Miscellaneous Catalog

MISCELLANEOUS

RNA ENCODED PROTEIN SPECIES CATALOG NUMBER FROM PRICE
BioCapTM ERAS mRNA GTPase ERas Human 2000101 500 ug $1,705
BioCapTM SERPINA1 mRNA Alpha-1-antitrypsin Human 2000201 500 ug $1,705
BioCapTM SERPINA1 Z Type mutant mRNA Alpha-1-antitrypsin Z Type mutant Human 2000301 500 ug $1,705
BioCapTM ELANE mRNA Neutrophil elastase Human 2000401 500 ug $1,705
BioCapTM CXCL12 Isoform alpha mRNA Stromal cell-derived factor 1 Isoform alpha Human 2000501 500 ug $1,705
BioCapTM CXCL12 Isoform gamma mRNA Stromal cell-derived factor 1 Isoform gamma Human 2000601 500 ug $1,705
BioCapTM OLA1 mRNA Obg-like ATPase 1 Human 2000701 500 ug $1,705
BioCapTM DCT mRNA L-dopachrome tautomerase Human 2000801 500 ug $1,705
BioCapTM Mef2c mRNA Myocyte-specific enhancer factor 2C Mouse 2000901 500 ug $1,705
BioCapTM Tbx5 mRNA T-box transcription factor TBX5 Mouse 2001001 500 ug $1,705
BioCapTM Gata4 mRNA Transcription factor GATA-4 Mouse 2001101 500 ug $1,705
BioCapTM Hand2 mRNA Heart- and neural crest derivatives-expressed protein 2 Mouse 2001201 500 ug $1,705
BioCapTM Pou3f2 mRNA POU domain, class 3, transcription factor 2 Mouse 2001301 500 ug $1,705
BioCapTM pou3f2 mRNA POU domain, class 3, transcription factor 2 Zebrafish 2001401 500 ug $1,705

MISCELLANEOUS

A growing number of genes that are involved in different cellular and molecular processes are included in this category of mRNA mimics. Transcription factors, stromal cell-derived factors, myocyte-specific enhancers, and genes implicated in tissue remodelling are currently included in this list.

BioCapTM ERAS mRNA

https://www.pharna.com/product/2000101/

The protein-coding gene ERAS (ES Cell Expressed Ras) is. Immunodeficiency 54 and Loose Anagen Hair Syndrome are diseases linked to ERAS. Breast cancer pathway and PI3K/Akt Signaling are a couple of the pathways that are connected to it. GTP binding is mentioned in the Gene Ontology (GO) entries for this gene. This gene’s significant paralog is NRAS.

BioCapTM SERPINA1 mRNA

https://www.pharna.com/product/2000201/

The gene SERPINA1 (Serpin Family A Member 1) codes for proteins. Alpha-1-Antitrypsin Deficiency and Hemorrhagic Disease Caused by the Pittsburgh Mutation in Alpha-1-Antitrypsin are two conditions linked to SERPINA1. Its related pathways include Transport to the Golgi and later modification in response to increased platelet cytosolic Ca2+. The gene’s Gene Ontology (GO) entries mention identical protein binding and protease binding. The gene SERPINA4 has a significant paralog.

BioCapTM SERPINA1 Z Type mutant mRNA

https://www.pharna.com/product/2000301/

Elastase is its main target, but it also has a modest affinity for thrombin and plasmin. Trypsin, chymotrypsin, and plasminogen activator are irreversibly inhibited. The aberrant version has proteolytic action against insulin and plasmin and inhibits insulin-induced NO synthesis in platelets. It also shortens the time required for coagulation. 

BioCapTM ELANE mRNA

https://www.pharna.com/product/2000401/

It works by modifying the actions of granulocytes, macrophages, and natural killer cells. blocks chemotaxis and the production of neutrophil enzymes that are C5a dependent.

