Protein Molecular Weight Markers
Proteintech Group Inc Broad range prestained protein marker
The PL00002 Broad Range Protein Marker is a ready-to-use three-color proteinstandard with 13 prestained proteins covering a wide range of molecular weightsfrom 3 to 245 kDa in Tris-Glycine buffer. The PL00002 Broad Range Prestained ProteinMarker is designed for monitoring protein separation during SDS-polyacrylamide gelelectrophoresis, verification of Western transfer efficiency on membranes(nitrocellulose, PVDF, or nylon) and for estimating the size of proteins.
ABclonal Technology MIIP Rabbit pAb
This gene encodes a protein that interacts with the oncogene protein insulin-like growth factor binding protein 2 and may function as an inhibitor of cell migration and invasion. This protein also interacts with the cell division protein 20 and may be involved in regulating mitotic progression. This protein may function as a tumor suppressor by inhibiting the growth or certain cancers.
ABclonal Technology HOOK2 Rabbit mAb
Hook proteins are cytosolic coiled-coil proteins that contain conserved N-terminal domains, which attach to microtubules, and more divergent C-terminal domains, which mediate binding to organelles. The Drosophila Hook protein is a component of the endocytic compartment.
Cell Signaling Technology Biotinylated Protein Ladder Detection Pack 650 µl
Biotinylated Protein Ladder Detection Pack 650 µl
ABclonal Technology STX6 Rabbit pAb
Enables syntaxin binding activity. Involved in several processes, including Golgi ribbon formation, retrograde transport, endosome to Golgi, and vesicle fusion. Acts upstream of or within endocytic recycling. Located in several cellular components, including early endosome, perinuclear region of cytoplasm, and trans-Golgi network. Part of SNARE complex.
ABclonal Technology USP9X Rabbit pAb
This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
ABclonal Technology NTPCR Rabbit pAb
The protein encoded by this gene is a non-specific nucleoside triphosphatase that is slow-acting in vitro. This gene is overexpressed in many tumor tissues, and while it is not essential for the cell, overexpression is cytotoxic. However, the cytotoxicity is not related to its triphosphatase activity.
ABclonal Technology REXO2 Rabbit pAb
This gene encodes a 3-to-5 exonuclease specific for small (primarily 5 nucleotides or less in length) single-stranded RNA and DNA oligomers. This protein may have a role in DNA repair, replication, and recombination, and in RNA processing and degradation. It may also be involved in resistance of human cells to UV-C-induced cell death through its role in the DNA repair process.
ABclonal Technology RRAGA Rabbit pAb
Enables several functions, including GTP binding activity, protein dimerization activity, and ubiquitin protein ligase binding activity. Involved in several processes, including cellular response to amino acid starvation, negative regulation of autophagy, and positive regulation of TORC1 signaling. Located in lysosome and nucleus. Colocalizes with GATOR1 complex.
ABclonal Technology ACOT2 Rabbit pAb
This gene encodes a member of the acyl-CoA thioesterase protein family, and is one of four acyl-CoA hydrolase genes located in a cluster on chromosome 14. Alternative splicing results in multiple transcript variants.
ABclonal Technology PLD4 Rabbit pAb
Predicted to enable single-stranded DNA 5-3 exodeoxyribonuclease activity. Predicted to be involved in hematopoietic progenitor cell differentiation, phagocytosis, and regulation of cytokine production involved in inflammatory response. Predicted to be located in early endosome and endoplasmic reticulum membrane. Predicted to be active in several cellular components, including endoplasmic reticulum, phagocytic vesicle, and trans-Golgi network membrane.
ABclonal Technology StAR Rabbit pAb
The protein encoded by this gene plays a key role in the acute regulation of steroid hormone synthesis by enhancing the conversion of cholesterol into pregnenolone. This protein permits the cleavage of cholesterol into pregnenolone by mediating the transport of cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane. Mutations in this gene are a cause of congenital lipoid adrenal hyperplasia (CLAH), also called lipoid CAH. A pseudogene of this gene is located on chromosome 13.
ABclonal Technology ITGAX Rabbit pAb
This gene encodes the integrin alpha X chain protein. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This protein combines with the beta 2 chain (ITGB2) to form a leukocyte-specific integrin referred to as inactivated-C3b (iC3b) receptor 4 (CR4). The alpha X beta 2 complex seems to overlap the properties of the alpha M beta 2 integrin in the adherence of neutrophils and monocytes to stimulated endothelium cells, and in the phagocytosis of complement coated particles. Two transcript variants encoding different isoforms have been found for this gene.
ABclonal Technology PPA1 Rabbit pAb
The protein encoded by this gene is a member of the inorganic pyrophosphatase (PPase) family. PPases catalyze the hydrolysis of pyrophosphate to inorganic phosphate, which is important for the phosphate metabolism of cells. Studies of a similar protein in bovine suggested a cytoplasmic localization of this enzyme.
ABclonal Technology DDX3Y Rabbit pAb
The protein encoded by this gene is a member of the DEAD-box RNA helicase family, characterized by nine conserved motifs, included the conserved Asp-Glu-Ala-Asp (DEAD) motif. These motifs are thought to be involved in ATP binding, hydrolysis, RNA binding, and in the formation of intramolecular interactions. This protein shares high similarity to DDX3X, on the X chromosome, but a deletion of this gene is not complemented by DDX3X. Mutations in this gene result in male infertility, a reduction in germ cell numbers, and can result in Sertoli-cell only sydrome. Pseudogenes sharing similarity to both this gene and the DDX3X paralog are found on chromosome 4 and the X chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms.