Technology from Abcam

Similar documents
NEW IHC A n t i b o d i e s

The Panel Approach to Diagnostics. Lauren Hopson International Product Specialist Cell Marque Corporation

Cancers of unknown primary : Knowing the unknown. Prof. Ahmed Hossain Professor of Medicine SSMC

Financial disclosures

Cutaneous Mesenchymal Neoplasms with EWSR1 Rearrangement

Financial disclosures

Disclosures. An update on ancillary techniques in the diagnosis of soft tissue tumors. Ancillary techniques. Introduction

Disclosures. An update on ancillary techniques in the diagnosis of soft tissue tumors. Ancillary techniques. Introduction

Immunohistochemical classification of lung carcinomas and mesotheliomas. Prof. Mogens Vyberg NordiQC Institute of Pathology Aalborg, Denmark

The role of immunohistochemistry in surgical pathology of the uterine corpus and cervix

From Morphology to Molecular Pathology: A Practical Approach for Cytopathologists Part 1-Cytomorphology. Songlin Zhang, MD, PhD LSUHSC-Shreveport

Breast - ductal carcinoma CK7 ER PR GATA3 Mammaglobin (50-70%) GCDFP-15 (50-70%) E-cadherin HMWCK CK20 PAX2 ER/PR/HER2 on all newly diagnosed cases

Financial disclosures

Diagnostic IHC in lung and pleura pathology

DOUBLE STAINS. Toll-Free: Direct:

Applications of IHC. Determination of the primary site in metastatic tumors of unknown origin

IHC Panels as an Aid in Diagnostic Decision Making

Charles Halsey, DVM, PhD, DACVP Pfizer, Inc. IHC Resources

ONCOLOGY. Csaba Bödör. Department of Pathology and Experimental Cancer Research november 19., ÁOK, III.

3/24/2017 DENDRITIC CELL NEOPLASMS: HISTOLOGY, IMMUNOHISTOCHEMISTRY, AND MOLECULAR GENETICS. Disclosure of Relevant Financial Relationships

C.L. Davis Foundation Descriptive Veterinary Pathology Course

FOLLICULARITY in LYMPHOMA

Case: The patient is a 73 year old woman with vague complaints of dyspepsia and abdominal pain. Upper endoscopy showed features of gastritis and a

Single and Multiplex Immunohistochemistry

Lung Tumor Cases: Common Problems and Helpful Hints

ACCME/Disclosures. Diagnosing Mesothelioma in Limited Tissue Samples. Papanicolaou Society of Cytopathology Companion Meeting March 12 th, 2016

Kimberly Rohan ANP-BC, AOCN Nurse Practitioner Edward Cancer Center

Presentation material is for education purposes only. All rights reserved URMC Radiology Page 1 of 98

NEOPLASIA-I CANCER. Nam Deuk Kim, Ph.D.

External Quality Assessment of melanocytic marker analyses NordiQC experience

4/12/2018. MUSC Pathology Symposium Kiawah Island April 18, Jesse K. McKenney, MD

Immunohistochemical Evaluation of Necrotic Malignant Melanomas

Tumores de células pequeñas, redondas y azules: diagnóstico diferencial cuando el tiempo apremia

Classification of the unknown primary tumour: the primary IHC panel

TEST MENU BY SPECIALTY

Schedule of Accreditation issued by United Kingdom Accreditation Service 2 Pine Trees, Chertsey Lane, Staines-upon-Thames, TW18 3HR, UK

Immunohistochemical classification of the unknown primary tumour (UPT) Part I. Prof. Mogens Vyberg NordiQC Institute of Pathology Aalborg, Denmark

57th Annual HSCP Spring Symposium 4/16/2016

Breast cancer: IHC classification. Mogens Vyberg Professor of Clinical Pathology Director of NordiQC Aalborg University Hospital, Aalborg, Denmark

Cutaneous metastases. Thaddeus Mully. University of California, San Francisco Professor, Departments of Pathology and Dermatology

Immunopathology of Lymphoma

Review and Updates of Immunohistochemistry in Selected Salivary Gland and Head and Neck Tumors

Enterprise Interest Nothing to declare

Mody. AIS vs. Invasive Adenocarcinoma of the Cervix

Tumour Structure and Nomenclature. Paul Edwards. Department of Pathology and Cancer Research UK Cambridge Institute, University of Cambridge

Test Bank for Robbins and Cotran Pathologic Basis of Disease 9th Edition by Kumar

