Antibody News

MUC4 (Mucin-4)

Monday, October 6, 2014 - 14:35

Mucus is the viscous secretion that covers epithelial surfaces (trachea, colon, and cervix) and consists of twenty highly glycosylated proteins called mucins. The mucin family all are high-molecular weight proteins with oligosaccharides attached to the serine or threonine residues of their core protein backbone by O-glycosidic linkages. Mucins play fundamental roles in mucosal cell protection, lubrication, and communication with their external environment as detailed by Corfield1. They have been implicated in epithelial renewal and differentiation. There are two distinct categories of mucins: transmembrane mucins (MUC1, MUC3, MUC4, MUC12, MUC13, MUC15, MUC16, MUC17, MUC20 and MUC21) and secreted mucins (MUC2, MUC5AC, MUC5B, MUC6, MUC7, and MUC19).  MUC4 in particular is normally expressed in epithelial tissues including respiratory, colonic, and...

Virus Appreciation Day Infographic

Friday, October 3, 2014 - 13:03

Viruses infect host cells with their genetic material and then reproduce. They are found in humans, plants, bacteria and other places where they can infect cells, adapt and change. In celebration of Virus Appreciation Day, a day discover more about viruses, learn more about viruses in our infographic. virus appreciation day By: Lisa Ikariyama & Kim Mesman Download the PDF version of the Virus Appreciation Day Infographic. Resources:

  1. Scientific American
  2. Virology.ws 
  3. ...

Cyanine (Cy)

Thursday, October 2, 2014 - 15:00

Cyanine dyes are members of the polymethine synthetic dye family historically used to increase photographic emulsion sensitivity. Cyanine dyes have versatile applications and are commonly used as fluorescent labels for proteins, nucleic acids, and small molecules. They are particularly suited for biomedical imaging, protein-protein interactions, proteomics, and transcriptomics. Different variants have distinctive spectral properties – for example, Cyanine dye 7 (Cy7) has a strong absorption peak at 747nm while Cyanine dye 5.5 (Cy5.5) has a strong absorption peak at 675nm. Lightning-Link Cy Antibody Labeling kits are highly-controlled, sophisticated yet fast conjugation systems that simplify immunoassay techniques (Western blotting, ELISA, and immunohistochemistry). The cyanine antibody  was employed to compare the performance and reliability of fluorescent-linked...

Fas - One of pathways toward death

Wednesday, October 1, 2014 - 15:07

Fas is a member of the tumor necrosis factor (TNF)-receptor superfamily and plays a key role in the physiological regulation of programmed cell death. This receptor contains a death domain which enables the formation of a signaling complex that includes Fas-associated death domain protein (FADD), caspase 8, and caspase 10. The auto-proteolytic processing of these complexed caspases triggers a downstream cascade that leads to membrane-mediated apoptosis. Fas also appears to activate NF-kB. The functional impairment of the Fas and Fas Ligand system is associated with the development and progression of malignancies and immune system diseases.

CD56 + NCAM1 (Cluster of differentiation 56 + neural cell adhesion molecule 1)

Monday, September 29, 2014 - 14:30

CD56 is a member of the Ig super family and comprises five Ig-like domains and two extracellular fibronectin-type III domains. It is expressed as three major isoforms within the nervous system, on NK cells, and a specific set of T-cells. CD56+ NK and T-cells are unique in their ability to mediate cell-mediated cytotoxicity against certain tumor cell targets without MHC restriction. Other CD56 physiological functions include: mediating cell adhesion, triggering neurite extension and migration, and brain synapse formation. CD56 is also crucial for neuronal development and plasticity in the adult brain. It is used as a tumor marker in various cancers (NK lymphomas and Merkel cell carcinoma). As another member of the Ig super family superfamily, NCAM1 consists of five extracellular Ig-like domains and two fibronectin type III domains. It has at least 20-30 distinct isoforms due to alternative splicing and sialylation posttranslational modifications.

