Protein Molecular Weight Markers
ABclonal Technology CARD14 Rabbit pAb
This gene encodes a caspase recruitment domain-containing protein that is a member of the membrane-associated guanylate kinase (MAGUK) family of proteins. Members of this protein family are scaffold proteins that are involved in a diverse array of cellular processes including cellular adhesion, signal transduction and cell polarity control. This protein has been shown to specifically interact with BCL10, a protein known to function as a positive regulator of cell apoptosis and NF-kappaB activation. Alternate splicing results in multiple transcript variants.
ABclonal Technology CtBP1 Rabbit pAb
This gene encodes a protein that binds to the C-terminus of adenovirus E1A proteins. This phosphoprotein is a transcriptional repressor and may play a role during cellular proliferation. This protein and the product of a second closely related gene, CTBP2, can dimerize. Both proteins can also interact with a polycomb group protein complex which participates in regulation of gene expression during development. Alternative splicing of transcripts from this gene results in multiple transcript variants.
ABclonal Technology ADARB1 Rabbit pAb
This gene encodes the enzyme responsible for pre-mRNA editing of the glutamate receptor subunit B by site-specific deamination of adenosines. Studies in rat found that this enzyme acted on its own pre-mRNA molecules to convert an AA dinucleotide to an AI dinucleotide which resulted in a new splice site. Alternative splicing of this gene results in several transcript variants, some of which have been characterized by the presence or absence of an ALU cassette insert and a short or long C-terminal region.
![ABclonal Technology [KO Validated] CRMP2/DPYSL2 Rabbit pAb](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000107815.jpg-250.jpg)
ABclonal Technology [KO Validated] CRMP2/DPYSL2 Rabbit pAb
This gene encodes a member of the collapsin response mediator protein family. Collapsin response mediator proteins form homo- and hetero-tetramers and facilitate neuron guidance, growth and polarity. The encoded protein promotes microtubule assembly and is required for Sema3A-mediated growth cone collapse, and also plays a role in synaptic signaling through interactions with calcium channels. This gene has been implicated in multiple neurological disorders, and hyperphosphorylation of the encoded protein may play a key role in the development of Alzheimers disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
ABclonal Technology F10 Rabbit pAb
This gene encodes vitamin K-dependent coagulation factor X, a key player in the blood coagulation cascade. Factor X is processed into a mature two-chain form, with the light chain containing two EGF-like domains and the heavy chain holding the catalytic domain. It is activated by factor IXa (intrinsic pathway) or factor VIIa (extrinsic pathway) and then converts prothrombin to thrombin during clotting, in the presence of factor Va, Ca+2, and phospholipids. Mutations in this gene cause factor X deficiency, leading to hemorrhagic conditions. Alternative splicing produces multiple transcript variants that may undergo similar processing to generate mature polypeptides.
ABclonal Technology FUNDC1 Rabbit pAb
This gene encodes a protein with a FUN14 superfamily domain. The function of the encoded protein is not known.
ABclonal Technology INCENP Rabbit pAb
In mammalian cells, centromere-interacting proteins are classified into two groups: constitutive and passenger proteins. Constitutive proteins, which bind centromere proteins, include CENPA, CENPB, CENPC1, and CENPD. Passenger proteins localize to the centromere during specific cell cycle stages and include CENPE, MCAK, KID, cytoplasmic dynein, CliPs, and CENPF/mitosin. Inner centromere proteins (INCENPs), early members of the passenger protein group, are broadly distributed along chromosomes in early mitosis but concentrate at centromeres during mid-metaphase. By telophase, they localize to the midbody in the intercellular bridge and are discarded after cytokinesis.
ABclonal Technology SEC24D Rabbit pAb
The protein encoded by this gene is a member of the SEC24 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec24p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. This gene product is implicated in the shaping of the vesicle, and also in cargo selection and concentration. Mutations in this gene have been associated with Cole-Carpenter syndrome, a disorder affecting bone formation, resulting in craniofacial malformations and bones that break easily. Alternative splicing results in multiple transcript variants encoding different isoforms.
ABclonal Technology CFAP53 Rabbit pAb
This gene belongs to the CFAP53 family. It was found to be differentially expressed by the ciliated cells of frog epidermis and in skin fibroblasts from human. Mutations in this gene are associated with visceral heterotaxy-6, which implicates this gene in determination of left-right asymmetric patterning.
ABclonal Technology DIAPH2 Rabbit pAb
The product of this gene belongs to the diaphanous subfamily of the formin homology family of proteins. This gene may play a role in the development and normal function of the ovaries. Defects in this gene have been linked to premature ovarian failure 2. Alternatively spliced transcript variants encoding different isoforms have been identified.
ABclonal Technology RTN4RL1 Rabbit pAb
Enables signaling receptor activity. Predicted to be involved in negative regulation of axon regeneration. Located in cell surface. Is anchored component of plasma membrane.
ABclonal Technology RAIDD/CRADD Rabbit mAb
This gene encodes a protein containing a death domain (DD) motif. This protein recruits caspase 2/ICH1 to the cell death signal transduction complex, which includes tumor necrosis factor receptor 1 (TNFR1A) and RIPK1/RIP kinase, and acts in promoting apoptosis. A mutation in this gene was associated with cognitive disability. A related pseudogene is found on chromosome 3. Alternative splicing results in multiple transcript variants.
ABclonal Technology APOBEC3G Rabbit pAb
This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. The protein encoded by this gene catalyzes site-specific deamination of both RNA and single-stranded DNA. The encoded protein has been found to be a specific inhibitor of human immunodeficiency virus-1 (HIV-1) infectivity.
ABclonal Technology PPA2 Rabbit pAb
The protein encoded by this gene is localized to the mitochondrion, is highly similar to members of the inorganic pyrophosphatase (PPase) family, and contains the signature sequence essential for the catalytic activity of PPase. PPases catalyze the hydrolysis of pyrophosphate to inorganic phosphate, which is important for the phosphate metabolism of cells. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
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.