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BMPR2 FISH Probe

The BMPR2 FISH probe is designed to hybridize to the BMPR2 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.

SKU Test Kits Buffer Dye Color Order Now
BMPR2-20-OR  (Standard Design) 20 (40 μL) 200 μL
BMPR2-20-RE 20 (40 μL) 200 μL
BMPR2-20-GO 20 (40 μL) 200 μL
BMPR2-20-GR 20 (40 μL) 200 μL
BMPR2-20-AQ 20 (40 μL) 200 μL
BMPR2-20-DIG 20 (40 μL) 200 μL
BMPR2-20-BIO 20 (40 μL) 200 μL

Gene Summary

This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are BMPs, which are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of two different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. Mutations in this gene have been associated with primary pulmonary hypertension, both familial and fenfluramine-associated, and with pulmonary venoocclusive disease. [provided by RefSeq, Jul 2008]

Gene Details

Gene Symbol: BMPR2

Gene Name: Bone Morphogenetic Protein Receptor Type 2

Chromosome: CHR2: 203241049-203432474

Locus: 2q33.1-q33.2

Gene Diseases

The BMPR2 gene has been associated with the following diseases:

Disease Name
2-Hydroxyglutaricaciduria
49,XXXXX Syndrome
Aagenaes Syndrome
Abderhalden-Kaufmann-Lignac Syndrome
Abrikosov's Tumor
Achard Syndrome
Achard-Thiers Syndrome
Acrocephalopolysyndactyly Type II
Acrokeratoderma, Hereditary Papulotranslucent
Acrootoocular Syndrome
Acrorenal Syndrome
Acrorenal Syndrome Recessive
Adenocarcinoid Tumor
Adrenal Insufficiency, Congenital
Akaba Hayasaka Syndrome
Akesson Syndrome
Aloi Tomasini Isaia Syndrome
Alsing Syndrome
Ameloblastoma
Ameloonychohypohidrotic Syndrome
Androblastoma Of Ovary
Angioedemas, Hereditary
Angiolipomatosis, Familial
Ansell Bywaters Elderking Syndrome
Arakawa Syndrome 2
AREDYLD Syndrome
Arima Syndrome
Asthma
Atrial Septal Defect 4
Atrial Septal Defect 5
Atrial Septal Defect 6
ATRIAL SEPTAL DEFECT 8
ATRIAL SEPTAL DEFECT 9
Aughton Syndrome
Ayazi Syndrome
BADS Syndrome
Baetz-Greenwalt Syndrome
Bagatelle Cassidy Syndrome
Bangstad Syndrome
Bankart Lesions
Banki Syndrome
Banti's Syndrome
Basaran Yilmaz Syndrome
Bassoe Syndrome
Bazopoulou Kyrkanidou Syndrome
Beardwell Syndrome
Beemer Ertbruggen Syndrome
Bellini Chiumello Rimoldi Syndrome
Biemond Syndrome II
Blepharo-cheilo-dontic Syndrome
Blount Disease
Boerhaave Syndrome
Bone Anteversion
Bone Retroversion
Bonneau Syndrome
Boudhina Yedes Khiari Syndrome
Brachioskeletogenital Syndrome
Brachymesomelia Renal Syndrome
Brachymesophalangy 2 And 5
Breast Cancer, Familial
Breast Cancer, Familial Male
Brunoni Syndrome
CAHMR Syndrome
Calabro Syndrome
CAMFAK Syndrome
Campomelia Cumming Type
Cancer
CANOMAD Syndrome
Cantalamessa Baldini Ambrosi Syndrome
Carcinoma
Cardiocranial Syndrome
Carrington Syndrome
CATSHL Syndrome
Cerebrooculonasal Syndrome
Chest Pain
Chilaiditi Syndrome