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CD34 (Cluster of differentiation 34, hematopoietic progenitor cell antigen)

Friday, September 26, 2014 - 13:54

CD34 is a cell-surface glycoprotein type 1 transmembrane protein that belongs to the sialomucin family. CD34 comprises of an intracellular cytoplasmic domain with consensus sites for serine, threonine, tyrosine and active protein kinase C (PKC). Because it is differentially glycosylated within different cell types, it has a range of apparent molecular weight sizes. It is a marker for pluripotent hematopoietic stem or progenitor cells and has been extensively used to isolate and characterize these progenitor cells. CD34 is also expressed on vascular endothelium, bone marrow stroma, embryonic fibroblasts, and neurons. As CD34-positive populations expand and differentiate into their destined lymphohematopoietic lineages, they lose their hallmark CD34 expression.

Ovarian Cancer Infographic

Thursday, September 25, 2014 - 13:10

September is Ovarian Cancer Awareness month and brings to focus a cancer that is estimated to be diagnosed in over 21,000 women in the US in 2014 (1). Ovarian cancer often goes undiagnosed due to the lack of symptoms until it metastasized into the pelvic or abdominal areas. Treatment typically requires surgery and chemotherapy.

Ovarian cancer infographic

 

By: Lisa Ikariyama; Design: Kim Mesman

Download our ovarian cancer infographic

References:

  1. Cancer.org 
    ...

PSMA (Prostate specific membrane antigen, Glutamate carboxypeptidase II)

Wednesday, September 24, 2014 - 14:38

Prostate specific membrane antigen (PSMA), also known as Glutamate carboxypeptidase II (GCPII), is a type II transmembrane glycoprotein that belongs to the M28 peptidase family. It acts as a glutamate carboxypeptidase on different substrates such as folate as well as the neuropeptide N-acetyl-l-aspartyl-l-glutamate. PSMA is expressed in a number of tissues including prostate, kidney, and both the central and peripheral nervous systems. A mutation in this gene is associated with impaired intestinal absorption of dietary folates, resulting in low blood folate levels and subsequent hyperhomocysteinemia. Expression of PSMA in the brain may be involved in a number of pathological conditions associated with glutamate excitotoxicity.

Western Blot: PSMA Antibody Western Blot...

GFP - Be Green!

Monday, September 22, 2014 - 14:26

Green fluorescence protein (GFP) is a 27KD protein derived from the jellyfish Aquorea victoria that emits a green light (emission peak at a wavelength of 509 nm) when excited by blue light (excitation peak at a wavelength of 395 nm). GFP is a highly versatile protein that has become an invaluable tool in cell biology research because of its intrinsic fluorescence without substrate requirement, ability to be visualized over time durations - both short- and long-term - in living cells, and short sequence making it easy to clone and use an unobtrusive tag. GFP fluorescence is stable under standard fixation conditions and suitable for a huge variety of applications. Due to all of these advantages, GFP has been widely used as a gene expression reporter and tag, enabling researchers to visualize and localize proteins within living cells without the extra burden or complication of staining.

Integrin beta 1 binding protein 2

Friday, September 19, 2014 - 14:28

ITGB1BP2 is a muscle-specific protein cloned by a rat created by Branccio's group in Italy that was found to interact with the cytoplasmic domain of integrin beta 11. It is expressed only in heart and skeletal muscle but is not essential for normal development and differentiation of these tissues. Branccio's group published a follow-up study in Nature Medicine using an ITGB1BP2 antibody that the protein plays a critical role in sensing mechanical stress due to pressure overloading2. This response protects against subsequent compensatory dilated cardiomyopathy and contractile dysfunction. Further work from this group confirmed that ITGB1BP2 nucleotide variations are found in families of patients with hypertension and/or primary dilated or hypertrophic cardiomyopathy3.

Beta III tubulin

Thursday, September 18, 2014 - 15:42

The Beta III tubulin protein is abundantly present in both the central and peripheral nervous systems (CNS and PNS), where it is predominantly expressed during fetal and postnatal development. In cerebellar and sympathoadrenal neurogenesis, Beta III distribution is neuron-associated and present in distinct temporal-spatial gradients that are dictated by the regional neuroepithelia of origin. In addition, CNS subventricular zones consisting of neuronal and glial precursor cells exhibit transient beta III expression, where it may enable the identification of presumptive neurons derived from embryonic stem cells. In contrast, Beta III distribution is almost exclusively neuron-specific in adult tissues. Researchers published in Cell share their findings that the receptor tyrosine kinase Ret is required for motor axon attraction by integrating diffusible- and contact-axon guidance signaling in a hierarchical GPI-receptor signaling system1.