BioCapTM CXCL12 Isoform alpha mRNA

https://www.pharna.com/product/2000501/

A gene that codes for proteins is called CXCL12 (C-X-C Motif Chemokine Ligand 12). Ischemia and Human Immunodeficiency Virus Type 1 are two conditions linked to CXCL12. Apoptotic Pathways in Synovial Fibroblasts and MIF Mediated Glucocorticoid Regulation are two of its associated pathways. This gene has chemokine function and signalling receptor binding as Gene Ontology (GO) annotations.

BioCapTM CXCL12 Isoform gamma mRNA

https://www.pharna.com/product/2000601/

Activates as a chemoattractant on monocytes and T cells but not neutrophils. increases the amount of intracellular calcium ions and causes chemotaxis by activating the C-X-C chemokine receptor CXCR4. The chemotactic activity of SDF-1-beta(3-72) and SDF-1-alpha(3-67) is decreased.

BioCapTM OLA1 mRNA

https://www.pharna.com/product/2000701/

Obg Like ATPase 1 (OLA1) is a gene that codes for proteins. Hereditary Breast Ovarian Cancer Syndrome is one of the conditions linked to OLA1. Response to elevated platelet cytosolic Ca2+ is one of its associated mechanisms. GTP binding and ribosome binding are two Gene Ontology (GO) categories associated with this gene.

BioCapTM DCT mRNA

https://www.pharna.com/product/2000801/

Dopachrome Tautomerase is a gene that codes for proteins. Type III and Albinism, as well as Oculocutaneous Albinism, are diseases connected to DCT. Metabolism and the control of SLIT and ROBO expression are two of its linked pathways. Oxidoreductase activity and dopachrome isomerase activity are GO tags associated with this gene.

BioCapTM Mef2c mRNA

https://www.pharna.com/product/2000901/

Myocyte Enhancer Factor 2C (MEF2C) is a gene that codes for proteins. Neurodevelopmental Disorder With Hypotonia, Stereotypic Hand Movements, Impaired Language, and Autism Spectrum Disorder are diseases connected to MEF2C. The MyD88-dependent cascade started on the endosome and gene expression are two of its related mechanisms. (Transcription). DNA-binding transcription factor activity and protein heterodimerization activity are GO classifications for this gene.

BioCapTM Tbx5 mRNA

https://www.pharna.com/product/2001001/

T-Box Transcription Factor 5 (TBX5) is a gene that codes for proteins. TBX5 has been linked to Holt-Oram Syndrome and Patent Foramen Ovale. Gene expression (transcription) and cardiac conduction are two of its linked processes. Transcription factor binding and DNA-binding transcription factor activity are two Gene Ontology (GO) categories associated with this gene. TBX4 is a significant paralog of this gene.

BioCapTM Gata4 mRNA

https://www.pharna.com/product/2001101/

A gene for protein coding is called GATA4 (GATA Binding Protein 4). Testicular Anomalies With Or Without Congenital Heart Disease and Atrial Septal Defect 2 are two conditions linked to GATA4. Gene expression (transcription) and cardiac conduction are two of its linked processes. This gene has chromatin binding and DNA-binding transcription factor function as Gene Ontology (GO) annotations.

BioCapTM Hand2 mRNA

https://www.pharna.com/product/2001201/

A gene called HAND2 (Heart and Neural Crest Derivatives Expressed 2) codes for proteins. Cardiomyopathy, Dilated, 1A and Cardiomyopathy, Dilated, 1H are conditions linked to HAND2. Gene expression (transcription), NFAT, and cardiac hypertrophy are some of the mechanisms connected to it. Protein homodimerization activity and protein heterodimerization activity are both GO classifications for this gene.

BioCapTM Pou3f2 mRNA

https://www.pharna.com/product/2001301/

The gene POU3F2 (POU Class 3 Homeobox 2) codes for proteins. POU3F2 is linked to the diseases microphthalmia and melanoma. Development of the nervous system and the beginning of Schwann cell myelination, which is regulated by EGR2 and SOX10, are two of its related pathways. DNA-binding transcription factor activity and identical protein binding are two Gene Ontology (GO) categories that are connected to this gene.

BioCapTM pou3f2 mRNA

https://www.pharna.com/product/2001401/

In the process of patterning the embryonic brain, transcription factors may play an important role in shaping its shape during the embryonic development.