Desmoplastic Melanoma R/O BCC. Clinical Information. 74 y.o. man with lesion on left side of neck r/o BCC

What I Learned from 3 Cases and 3 Antibodies

Catalog Supplement. Vol. 10.1

CODING TUMOUR MORPHOLOGY. Otto Visser

Test Bank for Robbins and Cotran Pathologic Basis of Disease 9th Edition by Kumar

7 Omar Abu Reesh. Dr. Ahmad Mansour Dr. Ahmad Mansour

Pathology Mystery and Surprise

Diplomate of the American Board of Pathology in Anatomic and Clinical Pathology

MEDICAL POLICY Gene Expression Profiling for Cancers of Unknown Primary Site

Differential diagnosis of HCC

Gastric Carcinoma with Lymphoid Stroma: Association with Epstein Virus Genome demonstrated by PCR

Dr Rodney Itaki Lecturer Anatomical Pathology Discipline. University of Papua New Guinea School of Medicine & Health Sciences Division of Pathology

New Developments in Immunohistochemistry for Gynecologic Pathology

Differential diagnosis of hematolymphoid tumors composed of medium-sized cells. Brian Skinnider B.C. Cancer Agency, Vancouver General Hospital

Tumor Markers Yesterday, Today & Tomorrow. Steven E. Zimmerman M.D. Vice President & Chief Medical Director

What is New in the 2015 WHO Lung Cancer Classification? Zhaolin Xu, MD, FRCPC, FCAP

Neoplasia part I. Dr. Mohsen Dashti. Clinical Medicine & Pathology nd Lecture

The unkown primary tumour: IHC Classification, antibody selection, protocol optimization, controls and EQA (part I)

Mesothelioma: diagnostic challenges from a pathological perspective. Naseema Vorajee August 2016

Computational Systems Biology: Biology X

Pancreas. Atrophy, acinar cell. Pathogenesis: Diagnostic key features:

Neoplasia literally means "new growth.

Carcinoma of Unknown Primary (CUP)

Review of the AP Part II Practical Examination. Dr David Clift Co Chief Examiner

In Situ Hybridization Immunohistochemistry

ACR TXIT TM EXAM OUTLINE

Carcinoma of unknown primary origin (CUP) is defined

Nordic Immunohistochemical Quality Control

SHN-1 Human Digestive Panel Test results

ADVANCED STAINING PRODUCT CATALOG. In Situ Hybridization Probes Immunohistochemistry Antibodies Detection Systems Ancillary Reagents

TUMOR M ARKERS MARKERS

The unknown primary tumour: IHC classification part I, the primary panel - Antibody selection, protocol optimization, controls and EQA

Role of immunohistochemistry in the differential diagnosis of malignant small round cell tumor: a study of 38 cases

Oncocytic-Appearing Salivary Gland Tumors. Oncocytic, Cystic, Mucinous, and High Grade Salivary Gland Tumors SALIVARY GLAND FNA: PART II

Cerebral Parenchymal Lesions: I. Metastatic Neoplasms

The clinically challenging entity of liver metastasis from tumors of unknown primary

Biopsy Interpretation of Spindle cell proliferations of the Serosa

Urinary Bladder: WHO Classification and AJCC Staging Update 2017

The Development of Lymphocytes: B Cell Development in the Bone Marrow & Peripheral Lymphoid Tissue Deborah A. Lebman, Ph.D.

Classification (1) Classification (3) Classification (2) Spindle cell lesions. Spindle cell lesions of bladder (Mills et al.

Pitfalls in thyroid tumor pathology. Prof.Valdi Pešutić-Pisac MD, PhD

Immunohistochemistry in Bone and Soft Tissue Tumors. Sahar Rassi Zankoul, MD

Tumor Markers & Cytopathology

Schedule of Accreditation issued by United Kingdom Accreditation Service 2 Pine Trees, Chertsey Lane, Staines-upon-Thames, TW18 3HR, UK

Chapter 9, Part 1: Biology of Cancer and Tumor Spread

Histopathological diagnosis of CUP

Section 14 Other Cancers. Cancer of Unknown 113 Primary Site INTRODUCTION PATHOLOGIC EVALUATION

Plasma cell myeloma (multiple myeloma)

MT09 - Normal Human Tissue Microarray, FDA

Neoplasia 2018 lecture 11. Dr H Awad FRCPath

performed to help sway the clinician in what the appropriate diagnosis is, which can substantially alter the treatment of management.