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CD19: An Undoubted Biomarker for B Cells

Wednesday, September 17, 2014 - 15:16

CD19 is a cell surface protein member of the large immunoglobulin superfamily that complexes with CD21, CD81, and CD225 in the membrane of mature B-cells. A major function of CD19 is to assemble with the antigen receptor of B-lymphocytes to decrease the threshold for receptor-dependent stimulation, thus enhancing the specificity and sensitivity of B-cells towards antigens. CD19 plays a large role in regulating B-cell growth. Its expression is confined to only B-lymphocytes and follicular dendritic cells of the hematopoietic system. Leukemia phenotype studies suggest that CD19 is the earliest and broadest B-cell restricted marker. Because increased CD19 expression stimulates autoantibody production, CD19 studies provide insight into the autoimmunity process.

Glucose-6-phosphatase (G6PC) - A key to regulate your blood sugar level!

Tuesday, September 16, 2014 - 15:17

The integral endoplasmic reticulum membrane-based enzyme G6PC hydrolyzes its substrate glucose-6-phosphate into glucose. Specifically, G6PC breaks down D-glucose 6-phosphate to D-glucose and orthophosphate. Because G6PC forms with the glucose-6-phosphate transporter (SLC37A4/G6PT), the resulting complex is responsible for glucose production. Thus, G6PC is the key enzyme in glucose homeostasis, functioning in both the processes of gluconeogenesis and glycogenolysis. Defects in the enzyme cause glycogen storage disease type I (von Gierke disease). Not surprisingly, G6PC is localized mainly in the liver and kidneys.  It is unique in that it is membrane-bound, unlike most other enzymes that act upon water soluble substrates.

CD14 - TLR4 is my friend in battle against infections!

Monday, September 15, 2014 - 15:37

CD14 is a well-characterized cell-activating receptor for lipopolysaccharide-binding protein (LBP) and peptidoglycan. It is an important modulator for lipopolysaccharide (LPS)-dependent signaling and is a component of the multi-protein complex containing also containing MD2 and toll-like receptor 4 (TLR4). CD14 is an important component of the innate immune response preferentially expressed on mature cells of monocyte lineage. The CD14 protein contains eleven leucine-rich repeats (LRRs). It is also known to be involved in the apoptotic cell clearance, cell surface adhesion molecule upregulation, and IgE level regulation.  It exists in two forms:  a glycosylphosphatidylinositol-anchored membrane protein (mCD14) and a monocyte or liver-derived soluble serum protein (sCD14) which lacks the anchor. sCD14 plays a role in LPS sensitivity to cells lacking the membrane form, and its increased expression is thought to be associated with...

Von Willebrand Factor: An important mediator and carrier of hemostasis

Thursday, September 11, 2014 - 15:44

Human Von Willebrand Factor (factor VIII R: Ag) is a 270 kDa multimeric plasma gylcoprotein. Important in the maintenance of hemostasis, it mediates platelet adhesion to injured vessel walls and serves as a carrier and stabilizer for coagulation factor VIII. The Von Willebrand factor has functional binding domains to platelet glycoprotein Ib, glycoprotein IIb/IIIa, collagen and heparin. The factor is synthesized by endothelial cells and is also present in platelets and megakaryocytes.

The essential biologic properties of VWF have been explicated, particularly in the areas of genetic regulation, biosynthesis, and specific bimolecular interactions. The three-dimensional structure of selected domains has been solved, but our understanding of detailed structure-function relationships is still fragmented because of the complexity and size of the VWF molecule. The biomechanical properties of the interaction between the VWF A1 domain and...

TdT (Terminal Deoxynucleotidyl Transferase)

Monday, September 8, 2014 - 15:13

The enzyme family of DNA polymerases plays a fundamental role in the replication, repair, and recombination of nucleic acid. Its members include DNA Polymerase b (Pol b), DNA Polymerase g (Pol g), and DNA Polymerase m (Pol m). TdT is a very unique and fascinating member of this family because, unlike all other DNA polymerases, TdT synthesizes DNA from only single-stranded DNA. This unusual ability to work in a completely template-independent manner was discovered early on (TdT was one of the first activities found in mammals) but not well understood1. An excellent summary of the history, structure, and function of TdT can be found in Motea and Berdis' review2. It is now evident that such random nucleotide addition allows V(D)J recombination and therefore...

