Protein Molecular Weight Markers
Biotium Primary Antibody Rabbit IgG Fc N2507.RFC CF594 1/EA
Alpaca Anti-Rabbit IgG (Fc) rVHH (N2507 RFC) is a recombinant Alpaca VHH antibody that recognizes the Fc fragment of rabbit IgG and is validated for immunofluorescence Red fluorescent photostable CF594 dye has Ex/Em at 593/614 nm Unit size 500 uL at 0 1 mg/mL
ABclonal Technology PAPD7 Rabbit pAb
The protein encoded by this gene is a DNA polymerase that is likely involved in DNA repair. In addition, the encoded protein may be required for sister chromatid adhesion. Alternatively spliced transcript variants that encode different isoforms have been described.
ABclonal Technology MELK Rabbit pAb
Enables calcium ion binding activity, non-membrane spanning protein tyrosine kinase activity, and protein serine/threonine kinase activity. Involved in apoptotic process, cell population proliferation, and protein autophosphorylation. Located in cell cortex and plasma membrane.
ABclonal Technology SRSF7 Rabbit pAb
The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an N-terminal RNA recognition motif (RRM) for binding RNA and a C-terminal RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Multiple transcript variants encoding different isoforms have been found for this gene.
ABclonal Technology GIPC1 Rabbit pAb
GIPC1 is a scaffolding protein that regulates cell surface receptor expression and trafficking (Lee et al., 2008 [PubMed 18775991]).
ABclonal Technology GSTA1 Rabbit pAb
This gene encodes a member of a family of enzymes that function to add glutathione to target electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins, and products of oxidative stress. This action is an important step in detoxification of these compounds. This subfamily of enzymes has a particular role in protecting cells from reactive oxygen species and the products of peroxidation. Polymorphisms in this gene influence the ability of individuals to metabolize different drugs. This gene is located in a cluster of similar genes and pseudogenes on chromosome 6. Alternative splicing results in multiple transcript variants.
ABclonal Technology ZSCAN4C Rabbit pAb
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Acts upstream of or within negative regulation of mitotic recombination, regulation of transcription by RNA polymerase II, and telomere maintenance via telomere lengthening. Located in chromosome, telomeric region, cytoplasm, and nucleus. Is expressed in 1-cell stage embryo, 2-cell stage embryo, primary oocyte, and secondary oocyte. Orthologous to human ZSCAN4 (zinc finger and SCAN domain containing 4).
ABclonal Technology HTRA2 Rabbit pAb
This gene encodes a serine protease. The protein has been localized in the endoplasmic reticulum and interacts with an alternatively spliced form of mitogen-activated protein kinase 14. The protein has also been localized to the mitochondria with release to the cytosol following apoptotic stimulus. The protein is thought to induce apoptosis by binding the apoptosis inhibitory protein baculoviral IAP repeat-containing 4. Nuclear localization of this protein has also been observed. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms.
ABclonal Technology TXNDC12 Rabbit pAb
This gene encodes a member of the thioredoxin superfamily. Members of this family are characterized by a conserved active motif called the thioredoxin fold that catalyzes disulfide bond formation and isomerization. This protein localizes to the endoplasmic reticulum and has a single atypical active motif. The encoded protein is mainly involved in catalyzing native disulfide bond formation and displays activity similar to protein-disulfide isomerases. This protein may play a role in defense against endoplasmic reticulum stress. Alternate splicing results in both coding and non-coding variants.
ABclonal Technology SERPINI1 Rabbit pAb
This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The protein is primarily secreted by axons in the brain, and preferentially reacts with and inhibits tissue-type plasminogen activator. It is thought to play a role in the regulation of axonal growth and the development of synaptic plasticity. Mutations in this gene result in familial encephalopathy with neuroserpin inclusion bodies (FENIB), which is a dominantly inherited form of familial encephalopathy and epilepsy characterized by the accumulation of mutant neuroserpin polymers. Multiple alternatively spliced variants, encoding the same protein, have been identified.
ABclonal Technology NOTCH2 Rabbit pAb
This gene encodes a member of the Notch family, a group of Type 1 transmembrane proteins with an extracellular domain containing multiple epidermal growth factor-like (EGF) repeats and an intracellular domain with diverse domains. Notch family proteins regulate developmental processes by controlling cell fate decisions through an evolutionarily conserved intercellular signaling pathway. In Drosophila, Notch interacts with ligands (delta, serrate) to regulate development, and similar ligands have been identified in humans, though their interactions with human Notch proteins are not fully understood. This protein is cleaved in the trans-Golgi network and presented as a heterodimer on the cell surface, acting as a receptor for membrane-bound ligands. It may be involved in vascular, renal, and hepatic development. Two transcript variants encoding different isoforms have been identified.
ABclonal Technology TCTA Rabbit pAb
Involved in negative regulation of osteoclast differentiation and osteoclast fusion. Predicted to be integral component of membrane.
ABclonal Technology GALK1 Rabbit pAb
Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts during infancy and presenile cataracts in the adult population.
ABclonal Technology SNW1 Rabbit pAb
This gene, a member of the SNW gene family, encodes a coactivator that enhances transcription from some Pol II promoters. This coactivator can bind to the ligand-binding domain of the vitamin D receptor and to retinoid receptors to enhance vitamin D-, retinoic acid-, estrogen-, and glucocorticoid-mediated gene expression. It can also function as a splicing factor by interacting with poly(A)-binding protein 2 to directly control the expression of muscle-specific genes at the transcriptional level. Finally, the protein may be involved in oncogenesis since it interacts with a region of SKI oncoproteins that is required for transforming activity. Alternative splicing results in multiple transcript variants.
ABclonal Technology Ran Rabbit pAb
RAN (ras-related nuclear protein) is a small GTP-binding protein in the RAS superfamily, essential for RNA and protein translocation through the nuclear pore complex. It also regulates DNA synthesis and cell cycle progression. RANs nuclear localization requires regulator of chromosome condensation 1 (RCC1). Mutations in RAN disrupt DNA synthesis. Besides its role in nuclear-cytosol exchange, RAN also influences microtubule network formation and organization, particularly during mitosis. RCC1 generates a high concentration of RAN-GTP near chromatin, promoting microtubule nucleation. RAN is an androgen receptor (AR) coactivator and interacts differently with polyglutamine in AR. Expansion of polyglutamine repeats in AR is linked to Kennedys disease (spinal and bulbar muscular atrophy), where weak coactivation may lead to partial androgen insensitivity.