4577 Results for: "Endotoxinov\\\\\\\\u00E9+Testy"

Supplier: Abcam

Recombinant Human MAGEA5 protein is a Human Full Length protein, in the 1 to 124 aa range, expressed in Escherichia coli, with >85% purity and suitable for SDS-PAGE, MS.

Supplier: Abcam

Recombinant Human ASIC3 protein is a Human Fragment protein, in the 83 to 301 aa range, expressed in Escherichia coli, with >90% purity and suitable for SDS-PAGE.

Supplier: Abcam

Recombinant human TFIIS protein is a Human Full Length protein, in the 1 to 299 aa range, expressed in Escherichia coli, with >85% purity and suitable for SDS-PAGE, MS.

Supplier: Abcam

Recombinant Human PDILT protein is a Human Full Length protein, in the 21 to 584 aa range, expressed in HEK 293, with >95% purity, <1 EU/µg endotoxin level and suitable for SDS-PAGE, HPLC.

Supplier: Antibodies.com

Mouse monoclonal [HH1/957] antibody to Histone H1 for flow cytometry, IF, WB and IHC-P with samples derived from human, mouse and rat.

Supplier: Antibodies.com

Mouse monoclonal [MEM-M6/2] antibody to CD147 for Flow Cytometry and IHC-P with samples derived from Human and Porcine.

Supplier: Abcam

Recombinant Human IGSF11 protein (Tagged) is a Human Fragment protein, in the 24 to 241 aa range, expressed in Escherichia coli, with >90% purity and suitable for SDS-PAGE.

Supplier: Abcam

Recombinant human PBK/SPK protein is a Human Full Length protein, expressed in Baculovirus infected Sf9, with >90% purity and suitable for WB, FuncS.

Supplier: Abcam

Recombinant Human SPACA3 protein is a Human Full Length protein, in the 1 to 215 aa range, expressed in Wheat germ and suitable for ELISA, WB.

Supplier: Abcam

Recombinant Human KK-LC-1 VLP protein (His tag) is a Human Full Length protein, in the 1 to 113 aa range, expressed in Mammalian, <1 EU/µg endotoxin level and suitable for SDS-PAGE.

Supplier: Abcam

Recombinant Human XAGE1 protein is a Human Full Length protein, in the 1 to 81 aa range, expressed in Escherichia coli, with >85% purity and suitable for SDS-PAGE, MS.

Supplier: Abcam

Recombinant human PBK/SPK protein is a Human Full Length protein, expressed in Baculovirus infected Sf9, with >90% purity and suitable for SDS-PAGE.

Supplier: Abcam

Recombinant Human Semenogelin I protein is a Human Fragment protein, in the 24 to 402 aa range, expressed in HEK 293, with >95% purity, <0,1 EU/µg endotoxin level and suitable for SDS-PAGE, HPLC.

Supplier: Antibodies.com

Recombinant rabbit monoclonal [HH1/1784R] antibody to Histone H1 for WB, flow cytometry, IF and IHC-P with samples derived from human, mouse and rat.

Supplier: Antibodies.com

Mouse monoclonal [MEM-M6/1] antibody to CD147 for Flow Cytometry, IP, WB and IHC-P with samples derived from Human.

Supplier: Bioss

TSKS is a 592 amino acid protein that is highly expressed in human testicular tissue. Low levels of TSKS are detectable in prostate, placenta, fetal liver, thymus, and mammary gland tissues. TSKS is found to be downregulated in cancerous testicular tissue from seminoma, teratocarcinoma, embryonal and Leydig cell tumors concurrently with high expression in neighboring premalignant carcinoma. TSKS protein contains an N-terminal signal peptide, but does not contain a transmembrane region. TSKS has many potential phosphorylation and glycosylation sites and is phosphorylated by soluble recombinant TSSK2 in vitro. It is thought that TSKS likely plays a physiological role in spermatogenesis or spermiogenesis.

Supplier: Abcam

Recombinant human KDM5B / PLU1 / Jarid1B protein is a Human Fragment protein, in the 2 to 751 aa range, expressed in Baculovirus infected Sf9, with ≥90% purity and suitable for SDS-PAGE, FuncS.

Supplier: Bioss

TSKS is a 592 amino acid protein that is highly expressed in human testicular tissue. Low levels of TSKS are detectable in prostate, placenta, fetal liver, thymus, and mammary gland tissues. TSKS is found to be downregulated in cancerous testicular tissue from seminoma, teratocarcinoma, embryonal and Leydig cell tumors concurrently with high expression in neighboring premalignant carcinoma. TSKS protein contains an N-terminal signal peptide, but does not contain a transmembrane region. TSKS has many potential phosphorylation and glycosylation sites and is phosphorylated by soluble recombinant TSSK2 in vitro. It is thought that TSKS likely plays a physiological role in spermatogenesis or spermiogenesis.

Supplier: Bioss

TSKS is a 592 amino acid protein that is highly expressed in human testicular tissue. Low levels of TSKS are detectable in prostate, placenta, fetal liver, thymus, and mammary gland tissues. TSKS is found to be downregulated in cancerous testicular tissue from seminoma, teratocarcinoma, embryonal and Leydig cell tumors concurrently with high expression in neighboring premalignant carcinoma. TSKS protein contains an N-terminal signal peptide, but does not contain a transmembrane region. TSKS has many potential phosphorylation and glycosylation sites and is phosphorylated by soluble recombinant TSSK2 in vitro. It is thought that TSKS likely plays a physiological role in spermatogenesis or spermiogenesis.