RIG-1 - Notorious RIG

Friday, September 5, 2014 - 14:40

Viral infection triggers the antiviral cell response by activating the innate cellular immune system that recognizes various viral components. One component of this process is the cytoplasmic helicase RIG-1 which is a pattern recognition receptor. Like toll-like receptor 3 (TLR3), RIG-1 recognizes double-stranded (ds) RNA, but unlike TLR3, RIG-1 activates tank-binding kinase 1 (TBK1) and inhibitor of nuclear factor kappa-B kinase subunit epsilon (IKKepsilon) through the adaptor protein known as interferon-beta promoter stimulator 1 (IPS-1). This kinase cascade ultimately phosphorylates the transcription factors interferon regulatory factors 3 and 7 (IRF-3, IRF-7, respectively). Both of these are essential for type-I interferon expression. Not surprisingly, RIG-1 is required for interferon production in response to RNA viruses (paramyxoviruses, influenza virus, and Japanese encephalitis virus, among...

MUL1 - A Mito's best friend

Thursday, September 4, 2014 - 15:54

MUL1 is an E3 ubiquitin-protein ligase with a RING finger domain that controls mitochondrial morphology, fragmentation and localization. E3 ubiquitin ligases accept the component ubiquitin from a donor E2 ubiquitin-conjugating directly transfer this ubiquitin to designated targeted substrates. The largest, proteome-wide and site-specific quantitative mapping dataset assessment of endogenous putative ubiquitylation sites and regulation was executed by Wagner’s group in Denmark1.  Their compelling experiments also evaluated crosstalk between ubiquitylation and acetylation modifications using an MUL1 antibody. When overexpressed, MUL1 activates the JNK signal cascade and induces caspase-dependent apoptosis. MUL1 has also been shown to negatively regulate Akt kinase, suppressing cell proliferation and viability2.

SOX-11 seals your fate

Wednesday, September 3, 2014 - 14:40

The SOX-11 transcription factor is a member of the SOX family known to be involved in embryonic development regulation and cell fate determination. The protein acts as a transcriptional regulator and appears to modulate fundamental aspects of normal embryonic nervous system development and tumorigenesis. SOX-11 is not found expressed in adult tissues except for the adult immature neuron. Ek's group in Sweden employed the SOX11 antibody to develop signatures comprised of mantle cell lymphoma (MCL)-associated genes through a comprehensive expression analysis of both normal and malignant B-cells1. These profiles were created to identify diagnostic and therapeutic targets that are efficient, genome-based modalities for this aggressive lymphoid malignancy. Additional studies that surveyed a wider range of lymphomas relied upon SOX11 antibody immunohistochemistry and widened the prognostic value of...

PIM-1: An Important Oncogene in Multiple Cancers

Friday, August 29, 2014 - 14:40

The PIM-1 (proto-oncogene serine/threonine-protein kinase) protein is an epithelial-derived, integral membrane serine protease. This protease forms a complex with the Kunitz-type serine protease inhibitor, HAI-1, and is activated by sphingosine 1-phosphate. PIM-1 cleaves and activates hepatocyte growth factor/scattering factor (HGF) as well as urokinase plasminogen activator (uPA). Such downstream targets implicate this serine protease as an epithelial membrane trigger for a sequential protease cascade. PIM-1 expression is associated with many tumors including breast, colon, prostate, and ovarian. Hematologists at UCLA used the PIM-1 antibody to characterize the physiological effects of ABT-869, a multi-targeted receptor tyrosine kinase inhibitor1. This group found that ABT-869 blocked FMS-like tyrosine kinase 3-internal tandem duplication (FLT3) phosphorylation, induced apoptosis, decreased proliferation,...

