (from HEK293 Cells)
Supplier: Sino Biological
A DNA sequence encoding the mouse CXADR (NP_001020363.1) extracellular domain (Met 1-Gly 237) was fused with the C-terminal polyhistidine-tagged Fc region of human IgG1 at the C-terminus.
Expand 1 Items
Human Recombinant LRRTM4 Protein (His Tag) (from HEK293 Cells)
Supplier: Sino Biological
A DNA sequence encoding the human LRRTM4 extracellular domain (NP_001128217.1) (Met 1-Lys 424) was expressed, fused with a polyhistidine tag at the C-terminus.