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220 results for "44686"

220 Results for: "44686"

Corrected to: 4,6,6

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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.

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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

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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.

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Anti-VIM Mouse Monoclonal Antibody [clone: 4F2E9]

Anti-VIM Mouse Monoclonal Antibody [clone: 4F2E9]

Supplier: Abnova

Mouse monoclonal antibody raised against partial recombinant VIM.

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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.

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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.

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Anti-ADRBK2 Rabbit Polyclonal Antibody

Supplier: Prosci

Anti-ADRBK2 Rabbit Polyclonal Antibody

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Anti-SET Rabbit Polyclonal Antibody

Supplier: Prosci

Anti-SET Rabbit Polyclonal Antibody

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Anti-CAMK1G Rabbit Polyclonal Antibody

Supplier: Genetex

Rabbit Polyclonal antibody to CaMKI gamma (calcium/calmodulin-dependent protein kinase IG)

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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.

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Anti-NUP98 Rat Monoclonal Antibody [clone: 2H10]

Anti-NUP98 Rat Monoclonal Antibody [clone: 2H10]

Supplier: Abnova

Rat monoclonal antibody raised against partial recombinant NUP98.

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Anti-VAV1 Rabbit Polyclonal Antibody

Anti-VAV1 Rabbit Polyclonal Antibody

Supplier: Prosci

For WB starting dilution is: 1:1000

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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).

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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.

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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.

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Hydromorphone 0.1 mg/ml in Methanol, LoGiCal, LGC Standards

Hydromorphone 0.1 mg/ml in Methanol, LoGiCal, LGC Standards

Supplier: LGC Standards

Hydromorphone 0.1 mg/ml in Methanol, LoGiCal, LGC Standards

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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.

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Anti-PROM2 Rabbit Polyclonal Antibody

Anti-PROM2 Rabbit Polyclonal Antibody

Supplier: Prosci

For WB starting dilution is: 1:1000

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Anti-PPP3CA Rabbit Polyclonal Antibody

Anti-PPP3CA Rabbit Polyclonal Antibody

Supplier: Prosci

For WB starting dilution is: 1:1000

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Anti-HDAC1 Rabbit Polyclonal Antibody

Supplier: Genetex

Rabbit polyclonal to HDAC1 - ChIP Grade

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Anti-MAG Rabbit Polyclonal Antibody

Anti-MAG Rabbit Polyclonal Antibody

Supplier: Prosci

For WB starting dilution is: 1:1000 For FACS starting dilution is: 1:10~50

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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.

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Rat Recombinant IFNGR/IFNGR1 Protein (Fc Tag) (from HEK293 Cells)

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.

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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.

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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.

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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.

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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.

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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.

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Mouse Recombinant CXADR  Protein (His & Fc Tag) (from HEK293 Cells)

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.

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Human Recombinant LRRTM4 Protein (His Tag) (from HEK293 Cells)

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.

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