APE1: A Multifunctional Protein

Wednesday, August 27, 2014 - 15:37

AP-endonuclease (APE1/Ref-1) is an essential multifunctional protein involved in the repair of oxidative DNA damage as well as in transcriptional regulation in tumor cells. It functions as an apurinic/apyrimidinic (AP) endodeoxyribonuclease in the DNA base excision repair (BER) pathway of DNA lesions, and may also play a role in the epigenetic regulation of gene expression and the protection from granzymes-mediated cellular repair leading to cell death. APE1 is involved in calcium-dependent down-regulation of parathyroid hormone (PTH) expression by binding to negative calcium response elements (nCaREs).

Melphalan resistance has been considered one of the major obstacles to improve outcomes in multiple myeloma (MM) therapy. A study using Novus’ APE1 antibody, NB100-116, has shown that the acetylation modification of APE1 is involved in melphalan resistance of MM cells and has also shed light on...

FANCD2: A big component of the DNA repair crew

Monday, August 25, 2014 - 13:49

The genetic disorder known as Fanconi anemia (FANC) is a heterogeneous, autosomal-recessive cancer susceptibility condition characterized by a wide array of symptoms. These include congenital malformations, progressive bone marrow failure, DNA-damage hypersensitivity, and genome instability. The protein FANCD2 is a subunit of the protein complex involved in cellular resistance to DNA cross-linking and DNA synthesis arrest triggered by ionizing radiation (IR). The FANCD2 antibody was used in immunoblotting and immunoprecipitation experiments to better understand how processes such as oxidative stress and damage trigger the formation of a multimeric FANC complex within the nucleus1.

Western Blot: FANCD2 Antibody ...

A Double-Edged Sword: GDF15

Friday, August 22, 2014 - 11:04

Bone morphogenetic proteins such as GDF15 belong to the transforming growth factor-beta (TGFB) family that directs tissue differentiation and maintenance. GDF15 appears to be involved in a variety of physiological processes such as pregnancy, injury and inflammation, and apoptosis. Evidence suggests GDF15 is a marker for metastasis. A Swiss group profiled expression of GDF15 via RT-PCR and immunoblotting with the GDF15 antibody in mouse and human glioma cell lines to better correlate tumor grade with proliferative capability and immunogenicity1. Their data clearly showed that endogenous levels of GDF15 cause proliferation and immune escape of glioma cells. Tabrizi et al performed similar profiling studies with the GDF15 antibody in primary ovarian mucinous carcinomas of the intestine2. Based on their studies, they suggest that current and updated diagnostic criteria and standards...

PCSK9: To neuron or not to neuron

Wednesday, August 20, 2014 - 15:36

PCSK9 (Proprotein convertase subtilisin/kexin type 9) is a member of the proteinase K subfamily of the secretory subtilase family. It is first produced as a soluble zymogen that then undergoes an autocatalytic processing within the endoplasmic reticulum (ER). PCSK9 functions in cholesterol homeostasis as well as cortical neuron differentiation. Mutations in this gene are associated with a third form of autosomal dominant familial hypercholesterolemia (HCHOLA3). Blesa’s group used the PCSK9 antibody to study the prevalence of PCSK9 mutations in autosomal dominant hypercholesterolemia (ADH) within a particular Spanish subpopulation1. There were unable to detect any of the previously described mutations they were looking for within this cohort, but identified a novel mutation responsible for increasing PCSK9 transcription. Dube et al employed the PCSK9 antibody in their gestational diabetes...

PINK1 and its role in Parkinson's disease

Tuesday, August 19, 2014 - 15:29

PINK1 (PTEN induced putative kinase 1) is a mitochondrial serine/threonine kinase which maintains mitochondrial function/integrity, provides protection against mitochondrial dysfunction during cellular stress, potentially by phosphorylating mitochondrial proteins, and is involved in the clearance of damaged mitochondria via selective autophagy (mitophagy). PINK1 and its substrates have been found in the cytosol as well as in different sub-mitochondrial compartments.  According to recent reports, PINK1 may be targeted to OMM (outer mitochondrial membrane) with its kinase domain facing the cytosol, providing a possible explanation for the observed physical interaction with the cytosolic E3 ubiquitin ligase Parkin. PINK1 has been linked to autosomal recessive early onset Parkinson's disease, Alzheimer's disease, dementia, multiple sclerosis, schizophrenia, neuronitis, myeloma ect.

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