Protein Molecular Weight Markers
S2 Media 15x100mm Chameleon™ COLOREX™ B. cereus, 10/pack
Chameleon™ COLOREX™ B. cereus s a selective and differential, chromogenic culture medium used for the qualitative direct detection and enumeration of Bacillus cereus in environmental and food samples. Bacillus cereus is a spore-forming bacterium, which produces toxins, that is frequently isolated from soil and foods. These toxins result in two types of illness: one is characterized by diarrhea (long incubation of 8-16 hours) and the other by nausea and vomiting (short incubation of 1-6 hours). Further identification testing should be performed on suspect colonies.• Product meets CLSI performance criteria.• Chameleon™ COLOREX™ B. cereus should be used by trained professionals within a laboratory setting. • Product is not intended for use in the diagnosis or treatment of disease or other human conditions.
S2 Media 15x100mm Chameleon™ COLOREX™ Candida Plus, 10/pack
Chameleon™ COLOREX™ Candida Plus is a selective and differential, chromogenic culture medium used for the qualitative direct detection and presumptive identification of Candida species, including Candida auris. Test specimens include swabs from skin, throat, ears, and vaginal specimens, as well as sputum, urine, and stools. Samples should be tested in parallel to cultures on Sabouraud Dextrose Agar. Further identification, susceptibility testing, and epidemiological typing is needed on suspect colonies.• Product meets CLSI performance criteria.• Chameleon™ COLOREX™ Candida Plus should be used by trained professionals within a laboratory setting. • For in vitro diagnostic (IVD) use.• Product is not intended for use in the diagnosis or treatment of disease or other human conditions.
S2 Media 15x100mm Chameleon™ COLOREX™ Candida, 10/pack
Chameleon™ COLOREX™ Candida is a selective and differential, chromogenic culture medium used for the qualitative direct detection and presumptive identification of Candida species. Test specimens include swabs from skin, throat, ears, and vaginal specimens, as well as sputum, urine, and stools. Samples should be tested in parallel to cultures on Sabouraud Dextrose Agar. Further identification, susceptibility testing, and epidemiological typing is needed on suspect colonies.• Product meets CLSI performance criteria.• Chameleon™ COLOREX™ Candida should be used by trained professionals within a laboratory setting. • For in vitro diagnostic (IVD) use.• Product is not intended for use in the diagnosis or treatment of disease or other human conditions.
ABclonal Technology RPL18 Rabbit pAb
Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L18E family of ribosomal proteins that is a component of the 60S subunit. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
ABclonal Technology CDH4 Rabbit pAb
This gene is a classical cadherin from the cadherin superfamily. The encoded protein is a calcium-dependent cell-cell adhesion glycoprotein comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Based on studies in chicken and mouse, this cadherin is thought to play an important role during brain segmentation and neuronal outgrowth. In addition, a role in kidney and muscle development is indicated. Of particular interest are studies showing stable cis-heterodimers of cadherins 2 and 4 in cotransfected cell lines. Previously thought to interact in an exclusively homophilic manner, this is the first evidence of cadherin heterodimerization. Three transcript variants encoding different isoforms have been found for this gene.
ABclonal Technology SLC6A14 Rabbit pAb
This gene encodes a member of the solute carrier family 6. Members of this family are sodium and chloride dependent neurotransmitter transporters. The encoded protein transports both neutral and cationic amino acids. This protein may also function as a beta-alanine carrier. Mutations in this gene may be associated with X-linked obesity. A pseudogene of this gene is found on chromosome X.
ABclonal Technology RNF114 Rabbit pAb
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein polyubiquitination and ubiquitin-dependent protein catabolic process. Located in cytosol and plasma membrane. Biomarker of male infertility.
ABclonal Technology ACBD5 Rabbit pAb
This gene encodes a member of the acyl-Coenzyme A binding protein family, known to function in the transport and distribution of long chain acyl-Coenzyme A in cells. This gene may play a role in the differentiation of megakaryocytes and formation of platelets. A related protein in yeast is involved in autophagy of peroxisomes. A mutation in this gene has been associated with autosomal dominant thrombocytopenia. Alternative splicing results in multiple transcript variants.
ABclonal Technology GPR143 Rabbit pAb
This gene encodes a protein that binds to heterotrimeric G proteins and is targeted to melanosomes in pigment cells. This protein is thought to be involved in intracellular signal transduction mechanisms. Mutations in this gene cause ocular albinism type 1, also referred to as Nettleship-Falls type ocular albinism, a severe visual disorder. A related pseudogene has been identified on chromosome Y.
ABclonal Technology PPP1R12A Rabbit pAb
Myosin phosphatase target subunit 1 (MBS), also known as the myosin-binding subunit of myosin phosphatase, is a key subunit of myosin phosphatase. It regulates actin-myosin interactions downstream of the Rho GTPase. Rho is involved in myosin light chain (MLC) phosphorylation, which triggers smooth muscle contraction and actin-myosin interaction in nonmuscle cells. The active form of RhoA (GTP.RhoA) specifically interacts with MBS, regulating MLC phosphorylation. Rho-kinase, activated by GTP.RhoA, phosphorylates MBS and inactivates myosin phosphatase. Overexpression of RhoA in NIH 3T3 cells increases MBS and MLC phosphorylation. Thus, Rho inhibits myosin phosphatase via Rho-kinase. Several transcript variants encoding different isoforms have been identified for this gene.
ABclonal Technology SSB Rabbit pAb
The protein encoded by this gene is involved in diverse aspects of RNA metabolism, including binding and protecting poly(U) termini of nascent RNA polymerase III transcripts from exonuclease digestion, processing 5 and 3 ends of pre-tRNA precursors, acting as an RNA chaperone, and binding viral RNAs associated with hepatitis C virus. Autoantibodies reacting with this protein are found in the sera of patients with Sjogren syndrome and systemic lupus erythematosus. Alternative promoter usage results in two different transcript variants which encode the same protein.
ABclonal Technology MCL1 Rabbit pAb
This gene encodes an anti-apoptotic protein, which is a member of the Bcl-2 family. Alternative splicing results in multiple transcript variants. The longest gene product (isoform 1) enhances cell survival by inhibiting apoptosis while the alternatively spliced shorter gene products (isoform 2 and isoform 3) promote apoptosis and are death-inducing.
Sigma Aldrich Fine Chemicals Biosciences Gel Filtration Markers Kit for Protein Molecular Weights 29,000-700,000 Da | 1KT
Gel Filtration Markers Kit for Protein Molecular Weights 29,000-700,000 Da | 1KT
ABclonal Technology ELP2 Rabbit pAb
The protein encoded by this gene is a core subunit of the elongator complex, a histone acetyltransferase complex that associates with RNA polymerase II. In addition to histone acetylation, the encoded protein effects transcriptional elongation and may help remodel chromatin.
ABclonal Technology SLC25A4/ANT1 Rabbit pAb
This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy.