Antibody News

GFAP: Roles in Alzheimer's and Schizophrenia

Thursday, February 14, 2013 - 10:56

Glial fibrillary acidic protein (GFAP) is a class III intermediate filament (IF) protein and is used as a marker to distinguish astrocytes from other glial cells during development. GFP may play a role in maintaining mechanical strength and shape in astrocytes but its exact function still remains mostly uncharacterized.  Mutations in GFAP are well-known to cause Alexander disease (1), but recent studies have shown that GFAP may be a useful marker in spinal astrocytoma.  A variant of GFAP, GFAP-gamma was shown to be upregulated in patients with high grade spinal cord astrocytoma compared to normal tissues (2).

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BrdU: Tracking DNA during Cell Divisions

Wednesday, February 13, 2013 - 13:04

Bromodeoxyuridine (BrdU) variously abbreviated as BrdU, BudR, and BrdUrd, is a synthetic thymidine analog that gets incorporated into the DNA of dividing cells during the S-phase of the cell cycle and has a long history of heavy use in molecular and cytokinetic studies (1). Due to its ability to substitute itself to T base, BrdU has 2 major applications: visualization of genomic DNA degradation during cell death (apoptosis) and monitoring of the level of proliferation and cell division. Here, we will focus on the second application based on the usage of an anti-BrdU antibody.

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Beta Catenin Implications for Signaling

Monday, February 11, 2013 - 17:12

The Wnt/beta Catenin signaling pathway plays a critical role in embryonic development, stem cell self-renewal and regeneration. Alterations in this signaling cascade have been implicated in the pathogenesis of cancer. Notably, chronic activation of Wnt/beta-catenin signaling is found in a variety of human malignancies including melanoma, colorectal and hepatocellular carcinomas (1). In adults, aberrant activation of these same biological processes can induce neoplasia and promote tumour progression.

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HA95: Regulator of Nuclear Envelope Dynamics

Thursday, February 7, 2013 - 23:38

HA95 is a nuclear protein with high homology to the nuclear A-kinase anchoring protein AKAP95, involved in the regulation of nuclear envelope-chromatin interactions. Antibody immunostaining data indicate that HA95 is tightly associated with chromatin and the nuclear matrix/lamina network in interphase, and bound to chromatin at mitosis. Intra-nuclear blocking with anti-HA95 antibodies abolishes nuclear breakdown in a mitotic HeLa cell extracts by inhibiting nuclear membrane breakdown and chromatin condensation (1).

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Controlling the HIF-1 Switch

Wednesday, February 6, 2013 - 15:21

Hypoxia-inducible factor-1 is a major transcription factor composed of two subunits: HIF-1alpha and HIF-1 beta. Under normoxic conditions, HIF-1 alpha is targeted to proteosomal degradation via ubiquitination. On the other hand during hypoxic conditions when oxygen concentration is low, HIF-1 alpha is stabilized and translocates to nucleus, where it dimerises with HIF-1 beta to form functional HIF-1. This altered redox state occurring in the cells experiencing hypoxia in turn indicates gene transcription of several angiogenic factors.

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SCP1 a Potential Cancer Target for Immunotherapy

Monday, February 4, 2013 - 12:05

Synaptonemal Complex Protein 1 (SCP1) is a novel tumor antigen that belongs to the growing family of cancer/testis antigens (CTA). SCP-1 is known to be selectively expressed during the meiotic prophase of spermatocytes and is involved in the pairing of homologous chromosomes during meiosis I. Investigation of a broad spectrum of normal and malignant tissues revealed that expression of SCP-1 transcripts and antigen selectively in a variety of neoplastic tissues and tumor cell lines.

ICC/IC analysis of SCP1 in mouse pachytene preparation. ICC/IC analysis of SCP1 in mouse pachytene preparation.

Immunofluorescence with specific antiserum demonstrated a...

ABCG2: A Tumor Protector

Thursday, January 31, 2013 - 10:35

ABCG2 is a member of the ATP-binding cassette (ABC) transporter superfamily. Among ABC transporters ABCG2 is particularly interesting for its potential role in protecting cancer stem cells and its complex oligomeric structure (1). The ABC transporters participate in diverse cellular processes, including drug resistance and metabolism, transport of lipids and organic anions, and iron metabolism, while ABCG1, ABCG4, ABCG5, and ABCG8 are involved in the ATP-dependent translocation of steroids and, possibly, other lipids. ABCG2 is expressed exclusively in the plasma membrane and has been identified to confer resistance to anthracycline anticancer drugs, and is expressed in both malignant and normal tissues (2).

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Luciferase: Shining a Light to See Inside Living Animal Models

Wednesday, January 30, 2013 - 16:11

The luciferase reporter is a valuable tool for research into physiology and disease. Light emitted from luciferase enables the monitoring of xenografted tumors, specific cell types, gene expression and pathogens within live animals over time using bioluminescence imaging (BLI) technology. Further detail can be revealed through the use of luciferase antibodies.

Luciferases are a class of enzymes (produced by a variety of organisms) that generate light by acting on substrates (called luciferins). This is a form of chemiluminescence, where the source of the energy emitted as a photon is a chemical reaction, as opposed to absorption of light as in fluorescence.

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Could Laminin be Used to Treat Duchenne Muscular Dystrophy?

Monday, January 28, 2013 - 12:40

Duchenne muscular dystrophy (DMD) is a severe muscle wasting condition, causing disability and early death. There is currently no cure or adequate treatment for DMD, but pioneering research indicates that injection of a laminin protein may prevent (or at least slow) this muscle degeneration.

Around 1 in 3,500 boys are born with DMD. Their muscles become progressively weaker, leading to restricted mobility, and death in their twenties from heart/respiratory failure. Effective therapies for DMD are urgently needed. Mutations in the dystrophin gene result in the lack of this protein in DMD patients. An understanding of the role of dystrophin in normal muscle has enabled the investigation of ways to compensate for its absence.

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RPE65: Vision, Blindness and Hope

Thursday, January 24, 2013 - 10:35

Retinal pigment epithelium-specific 65 kDa protein (RPE65) is an essential vision protein, and so mutations in the RPE65 gene cause blindness. However, clinical trials using gene therapy to treat patients with a defective RPE65 gene suggest that some vision may be restored.

Our eyes detect light via pigments in rod and cone photoreceptor cells. These pigments consist of an opsin protein (a 7-transmembrane, G protein-coupled receptor) with a bound 11-cis retinal chromophore. The 11-cis retinal is the photosensitive component, undergoing photoisomerization to all-trans-retinal. This induces a conformational change in the opsin, activating it and initiating a signal transduction cascade. The 11-cis form of the retinal must be...

xCT: Friend or Foe?

Wednesday, January 23, 2013 - 10:57

There are two opposing sides to the controversial cysteine/glutamate antiporter. On one hand, it can be viewed a guardian of the cell, protecting it from the damaging oxidative stress that can cause cell death and even cancer. But, conversely, it has a dark side, actually facilitating cancer in a number of ways.

The cystine/glutamate antiporter, system xc,  transports cystine into the cell and glutamate out of the cell in a 1:1 ratio. It is composed of two subunits: xCT (also known as SLC7A11) is responsible for the substrate specificity and transport activity, and CD98 (also called 4F2hc or SLC3A2) is involved in directing the heterodimer to the plasma membrane.

Cysteine is required not only for protein biosynthesis, but most significantly is the rate-limiting precursor in the biosynthesis of the...

Somatostatin Receptor 2: Treating Patients Who Cannot Stop Growing

Monday, January 21, 2013 - 09:44

Acromegaly is a rare life-shortening disease caused by elevated levels of growth hormone (GH) secreted by a tumor on the pituitary gland. Treatments include somatostatin analogs, which activate somatostatin receptor 2 (SSTR2), reducing GH secretion and tumor size.

Acromegaly progresses slowly, commonly going years before diagnosis. The first signs of acromegaly are often the changes to the sufferer’s physical appearance. The hands and feet enlarge, leading to increased ring and shoe sizes. The face gradually becomes disfigured – characteristic features of acromegaly patients are a protruding jaw and brow, enlarged tongue and nose, thickened lips, and spacing between teeth. Other possible symptoms include a deepening of the voice, increased perspiration, carpal tunnel syndrome, and sleep apnea. Acromegaly can lead to...

Caspase 9 and Mitochondrial Apoptosis Regulation

Friday, January 18, 2013 - 07:30

Caspase 9 (also termed ICE-LAP6, Mch6, Apaf-3) is a member of cysteine protease family of caspases and is encoded by the CASP9 gene in humans. Caspase-9 is involved in mitochondrial apoptosis pathway and is an initiator caspase. Pro-caspase-9 is activated when binding with Apaf-1 via their respective N-terminal CED-3 homologous domains in the presence of dATP and Cytochrome c (1). Activated Caspase-9 then cleaves downstream pro-Caspase 3 and Caspase 7 and initiates apoptosis cascade which leads to DNA fragmentation and cell death.

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Caspase 7: The Cell's Suicide Switch

Thursday, January 17, 2013 - 11:08

Caspase 7 (also known as CASP7, Mch3, ICE-LAP3, CMH-1) is a member of caspase family of cysteine proteases. It is an apoptosis-related cystein peptidase encoded by the CASP7 gene in humans. CASP7 homologous sequences have been identified in nearly all mammals. Similar to Caspase 3, Caspase-7 is an effector caspase and plays a key role in apoptotic execution. Once activated, Caspase-7 cleaves and activates downstream substrates, such as poly ADP-ribose polymerase (PARP), and causes cellular morphological and biomedical changes associated with apoptosis. During apoptosis, Caspase-7 is activated by initiator caspases (Caspase 8, Caspase 9 and Caspase 10) through...

TLR9, Infectious Disease and Cancer

Monday, January 14, 2013 - 08:22

Toll-like receptor 9 (TLR9) is a protein encoded by TLR9 gene in humans. It is also known as cluster of differentiation 289 (CD289) and is a member of TLR family. Proteins from TLR family are transmembrane proteins that expressed in both antigen-resenting cells (APCs, such as dendritic cells, macrophages and natural killer cells) and non-APCs.  TLRs are located on the cell surface and the endocytic compartment and recognize pathogen-associated molecular patterns (PAMPs), which are specific to infectious pathogens (e.g. viruses, bacteria and fungi). This pattern recognition then leads to signaling pathways that induce the secretion of pro-inflammatory cytokines.

TLR9 specifically recognizes bacterial CpG DNA sequences (CpG-DNA) or synthetic oligodeoxynucleotides containing unmethylated CpG (CpG-ODN) (1). By studying the...

TLR7 and Immune Response Regulation

Thursday, January 10, 2013 - 16:57

Toll-like receptor 7 (TLR7) is a protein encoded by the TLR7 gene in humans and is a member of TLR family. TLRs controls host immune response against pathogens (e.g. viruses, bacteria and fungi) through recognition of pathogen-associated molecular patterns (PAMPs) which are specific to the microorganisms. These pathogen-associated molecular markers are class-specific and mutation-resistant and may be composed of proteins, carbohydrates, lipids, nucleic acids and/or combinations. Recognition of PAMPs by TLRs leads to a series of signaling events resulting in the production of cytokines necessary for the development of effective immunity.

The natural ligands of TLR7 were recently identified as single-stranded RNA (ssRNA), such as ssRNA from influenza viruses (2). The interaction between viral ssRNA and TLR7 occurs in an endosomal compartment in the cell...

RAD51: The cell's 'Mr. Fix-it'

Wednesday, January 9, 2013 - 11:04

RAD51 is a recombinase protein encoded by RAD51 gene in humans. Human RAD51 family members are highly similar to bacterial RecA and yeast Rad51, both biochemically and structurally. It is a 339-amino acid protein that plays an important role in homologous recombination (HR) of DNA during double-strand break (DSB) repair.

DSBs may be the most disruptive form of DNA damage. If left unrepaired, they lead to broken chromosomes and cell death. If repaired improperly, they can result in chromosome translocations and cancer (1).  Homologous recombination is the major pathway to repair DSBs during S phase to G2 phase of the cycle, using the sister chromatid as the repair template. Upon DSB formation, the broken DNA end(s) are processed and resected prior to loading of RAD51. Strand...

GAP43: The learning protein?

Tuesday, January 8, 2013 - 10:56

Growth Associated Protein 43 (GAP43), also termed B-50, F1 or P-57, is a neuron-specific cytoplasmic protein encoded by the GAP-43 gene in humans. The expression of GAP 43 is associated with neural development and synaptic plasticity. A high level of GAP43 expression is observed in neuronal growth cones during development, at axonal regeneration after injury and is phosphorylated after long-term potentiation (1).

IF analysis of GAP43 in a mature retinal ganglion cell demonstrating axon outgrowth.

GAP43 protein is considered a crucial component of the axon and presynaptic terminal. GAP-43 knockout mice have been generated for the study of GAP-43 functions. Homozygous knockout...

SM047 is a Marker for Ovarian Adenocarcinoma

Thursday, January 3, 2013 - 09:19

 Ovarian carcinoma is disease that eludes early diagnosis and has a high mortality rate. In a diagnosis of ovarian carcinoma, one of the most common problems is to distinguish between a primary ovarian and colorectal adenocarcinoma (1). The SM047 antibody, is the product of hybridoma cells derived by fusion of SP2 myeloma cells with splenic lymphocytes of a mouse that had been immunized with a membrane preparation of an ovarian serous cystadenocarcinoma.

Immunofluorescence: SM047 Antibody

The antibody SM047 binds to an epitope that is displayed by a...

Actin Dynamics and Endocytic Trafficking

Wednesday, December 19, 2012 - 15:52

Actin is a ubiquitous and an essential component of the cytoskeleton, with critical roles in a wide range of cellular processes. It is abundant protein whose monomers polymerize into polarized actin filaments, within epithelial cells. Filamentous actin is concentrated at the plasma membrane where a wide variety of actin-associated proteins harness the potential and structure of actin filaments to moderate functions at the plasma membrane (1).

IHC analysis of Actin in human tonsil tissue IHC analysis of Actin in human tonsil tissue

These functions include structural support of the plasma membrane, cell polarity, membrane protein...

PGC-1 alpha: Roles in Mitochondrial Biogenesis and Disease

Monday, December 17, 2012 - 13:04

An important aspect of mitochondria maintenance includes biogenesis to replenish damaged and degraded mitochondrial structures. The regulation of mitochondrial biogenesis is very complex and numerous genes regulate and synchronize protein synthesis from the mitochondrial and nuclear genome. The factors governing these processes include nuclear respiratory factors (NRF1 and NRF2) as well as the nuclear receptors such as peroxisome proliferator receptors (PPARs) and estrogen related receptors (ERRs). Peroxisome proliferator-activated receptor-gamma coactivator alpha (PGC-1 alpha) binds to NRF1 and NRF2, as well as the nuclear receptors PPAR and ERR, to induce expression of their target genes.

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Bulk Antibody & Protein Ordering

Wednesday, December 12, 2012 - 08:23

Novus offers discounts for bulk antibody and protein purchases. Get all your questions answered to help you with your next bulk order.

How do I place a bulk order?
Contact the Novus team by phone or email bulk@novusbio.com

  • US office: 1-888-506-6887 (8 am-8 pm EST Mon-Thurs, 8 am-7 pm EST Fri)
  • Canada office: 855-668-8722 (8 am-5 pm EST Mon-Fri)
  • Europe office: +44 (0) 1223 426001 (8 am-5 pm GMT Mon-Fri)

Additionally, all of our datasheets contain a link for a bulk quote. This will take you to a form to fill out all the requirements for your order.

What information do you need to provide a bulk quote?
In order to provide you with the most accurate quote we will need the following information:

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O-GlcNAc, Glucose Deprivation and Cancer

Monday, December 10, 2012 - 11:07

O-linked beta-N-acetylglucosamine (O-GlcNAc) is a sugar attachment to serine or threonine hydroxyl moieties on nuclear and cytoplasmic proteins. O-GlcNAc modified proteins are generally either cytoplasmic or nuclear proteins, and unlike asparagine-linked or mucin-type O-glycosylation, O-GlcNAc is not further processed into a complex oligosaccharide. In many ways, O-GlcNAc is similar to protein phosphorylation; for example the sugar can be attached or removed dynamically in response to changes in the cellular environment triggered by stress, hormones, or nutrients (1).

WB analysis of O-GlcNAc in in 1) HeLa, 2) NTERA-2, 3) PC-12 and 4) COS-7 cell lysates

Recently,...

AKAP95/AKAP8 Orchestrates and Synchronizes Cellular Events

Friday, December 7, 2012 - 11:58

A-kinase anchor proteins (AKAPs), such as AKAP95/AKAP8, are scaffold proteins that contain a binding domain for the RI/RII subunit of protein kinase A (PKA). AKAPs orchestrate and synchronize cellular events by tethering the cAMP-dependent PKA and other signaling enzymes to organelles and membranes. This gene encodes a nuclear A-kinase anchor protein that binds to the RII alpha subunit of PKA and may play a role in chromosome condensation during mitosis (1).

IHC analysis of IHC AKAP95/AKAP8 in human ovarian cancer

In a recent study the subcellular localization of human...

Cerebellar Degeneration-Related Protein 2 (CDR2): Cell-Cycle Regulated Tumor Antigen

Wednesday, December 5, 2012 - 10:23

CDR2 is a tumor antigen expressed in a high percentage of breast and ovarian tumors and is the target of a naturally occurring tumor immune response in patients with paraneoplastic cerebellar degeneration. CDR2 has also been shown to be a cell cycle regulated protein in tumor cells with protein levels peaking in mitosis (1). Loss of CDR2 in cells has been linked to aberrant mitotic spindle formation and impaired proliferation. Conversely, CDR2 overexpression is also responsible for cell proliferation in tumors.

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