Objectives. Salivary Gland FNA: The Milan System. Role of Salivary Gland FNA 04/26/2018

Surgical Pathology Evening Specialty Conference USCAP 2015

How to Recognize Gynecologic Cancer Cells from Pelvic Washing and Ascetic Specimens

Transcription:

CD2 (EP222) CD2 is one of the earliest T-cell lineage restricted antigens to appear during T-cell differentiation and only rare CD2+ cells can be found in the bone marrow. Anti-CD2 is a pan-t-cell antigen marker. Anti-CD2 is therefore useful for the identification of virtually all normal T-lymphocytes. It is also very useful in the assessment of lymphoid malignancies as it is expressed in the majority of precursor and mature T-cell lymphomas and leukemias. As with other pan-t-cell antigens, CD2 may be aberrantly deleted in some neoplastic T-cell populations, especially peripheral T-cell lymphomas. When combined with anti-cd25, anti-cd2 may assist in the identification of systemic mastocytosis and mastocytic leukemia. Above: Anti-CD2 stains angioimmunoblastic T-cell lymphoma cells in cytoplasmic and perinuclear Golgi pattern. 0.1 ml, concentrate...102r-14 0.5 ml, concentrate...102r-15 1 ml, concentrate...102r-16 1 ml, prediluted...102r-17 7 ml, prediluted...102r-18 Positive control slides...102s, membranous Control Tonsil Desmin (EP15) Anti-desmin detects a protein that is expressed by cells of normal smooth, skeletal, and cardiac muscles. It has been suggested that desmin is primarily located at or near the periphery of Z lines in striated muscle fibrils. In smooth muscle, desmin interconnects cytoplasmic dense bodies with membrane bound dense plaques. Anti-desmin reacts with leiomyomas, leiomyosarcoma, rhabdomyomas, rhabdomyosarcoma, and perivascular cells of glomus tumors of the skin. This antibody is used to demonstrate the myogenic components/derivation of tumors. Desmin can also be present in myofibroblasts and be focally positive in desmoid fibromatosis. Above: Anti-desmin highlights rhabdomyosarcoma cells in a cytoplasmic pattern. 0.1 ml, concentrate...243r-14 0.5 ml, concentrate...243r-15 1 ml, concentrate...243r-16 1 ml, prediluted...243r-17 7 ml, prediluted...243r-18 Positive control slides...243s Control Skeletal muscle 2

ERG (EP111) ERG is a member of the erythroblastosis virus E26 transforming sequence (ETS) transcription factor gene family, which also includes FLI-1 and ETS-1. ERG is expressed in lymphocytes and endothelial cells and regulates endothelial apoptosis and angiogenesis. ERG has been found to be expressed in both benign and malignant vascular tumors. Anti-ERG was found to have high sensitivity for vascular neoplasms. ERG expression has been observed in prostate carcinomas and high-grade prostatic intraepithelial neoplasia (HGPIN). ERG positivity in any other epithelial tumor other than prostate carcinoma is extremely rare. In a study of all carcinomas of the breast, gastrointestinal tract, gynecologic system, kidney, lung, ovary, pancreas, salivary glands, skin, thyroid, and testis were negative for ERG. ERG has also been observed to be positive in a minority of Ewing sarcomas. This is caused by a chromosomal rearrangement which fuses the EWSR1 gene with the ERG gene (EWSR 1:ERG). ERG has also been observed to stain some meningiomas due to cross reactivity with FLI-1. Above: Anti-ERG decorates nuclei of prostatic carcinoma. 0.1 ml, concentrate...434r-14 0.5 ml, concentrate...434r-15 1 ml, concentrate...434r-16 1 ml, prediluted...434r-17 7 ml, prediluted...434r-18 Positive control slides...434s Visualization Nuclear Control Tonsil, hemangioma FSH (EP257) Follicle-stimulating hormone (FSH) is a member of the pituitary glycoprotein hormone family which includes luteinizing hormone, chorionic gonadotropin, and thyroid-stimulating hormone. Follicle-stimulating hormone enables ovarian folliculogenesis to the antral follicle stage and is essential for Sertoli cell proliferation and maintenance of sperm quality in the testis. Members of the pituitary glycoprotein hormone family consist of a shared alpha chain and a beta chain encoded by a separate gene. The FSHB gene encodes the beta subunit of follicle stimulating hormone. Anti-FSH is a useful marker in classification of pituitary tumors and the study of pituitary disease, as it reacts with FSH-producing cells (gonadotrophs). Above: Rabbit monoclonal anti-fsh displays pituitary adenoma cells. 0.1 ml, concentrate...207r-14 0.5 ml, concentrate...207r-15 1 ml, concentrate...207r-16 1 ml, prediluted...207r-17 7 ml, prediluted...207r-18 Positive control slides...207s Control Pituitary 3

Granzyme B (EP230) Granzymes are serine proteases, which are stored in specialized lytic granules of cytotoxic T-lymphocytes and in natural killer cells. Anti-granzyme B has been useful in the identification of natural killer/t-cell lymphoma, as well as anaplastic large cell lymphoma. Above: Anti-granzyme B shows cytotoxic granules in the cytoplasm of angioimmunoblastic T-cell lymphoma cells. 0.1 ml, concentrate...262r-14 0.5 ml, concentrate...262r-15 1 ml, concentrate...262r-16 1 ml, prediluted...262r-17 7 ml, prediluted...262r-18 Positive control slides...262s Control Spleen, anaplastic large cell lymphoma Kappa (EP171) Anti-kappa detects surface immunoglobulin on normal and neoplastic B-cells. In paraffin-embedded tissue, anti-kappa exhibits strong staining of kappa-positive plasma cells and cells that have absorbed exogenous immunoglobulins. When dealing with B-cell neoplasms, the determination of light chain ratios remains the centerpiece. Most B-cell lymphomas express either kappa or lambda light chains, whereas reactive proliferations display a mixture of kappa and lambda positive cells. If only a single light chain type is detected, a lymphoproliferative disorder exists. Above: Anti-kappa light chain demonstrates kappa producing plasma cells in the tonsilar tissue. 0.1 ml, concentrate...274r-14 0.5 ml, concentrate...274r-15 1 ml, concentrate...274r-16 1 ml, prediluted...274r-17 7 ml, prediluted...274r-18 Positive control slides...274s Control Tonsil 4

Lambda (EP172) Anti-lambda detects surface immunoglobulin on normal and neoplastic B-cells. Anti-lambda staining is seen in B-cell follicles of human lymphoid tissue. When dealing with B-cell neoplasms, the determination of light chain ratios remains helpful. Most B-cell lymphomas express either kappa or lambda light chains, whereas reactive proliferations display a mixture of kappa and lambda positive cells. If only a single light chain type is detected, a lymphoproliferative disorder is very likely. Above: Plasma cells in the tonsil are highlighted by the anti-lambda light chain. 0.1 ml, concentrate...277r-14 0.5 ml, concentrate...277r-15 1 ml, concentrate...277r-16 1 ml, prediluted...277r-17 7 ml, prediluted...277r-18 Positive control slides...277s Control Tonsil Mammaglobin (EP249) Mammaglobin (10 kd) is a breast-associated glycoprotein distantly related to secretoglobin family that includes human uteroglobin and lipophilin. Mammaglobin mrna is present in high levels in human breast cancer cell lines, which has been shown to be a sensitive marker of breast cancer. When combined with other breast-restricted markers such as GCDFP-15, an overall sensitivity for breast carcinoma of 84% has been achieved. Anti-mammaglobin can also be used to determine breast origin in the setting of metastatic carcinoma. Above: Anti-mammaglobin illustrates the protein expression in the cells of invasive ductal carcinoma of the breast. 0.1 ml, concentrate...280r-24 0.5 ml, concentrate...280r-25 1 ml, concentrate...280r-26 1 ml, prediluted...280r-27 7 ml, prediluted...280r-28 Positive control slides...280s Control Breast carcinoma 5

Napsin A (EP205) Napsin is a pepsin-like aspartic proteinase, in the A1 clan of the AA clade of proteinases. There are two closely related napsins, napsin A and napsin B. Napsin A is expressed as a single chain protein with the molecular weight of approximately 38 kda. Immunohistochemical studies revealed high expression levels of napsin A in human lung and kidney but low expression in spleen. Napsin A is expressed in type II pneumocytes and in adenocarcinomas of lung. The high specificity expression of napsin A in adenocarcinomas of lung is useful to distinguish primary lung adenocarcinomas from adenocarcinomas of other organs. Above: Lung adenocarcinoma is strongly and diffusely positive for anti-napsin A. 0.1 ml, concentrate...352r-14 0.5 ml, concentrate...352r-15 1 ml, concentrate...352r-16 1 ml, prediluted...352r-17 7 ml, prediluted...352r-18 Positive control slides...352s Control Lung adenocarcinoma, kidney, renal cell carcinoma SOX-10 (EP268) Sry-related HMG-BOX gene 10 (SOX-10) is a nuclear transcription factor that participates in neural crest development and in the specification and differentiation of cells of melanocytic lineage. It has been recently shown to be a sensitive marker of melanoma, including conventional, spindled, and desmoplastic subtypes. SOX-10 was expressed by metastatic melanomas in sentinel lymph nodes, but not by other lymph node components such as dendritic cells, which usually express S100 protein. Anti-SOX-10 has been shown to be superior to all other immunostains in detecting residual invasive and in situ melanoma. Anti-SOX-10 is also a useful marker in detecting both the in situ and invasive components of desmoplastic melanoma. It is known that the commonly used melanoma markers, anti-hmb-45 and anti-melan A, are poorly expressed in desmoplastic melanomas while it has been reported that anti-sox-10 was moderately to strongly expressed in almost all desmoplastic melanomas. SOX-10 is diffusely expressed in schwannomas and neurofibromas. SOX-10 presence was not identified in any other mesenchymal and epithelial tumors except for myoepitheliomas and diffuse astrocytomas. Above: SOX-10 rabbit monoclonal antibody highlights tumor cells of desmoplastic melanoma. 0.1 ml, concentrate...383r-14 0.5 ml, concentrate...383r-15 1 ml, concentrate...383r-16 1 ml, prediluted...383r-17 7 ml, prediluted...383r-18 Positive control slides...383s Visualization Nuclear Control Melanoma, skin melanocytes 6

TTF-1 (EP229) Anti-TTF-1 (Thyroid Transcription Factor 1) is useful in differentiating primary adenocarcinoma of the lung from metastatic carcinomas originating in the organs rather than thyroid, germ cell tumors, and malignant mesothelioma. It can also be used to differentiate small cell lung carcinoma from lymphoid infiltrates. TTF-1 labeling is also seen in thyroid and thyroid-derived tumors. TTF-1 immunostaining is useful in the differentiation between pulmonary and nonpulmonary origin of adenocarcinomas in malignant effusions. TTF-1 staining is very reliable in discerning whether a brain metastasis has arisen from a pulmonary or nonpulmonary site, particularly when dealing with adenocarcinomas and large cell carcinomas. Above: Lung adenocarcinoma strongly and diffusely express TTF-1 protein in the nuclei of the tumor cells. 0.1 ml, concentrate...343r-14 0.5 ml, concentrate...343r-15 1 ml, concentrate...343r-16 1 ml, prediluted...343r-17 7 ml, prediluted...343r-18 Positive control slides...343s Visualization Nuclear Control Lung adenocarcinoma Cell Marque + RabMAb Portfolio Rabbit Monoclonal Primary Antibodies Coming Soon! BCL6 (EP278) CD19 (EP169) GLUT1 (EP141) Glycophorin A (EP213) IMP3 (EP286) MCM3 (EP202) Myogenin (EP162) Olig2 (EP112) SATB2 (EP281) WT1 (EP122) Also Available BCL2 (E17) c-myc (EP121) Caldesmon (E89) Calponin-1 (EP798Y) CD1a (EP3622) CD4 (EP204) CD5 (EP77) CD14 (EPR3653) CD21 (EP3093) CD99 (EPR3097Y) CD117, c-kit (YR145) CDX-2 (EPR2764Y) Cyclin D1 (EP12) Cytokeratin 5 (EP1601Y) Cytokeratin 10 (EP97) E-cadherin (EP700Y) Estrogen Receptor (EP1) Factor XIIIa (EP3372) GCDFP-15 (EP1582Y) GFAP (EP672Y) Hemoglobin A (EPR3608) Her2/Neu (EP3) MyoD1 (EP212) PAX-5 (EP156) PMS2 (EPR3947) Progesterone Receptor (Y85) PU.1 (EPR3158Y) S100A1 (EP184) Thyroid Peroxidase (EP159) 7

Rev. 0.1 2015 Sigma-Aldrich Co. LLC. All rights reserved. SIGMA-ALDRICH and Cell Marque are trademarks of Sigma-Aldrich Co.