Chondrosarcoma
CLAPO Syndrome
Cleidorhizomelic Syndrome
Compassion Fatigue
Congenital Absence Of The Sternocleidomastoid Muscle
Corneodermatoosseous Syndrome
Coxoauricular Syndrome
Cranioacrofacial Syndrome
Craniofaciofrontodigital Syndrome
Craniomicromelic Syndrome
Crome Syndrome
Cryofibrinogenemia, Familial Primary
Cryptotia, Familial
Curatolo Cilio Pessagno Syndrome
Daentl Towsend Siegel Syndrome
Daish Hardman Lamont Syndrome
Daneman Davy Mancer Syndrome
Davenport Donlan Syndrome
Death
Degloving Injuries
Dermatoosteolysis Kirghizian Type
Devriendt Syndrome
Dieterich's Disease
Digitorenocerebral Syndrome
Dimauro Disease
Disease
Drachtman Weinblatt Sitarz Syndrome
Dyspnea
Edema
Eye Pain
Faciocardiomelic Syndrome
Faciocardiorenal Syndrome
Fairbank Disease
Familial Dermographism
Familial Hyperbeta- And Prebetalipoproteinemia
Familial Streblodactyly
Fatigue
Fibrosis
FLOTCH Syndrome
Flynn Aird Syndrome
Fountain Syndrome
Fragile X Syndrome
Franceschini Vardeu Guala Syndrome
Freiberg's Disease
Frontoocular Syndrome
Furlong Syndrome
Furukawa Takagi Nakao Syndrome
Gastric Sneezing
Gastrocutaneous Syndrome
Gemignani Syndrome
GEMSS Syndrome
Genoa Syndrome
Giacheti Syndrome
Gigantiform Cementoma, Familial
Glycoprotein Storage Disease
Gollop Coates Syndrome
GOMBO Syndrome
Granddad Syndrome
Grover's Disease
Growth Factors, Combined Defect Of
Grubben De Cock Borghgraef Syndrome
Gurrieri Sammito Bellussi Syndrome
Hadziselimovic Syndrome
Hagemoser Weinstein Bresnick Syndrome
Halal Syndrome
Hamanishi Ueba Tsuji Syndrome
Hamano Tsukamoto Syndrome
Hapnes Boman Skeie Syndrome
Hardikar Syndrome
Heart Failure
Hemoptysis
Hepatic Fibrosis, Congenital
Hereditary Koilonychia
Herrmann Syndrome
Hersh Podruch Weisskopk Syndrome
Hooft Disease
Hordnes Engebretsen Knudtson Syndrome
Human Balantidiasis
Hunt's Syndrome
Hyperexplexia Hereditary
Hyperplasia
Hyperreninemic Hypoaldosteronism, Familial, 2
Hypertension
Hypertrophy
Hypoadrenocorticism, Familial
Hypoglossia, Isolated
Hypoxia
Idiopathic Pulmonary Fibrosis
Iida Kannari Syndrome
IMMUNODEFICIENCY 11
IMMUNODEFICIENCY 12
IMMUNODEFICIENCY 14
IMMUNODEFICIENCY 15
IMMUNODEFICIENCY 16
IMMUNODEFICIENCY 17
IMMUNODEFICIENCY 18
IMMUNODEFICIENCY 19
IMMUNODEFICIENCY 20
IMMUNODEFICIENCY 21
IMMUNODEFICIENCY 22
IMMUNODEFICIENCY 23
IMMUNODEFICIENCY 24
IMMUNODEFICIENCY 28
IMMUNODEFICIENCY 29
IMMUNODEFICIENCY 30
IMMUNODEFICIENCY 36
IMMUNODEFICIENCY 37
IMMUNODEFICIENCY 39
IMMUNODEFICIENCY 40
IMMUNODEFICIENCY 42
IMMUNODEFICIENCY 44
IMMUNODEFICIENCY 45
IMMUNODEFICIENCY 46
IMMUNODEFICIENCY 47
IMMUNODEFICIENCY 48
IMMUNODEFICIENCY 49
IMMUNODEFICIENCY 50
IMMUNODEFICIENCY 51
Infantile Polymyoclonus
Infection
Jagell Holmgren Hofer Syndrome
Kaplowitz Bodurtha Syndrome
Karoshi Death
Kasabach-Merritt Syndrome
Kashani Strom Utley Syndrome
Katsantoni Papadakou Lagoyanni Syndrome