Supplier: Abcam

Recombinant Human PBK/SPK protein is a Human Full Length protein, in the 1 to 322 aa range, expressed in Escherichia coli, with >95% purity and suitable for SDS-PAGE, MS.

Supplier: Bioss

TSKS is a 592 amino acid protein that is highly expressed in human testicular tissue. Low levels of TSKS are detectable in prostate, placenta, fetal liver, thymus, and mammary gland tissues. TSKS is found to be downregulated in cancerous testicular tissue from seminoma, teratocarcinoma, embryonal and Leydig cell tumors concurrently with high expression in neighboring premalignant carcinoma. TSKS protein contains an N-terminal signal peptide, but does not contain a transmembrane region. TSKS has many potential phosphorylation and glycosylation sites and is phosphorylated by soluble recombinant TSSK2 in vitro. It is thought that TSKS likely plays a physiological role in spermatogenesis or spermiogenesis.

Supplier: Bioss

TSKS is a 592 amino acid protein that is highly expressed in human testicular tissue. Low levels of TSKS are detectable in prostate, placenta, fetal liver, thymus, and mammary gland tissues. TSKS is found to be downregulated in cancerous testicular tissue from seminoma, teratocarcinoma, embryonal and Leydig cell tumors concurrently with high expression in neighboring premalignant carcinoma. TSKS protein contains an N-terminal signal peptide, but does not contain a transmembrane region. TSKS has many potential phosphorylation and glycosylation sites and is phosphorylated by soluble recombinant TSSK2 in vitro. It is thought that TSKS likely plays a physiological role in spermatogenesis or spermiogenesis.

Supplier: Bioss

TSKS is a 592 amino acid protein that is highly expressed in human testicular tissue. Low levels of TSKS are detectable in prostate, placenta, fetal liver, thymus, and mammary gland tissues. TSKS is found to be downregulated in cancerous testicular tissue from seminoma, teratocarcinoma, embryonal and Leydig cell tumors concurrently with high expression in neighboring premalignant carcinoma. TSKS protein contains an N-terminal signal peptide, but does not contain a transmembrane region. TSKS has many potential phosphorylation and glycosylation sites and is phosphorylated by soluble recombinant TSSK2 in vitro. It is thought that TSKS likely plays a physiological role in spermatogenesis or spermiogenesis.

Supplier: Bioss

TSKS is a 592 amino acid protein that is highly expressed in human testicular tissue. Low levels of TSKS are detectable in prostate, placenta, fetal liver, thymus, and mammary gland tissues. TSKS is found to be downregulated in cancerous testicular tissue from seminoma, teratocarcinoma, embryonal and Leydig cell tumors concurrently with high expression in neighboring premalignant carcinoma. TSKS protein contains an N-terminal signal peptide, but does not contain a transmembrane region. TSKS has many potential phosphorylation and glycosylation sites and is phosphorylated by soluble recombinant TSSK2 in vitro. It is thought that TSKS likely plays a physiological role in spermatogenesis or spermiogenesis.

Supplier: Bioss

TSKS is a 592 amino acid protein that is highly expressed in human testicular tissue. Low levels of TSKS are detectable in prostate, placenta, fetal liver, thymus, and mammary gland tissues. TSKS is found to be downregulated in cancerous testicular tissue from seminoma, teratocarcinoma, embryonal and Leydig cell tumors concurrently with high expression in neighboring premalignant carcinoma. TSKS protein contains an N-terminal signal peptide, but does not contain a transmembrane region. TSKS has many potential phosphorylation and glycosylation sites and is phosphorylated by soluble recombinant TSSK2 in vitro. It is thought that TSKS likely plays a physiological role in spermatogenesis or spermiogenesis.

Supplier: Bioss

TSKS is a 592 amino acid protein that is highly expressed in human testicular tissue. Low levels of TSKS are detectable in prostate, placenta, fetal liver, thymus, and mammary gland tissues. TSKS is found to be downregulated in cancerous testicular tissue from seminoma, teratocarcinoma, embryonal and Leydig cell tumors concurrently with high expression in neighboring premalignant carcinoma. TSKS protein contains an N-terminal signal peptide, but does not contain a transmembrane region. TSKS has many potential phosphorylation and glycosylation sites and is phosphorylated by soluble recombinant TSSK2 in vitro. It is thought that TSKS likely plays a physiological role in spermatogenesis or spermiogenesis.

Supplier: Abcam

Recombinant Human IL-13 receptor alpha 1 protein is a Human Fragment protein, in the 22 to 343 aa range, expressed in HEK 293, with >98% purity, <1 EU/µg endotoxin level and suitable for SDS-PAGE, FuncS.

Supplier: Bioss

C5orf48 (chromosome 5 open reading frame 48), also known as FLJ27505, MGC163367 or MGC163369, is a 134 amino acid protein. Encoded by a gene that maps to human chromosome 5q23.2, C5orf48 is linked to Autosomal dominant leukodystrophy (ADLD). Chromosome 5 makes up approximately 6% of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

Supplier: Bioss

Made up of nearly 146 million bases, chromosome 8 encodes about 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. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf42 gene product has been provisionally designated C8orf42 pending further characterization.

Supplier: Bioss

Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf49 gene product has been provisionally designated C1orf49 pending further characterization. There are four isoforms of C1orf49 that are produced as a result of alternative splicing events.