Kennerknecht Sorgo Oberhoffer Syndrome
Kleeblattschaedel Syndrome
Koone Rizzo Elias Syndrome
Kosztolanyi Syndrome
Krasnow Qazi Syndrome
Kuskokwim Disease
Kuzniecky Syndrome
Kyrle Disease
Lachiewicz Sibley Syndrome
Lacrimoauriculodentodigital Syndrome
Lambotte Syndrome
Lelis Syndrome
Lemierre Syndrome
Lyngstadaas Syndrome
Malouf Syndrome
Manouvrier Syndrome
Marchiafava-Bignami Disease
Marsden Syndrome
Massa Casaer Ceulemans Syndrome
Maternal Death
May-Thurner Syndrome
Mehes Syndrome
Melhem Fahl Syndrome
Mengel Konigsmark Syndrome
Meralgia Paraesthetica, Familial
Merlob Grunebaum Reisner Syndrome
Meyenburg-Altherr-Uehlinger Syndrome
Microgastria Limb Reduction Defect
Mirizzi Syndrome
Mollica Pavone Antener Syndrome
MOMES Syndrome
Mononen Karnes Senac Syndrome
Morgellons Disease
Nasodigitoacoustic Syndrome
Nathalie Syndrome
Neuroblastoma
Neurofaciodigitorenal Syndrome
Nevo Syndrome
Nicolau Syndrome
Nievergelt Syndrome
Nivelon Nivelon Mabille Syndrome
Obesity
Oculoauriculofrontonasal Syndrome
Oculocerebrocutaneous Syndrome
Oculodental Syndrome Rutherfurd Syndrome
Oculootoradial Syndrome
Oculopalatocerebral Syndrome
Oculopalatoskeletal Syndrome
Oculorenocerebellar Syndrome
Onat Syndrome
Opticocochleodentate Degeneration
Oroticaciduria 1
Oslam Syndrome
Otoonychoperoneal Syndrome
Pachydermodactyly, Familial
Pain
Paraphilic Disorders
Paraplegia
Parental Death
Pascual Castroviejo Syndrome
Pashayan Syndrome
Passovoy Factor
Pavone Fiumara Rizzo Syndrome
PHACE Association
Pilotto Syndrome
Piriformis Muscle Syndrome
Piussan Lenaerts Mathieu Syndrome
Podder-Tolmie Syndrome
Polythelia, Familial
Postthrombotic Syndrome
Preeyasombat Varavithya Syndrome
Primary Dysautonomias
Propping Zerres Syndrome
Prostate Cancer, Familial
PROSTATE CANCER, HEREDITARY, 1
Prostate Cancer, Hereditary, 12
Prostate Cancer, Hereditary, 13
Prostate Cancer, Hereditary, 6
Prostate Cancer, Hereditary, 8
Pseudoaminopterin Syndrome
Pseudoangiomatous Stromal Hyperplasia
Pseudotrisomy 13 Syndrome
Pulmonary Edema
Pulmonary Edema Of Mountaineers
Pulmonary Fibrosis
Pulmonary Hypertension, Primary, Autosomal Recessive
Pulmonary Veno-Occlusive Disease
Qazi Markouizos Syndrome
Rambaud Galian Syndrome
Ramer Ladda Syndrome
Reginato Schiapachasse Syndrome
Renal Aminoacidurias
Renoprival Hypertension
Retinoblastoma
Retinohepatoendocrinologic Syndrome
RHYNS Syndrome
Ribbing Disease
Richards-Rundle Syndrome
Rombo Syndrome
Rosselli-Gulienetti Syndrome
Rudiger Syndrome
Sakoda Complex
Salcedo Syndrome
Sammartino De Crecchio Syndrome
Sandifer Syndrome
Satoyoshi Syndrome
Schlegelberger Grote Syndrome
Schofer Beetz Bohl Syndrome
Scholte Syndrome
Schrander-Stumpel Theunissen Hulsmans Syndrome
Seaver Cassidy Syndrome
Seemanova Lesny Syndrome
Sener Syndrome
Shapiro Syndrome
Shock
Silengo Lerone Pelizza Syndrome
Sillence Syndrome
Sohval Soffer Syndrome
Spastic Paraplegia 10, Autosomal Dominant
Spastic Paraplegia 11, Autosomal Recessive
Spastic Paraplegia 12, Autosomal Dominant
Spastic Paraplegia 13, Autosomal Dominant
Spastic Paraplegia 14, Autosomal Recessive
Spastic Paraplegia 18, Autosomal Recessive
Spastic Paraplegia 19, Autosomal Dominant
Spastic Paraplegia 20, Autosomal Recessive
Spastic Paraplegia 24
Spastic Paraplegia 24, Autosomal Recessive
Spastic Paraplegia 25, Autosomal Recessive
Spastic Paraplegia 26, Autosomal Recessive
Spastic Paraplegia 27, Autosomal Recessive
Spastic Paraplegia 28, Autosomal Recessive
Spastic Paraplegia 29, Autosomal Dominant
Spastic Paraplegia 3, Autosomal Dominant
Spastic Paraplegia 30, Autosomal Recessive
Spastic Paraplegia 31, Autosomal Dominant
Spastic Paraplegia 32, Autosomal Recessive
Spastic Paraplegia 33, Autosomal Dominant
SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE
Spastic Paraplegia 36, Autosomal Dominant
Spastic Paraplegia 37, Autosomal Dominant
Spastic Paraplegia 38, Autosomal Dominant
Spastic Paraplegia 39, Autosomal Recessive
Spastic Paraplegia 4, Autosomal Dominant
SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT
Spastic Paraplegia 42, Autosomal Dominant
SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE
Spastic Paraplegia 44, Autosomal Recessive
SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE
Spastic Paraplegia 6, Autosomal Dominant
Spastic Paraplegia 7, Autosomal Recessive
Spastic Paraplegia 9, Autosomal Dominant
Spastic Paraplegia Type 7
Spastic Paraplegia Type 8
Spastic Paraplegia-50, Autosomal Recessive
Spastic Pseudosclerosis
Starvation
Steinfeld Syndrome
Sulfhemoglobinemia, Congenital
Summitt Syndrome
SUNCT Syndrome
Susac Syndrome
Syncope
Syndrome
Tabatznik Syndrome
Three M Syndrome 2
Thyroid Hormone Metabolism, Abnormal
Tonoki Syndrome
Trichodental Syndrome
Triglyceride Storage Disease, Type I
Triglyceride Storage Disease, Type II
Triple X Syndrome
Trueb Burg Bottani Syndrome
Tsukahara Syndrome
Tucker Syndrome
Twinning Due To Superfetation
Upington Disease
Uterine Retroversion
Vascular Remodeling
Velofacioskeletal Syndrome
Verloove-Vanhorick Brubakk Syndrome
Volcke Soekarman Syndrome
Walbaum Titran Durieux Crepin Syndrome
Waldmann Disease
Warburton Anyane Yeboa Syndrome
Warman Mulliken Hayward Syndrome
Weismann Netter Syndrome
WT Limb Blood Syndrome
Wyburn Mason's Syndrome
Yusho Disease
Zazam Sheriff Phillips Syndrome
Zechi-Ceide Syndrome
Zlotogora-Ogur Syndrome
Zuska's Disease

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Scientific Citations

There are currently no FISH related citations for this gene.

Product Details

Product: BMPR2 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: BMPR2-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping