ScopeUniversitätsklinikum Ulm Diagnostische Laboratorien der Universitätsklinik für Kinder- und Jugendmedizin Ulm
189 capabilities
Accredited since May 2025
Verified May 2026
One of 3,188 in Germany
Send one structured enquiry and we chase the reply for you. No cold email, no chasing.
Details
Eythstr. 24
Ulm 89075 , Germany
Ulm 89075 , Germany
Accreditation
Active
DAkkS
D-ML-13294-08-00
Offers clinical chemistry, immunology, and molecular human genetics testing with accreditation flexibility for free selection of standardised procedures and development of new analytical methods.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13294-08-00
Status
ActiveSince
13 May 2025
Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.
Download Scope PDF
Test Capabilities (189)
| Standard Reference | Description | Category |
|---|---|---|
| (CD4/25/FoxP3+) | (CD4/25/FoxP3+) | Biological / Microbiological |
| (NK- und CTL Funktionstest) | (NK- und CTL Funktionstest) | Biological / Microbiological |
| B-Zell Phänotypisierung | B-Zell Phänotypisierung | Biological / Microbiological |
| CD107a Release Assay | CD107a Release Assay | Biological / Microbiological |
| CD25-Mangel | CD25-Mangel | Biological / Microbiological |
| CD40 | CD40 | Biological / Microbiological |
| CD40L | CD40L | Biological / Microbiological |
| CD95 (Fas, Apo1) | CD95 (Fas, Apo1) | Biological / Microbiological |
| Granulozyten Burst | Granulozyten Burst | Biological / Microbiological |
| Granulozyten Phagozytose | Granulozyten Phagozytose | Biological / Microbiological |
| HLA-Chimärismus Analyse | HLA-Chimärismus Analyse | Biological / Microbiological |
| IFNgR (CD119) Analyse | IFNgR (CD119) Analyse | Biological / Microbiological |
| IL2RA, Schwerer kombinierter | IL2RA, Schwerer kombinierter | Biological / Microbiological |
| IL2RG, schwerer kombinierter | IL2RG, schwerer kombinierter | Biological / Microbiological |
| Immundefekt (X-SCID ) | Immundefekt (X-SCID ) | Biological / Microbiological |
| Immundefekt Immundefekt | Immundefekt Immundefekt | Biological / Microbiological |
| Intrazelluläre Zytokine (IL17, IFNg) | Intrazelluläre Zytokine (IL17, IFNg) | Biological / Microbiological |
| JAK3, Schwerer kombinierter | JAK3, Schwerer kombinierter | Biological / Microbiological |
| Perforin Analyse | Perforin Analyse | Biological / Microbiological |
| RTE (recent thymic emigrants) | RTE (recent thymic emigrants) | Biological / Microbiological |
| T-Zell Funktions Analyse | T-Zell Funktions Analyse | Biological / Microbiological |
| T-Zell Rezeptor Analyse | T-Zell Rezeptor Analyse | Biological / Microbiological |
| Urinbestandteile | Urinbestandteile | Biological / Microbiological |
| Wiscott Aldrich Syndrome | Wiscott Aldrich Syndrome | Biological / Microbiological |
| XIAP_SAP_NK T Analyse | XIAP_SAP_NK T Analyse | Biological / Microbiological |
| Aminosäurendiagnostik | Aminosäurendiagnostik | Chromatography (GC, HPLC) |
| verschiedene Aminosäuren) | verschiedene Aminosäuren) | Chromatography (GC, HPLC) |
| Zellzählung | Zellzählung | Clinical Chemistry |
| & gutartige familiäre Chorea | & gutartige familiäre Chorea | Elemental Analysis |
| (HH; HFE1) | (HH; HFE1) | Elemental Analysis |
| 2-Hydroxyglutarat (2HG), 2-hydroxyglutaric aciduria | 2-Hydroxyglutarat (2HG), 2-hydroxyglutaric aciduria | Elemental Analysis |
| Darmerkrankung, Interleukin | Darmerkrankung, Interleukin | Elemental Analysis |
| G6PC1; Glykogen-Speicherkrankheit | G6PC1; Glykogen-Speicherkrankheit | Elemental Analysis |
| GCK, Maturity-Onset Diabetes | GCK, Maturity-Onset Diabetes | Elemental Analysis |
| Gigantismus | Gigantismus | Elemental Analysis |
| Granulomatose; neutrophiler | Granulomatose; neutrophiler | Elemental Analysis |
| HAMP, Hereditäre | HAMP, Hereditäre | Elemental Analysis |
| HFE, Hereditäre Hämochromatose | HFE, Hereditäre Hämochromatose | Elemental Analysis |
| HFE-Polymorphismen, Hereditäre | HFE-Polymorphismen, Hereditäre | Elemental Analysis |
| HNF1A/TCF1, Maturity-Onset | HNF1A/TCF1, Maturity-Onset | Elemental Analysis |
| HNF4A, Maturity-Onset | HNF4A, Maturity-Onset | Elemental Analysis |
| HVJ, Hämochromatose Typ2A | HVJ, Hämochromatose Typ2A | Elemental Analysis |
| Hämochromatose | TRF2/HFE3, Hämochromatose | Elemental Analysis |
| Hämochromatose, juvenile | Hämochromatose, juvenile | Elemental Analysis |
| Hämojuvelin (HFE2) | Hämojuvelin (HFE2) | Elemental Analysis |
| IDH1, lösliche | IDH1, lösliche | Elemental Analysis |
| IDH2, mitochondriale | IDH2, mitochondriale | Elemental Analysis |
| IL10, Entzündliche | IL10, Entzündliche | Elemental Analysis |
| IL10RA, Entzündliche | IL10RA, Entzündliche | Elemental Analysis |
| IL10RB, Entzündliche | IL10RB, Entzündliche | Elemental Analysis |
| Isocitratdehydrogenase | Isocitratdehydrogenase | Elemental Analysis |
| KCNN4 Dehydrierte hereditäre | KCNN4 Dehydrierte hereditäre | Elemental Analysis |
| KLF1, kongenitale | KLF1, kongenitale | Elemental Analysis |
| LEP, Adipositas, Ess-Sucht | LEP, Adipositas, Ess-Sucht | Elemental Analysis |
| Lipodystrophie mit | Lipodystrophie mit | Elemental Analysis |
| MC4R, Adipositas, Ess-Sucht | MC4R, Adipositas, Ess-Sucht | Elemental Analysis |
| NCF2, CGD; Chronic | NCF2, CGD; Chronic | Elemental Analysis |
| NEUROG3, Diarrhoe, kongenitale | NEUROG3, Diarrhoe, kongenitale | Elemental Analysis |
| NKX2-1, kongenitale Hypothyreose | NKX2-1, kongenitale Hypothyreose | Elemental Analysis |
| NSD1, Sotos-Syndrom, Cerebraler | NSD1, Sotos-Syndrom, Cerebraler | Elemental Analysis |
| PIEZO1 Dehydrierte hereditäre | PIEZO1 Dehydrierte hereditäre | Elemental Analysis |
| PTRF, kongenitale, generalisierte | PTRF, kongenitale, generalisierte | Elemental Analysis |
| autosomal-dominantes | autosomal-dominantes | Elemental Analysis |
| dyserythropoietische Anämie, IV (CDA IV) | dyserythropoietische Anämie, IV (CDA IV) | Elemental Analysis |
| lipatrophischerDiabetes | lipatrophischerDiabetes | Elemental Analysis |
| malabsorptive, durch Mangel | malabsorptive, durch Mangel | Elemental Analysis |
| the Young, MODY-Diabetes, Typ 2 | the Young, MODY-Diabetes, Typ 2 | Elemental Analysis |
| the Young, MODY-Diabetes, Typ1 (MODY1) | the Young, MODY-Diabetes, Typ1 (MODY1) | Elemental Analysis |
| -Differenzierung | Zelldifferenzierung | Hematology |
| Differenzialblutbild | Differenzialblutbild | Hematology |
| (WASP) | (WASP) | Immunology / Serology |
| CD34+ Stammzellen | CD34+ Stammzellen | Immunology / Serology |
| Interleukin 10 | Interleukin 10 | Immunology / Serology |
| Leukozytenadhäsionsmoleküle | Leukozytenadhäsionsmoleküle | Immunology / Serology |
| Lymphozytenphänotypisierung | Lymphozytenphänotypisierung | Immunology / Serology |
| Regulatorische T-Zellen | Regulatorische T-Zellen | Immunology / Serology |
| (ALPS1a), Canale-Smith-Syndrom | (ALPS1a), Canale-Smith-Syndrom | Molecular Diagnostics / PCR |
| (ALPS1b), Canale-Smith-Syndrom | (ALPS1b), Canale-Smith-Syndrom | Molecular Diagnostics / PCR |
| (ALPS2a), Canale-Smith-Syndrom | (ALPS2a), Canale-Smith-Syndrom | Molecular Diagnostics / PCR |
| (ALPS2b), Canale-Smith-Syndrom | (ALPS2b), Canale-Smith-Syndrom | Molecular Diagnostics / PCR |
| (ALPS4); N-RAS Exon 2 | (ALPS4); N-RAS Exon 2 | Molecular Diagnostics / PCR |
| (APS1), APECED | (APS1), APECED | Molecular Diagnostics / PCR |
| (DBA) | (DBA) | Molecular Diagnostics / PCR |
| (DBA5) | (DBA5) | Molecular Diagnostics / PCR |
| (FDAMI) | (FDAMI) | Molecular Diagnostics / PCR |
| (IBD1), Morbus Crohn & | (IBD1), Morbus Crohn & | Molecular Diagnostics / PCR |
| (VOD), p.P268S, p.R702W,p.G908R, p.L1007Pfs | (VOD), p.P268S, p.R702W,p.G908R, p.L1007Pfs | Molecular Diagnostics / PCR |
| (XLP), Purtillo-Syndrom | (XLP), Purtillo-Syndrom | Molecular Diagnostics / PCR |
| (familiaeres), FMF | (familiaeres), FMF | Molecular Diagnostics / PCR |
| 401C/T (rs3758149) | 401C/T (rs3758149) | Molecular Diagnostics / PCR |
| Alpha Kette - CYBA | Alpha Kette - CYBA | Molecular Diagnostics / PCR |
| Anämie mit hepatischer | Anämie mit hepatischer | Molecular Diagnostics / PCR |
| Ausscheidung- hohe MTX-Spiegel | Ausscheidung- hohe MTX-Spiegel | Molecular Diagnostics / PCR |
| Autoimmunkrankheit ad | Autoimmunkrankheit ad | Molecular Diagnostics / PCR |
| CD3D, Schwerer kombinierter | CD3D, Schwerer kombinierter | Molecular Diagnostics / PCR |
| CD3D-Defekt | CD3D-Defekt | Molecular Diagnostics / PCR |
| CD3DE Schwerer kombinierter | CD3DE Schwerer kombinierter | Molecular Diagnostics / PCR |
| CD3E-Defekt | CD3E-Defekt | Molecular Diagnostics / PCR |
| CD40, Immundefizienz mit | CD40, Immundefizienz mit | Molecular Diagnostics / PCR |
| CLCN7, Osteopetrose, infantil | CLCN7, Osteopetrose, infantil | Molecular Diagnostics / PCR |
| CTLA4, T-Zellfunktionsverlust | CTLA4, T-Zellfunktionsverlust | Molecular Diagnostics / PCR |
| CYBA, CGD; Chronic | CYBA, CGD; Chronic | Molecular Diagnostics / PCR |
| CYBB, CGD1; chronic | CYBB, CGD1; chronic | Molecular Diagnostics / PCR |
| Diabetes, MODY Typ 3 | Diabetes, MODY Typ 3 | Molecular Diagnostics / PCR |
| Disease | granulomatous disease | Molecular Diagnostics / PCR |
| Dysplasie. X-chromosomal | Dysplasie. X-chromosomal | Molecular Diagnostics / PCR |
| Dystrophin-Gen, Muskeldystrophie | Dystrophin-Gen, Muskeldystrophie | Molecular Diagnostics / PCR |
| Eisenüberladung | Eisenüberladung | Molecular Diagnostics / PCR |
| Ektodermale Dysplasie Typ | Ektodermale Dysplasie Typ | Molecular Diagnostics / PCR |
| Familiäre partielle Lipodystrophie | Familiäre partielle Lipodystrophie | Molecular Diagnostics / PCR |
| GATA1, Anaemie, dyserythropoetische mit | GATA1, Anaemie, dyserythropoetische mit | Molecular Diagnostics / PCR |
| GGH-Promotor, Störung | GGH-Promotor, Störung | Molecular Diagnostics / PCR |
| Gilbert-Syndrom | Gilbert-Syndrom | Molecular Diagnostics / PCR |
| Granulomatose; Cytochrome | Granulomatose; Cytochrome | Molecular Diagnostics / PCR |
| Hereditäre Xerozytose | Hereditäre Xerozytose | Molecular Diagnostics / PCR |
| Hypogammaglobulinämie | Hypogammaglobulinämie | Molecular Diagnostics / PCR |
| Hämochromatose Typ 4 | Hämochromatose Typ 4 | Molecular Diagnostics / PCR |
| IFNGR1, Familiaere disseminierte | IFNGR1, Familiaere disseminierte | Molecular Diagnostics / PCR |
| IL7R, Schwerer kombinierter | IL7R, Schwerer kombinierter | Molecular Diagnostics / PCR |
| IL7R-Defekt | IL7R-Defekt | Molecular Diagnostics / PCR |
| ITK, Lymphoproliferative | ITK, Lymphoproliferative | Molecular Diagnostics / PCR |
| IgM-Syndrom, HIGM 3 | IgM-Syndrom, HIGM 3 | Molecular Diagnostics / PCR |
| Immundysregulation, Polyendokrinopathie und | Immundysregulation, Polyendokrinopathie und | Molecular Diagnostics / PCR |
| Inflammatory Bowel Disease | Inflammatory Bowel Disease | Molecular Diagnostics / PCR |
| Lymphoproliferatives Syndrom | lymphoproliferatives Syndrom | Molecular Diagnostics / PCR |
| MBL2, Opsonisierungs Defekt, Mannonse-Bindung Lektin-2 | MBL2, Opsonisierungs Defekt, Mannonse-Bindung Lektin-2 | Molecular Diagnostics / PCR |
| MEFV, Mittelmeerfieber | MEFV, Mittelmeerfieber | Molecular Diagnostics / PCR |
| MPL, kongenitale | MPL, kongenitale | Molecular Diagnostics / PCR |
| Mangel; Polymorphismen | Mangel; Polymorphismen | Molecular Diagnostics / PCR |
| OSTM1, Osteopetrose, infantil | OSTM1, Osteopetrose, infantil | Molecular Diagnostics / PCR |
| PRF1, Familiaere | PRF1, Familiaere | Molecular Diagnostics / PCR |
| Periodisches Fieber, FPF | Periodisches Fieber, FPF | Molecular Diagnostics / PCR |
| Polymorphismen im Exon | Polymorphismen im Exon | Molecular Diagnostics / PCR |
| Promotor und Exon 1: -550 | Promotor und Exon 1: -550 | Molecular Diagnostics / PCR |
| RANK, Osteopetrose, (TNFRSF11) | RANK, Osteopetrose, (TNFRSF11) | Molecular Diagnostics / PCR |
| RANKL, Osteopetrose, Osteoklasten-Mangel (TNFSF11) | RANKL, Osteopetrose, Osteoklasten-Mangel (TNFSF11) | Molecular Diagnostics / PCR |
| RPL5, Diamond-Blackfan | RPL5, Diamond-Blackfan | Molecular Diagnostics / PCR |
| RPS19, Diamond-Blackfan | RPS19, Diamond-Blackfan | Molecular Diagnostics / PCR |
| Rezeptor, alpha; IL10RA | Rezeptor, alpha; IL10RA | Molecular Diagnostics / PCR |
| Rezeptor, alpha; IL10RB | Rezeptor, alpha; IL10RB | Molecular Diagnostics / PCR |
| SH2D1A, SAP, X-chromosomales | SH2D1A, SAP, X-chromosomales | Molecular Diagnostics / PCR |
| SLC11A2/DMT1, Mikrozytische | SLC11A2/DMT1, Mikrozytische | Molecular Diagnostics / PCR |
| SLC19A2, Thiamin-responsives | SLC19A2, Thiamin-responsives | Molecular Diagnostics / PCR |
| SNX10, Osteopetrose, infantil | SNX10, Osteopetrose, infantil | Molecular Diagnostics / PCR |
| Syndrom (TRMA) | Syndrom (TRMA) | Molecular Diagnostics / PCR |
| T2DM; Hyperproinsulinaemie | T2DM; Hyperproinsulinaemie | Molecular Diagnostics / PCR |
| TCIRG1, Osteopetrose, infantil | TCIRG1, Osteopetrose, infantil | Molecular Diagnostics / PCR |
| THPO, Familiäre | THPO, Familiäre | Molecular Diagnostics / PCR |
| TMPRSS6, hereditäre | TMPRSS6, hereditäre | Molecular Diagnostics / PCR |
| TNFRSF1A, TRAPS, Familiaeres | TNFRSF1A, TRAPS, Familiaeres | Molecular Diagnostics / PCR |
| TREX1, Aicardi-Goutieres | TREX1, Aicardi-Goutieres | Molecular Diagnostics / PCR |
| Thrombozytose/ Thrombozythämie | Thrombozytose/ Thrombozythämie | Molecular Diagnostics / PCR |
| Thrombozytose/Thrombpzythämie | Thrombozytose/Thrombpzythämie | Molecular Diagnostics / PCR |
| WAS, Wiskott-Aldrich Syndrom | WAS, Wiskott-Aldrich Syndrom | Molecular Diagnostics / PCR |
| X-chromosomales Syndrom | X-chromosomales Syndrom | Molecular Diagnostics / PCR |
| XIAP, BIRC4, X-chromosomales | XIAP, BIRC4, X-chromosomales | Molecular Diagnostics / PCR |
| ZAP70, Schwerer kombinierter | ZAP70, Schwerer kombinierter | Molecular Diagnostics / PCR |
| [HIGS; AD-HIES (LOF)] und | [HIGS; AD-HIES (LOF)] und | Molecular Diagnostics / PCR |
| abhängige Epilepsie (EPD) | abhängige Epilepsie (EPD) | Molecular Diagnostics / PCR |
| amegakaryozytäre | amegakaryozytäre | Molecular Diagnostics / PCR |
| assoz. früh beginnende | assoz. früh beginnende | Molecular Diagnostics / PCR |
| atypische Mycobakterielle | atypische Mycobakterielle | Molecular Diagnostics / PCR |
| autosmal-rezessive; IL2-inducible | autosmal-rezessive; IL2-inducible | Molecular Diagnostics / PCR |
| cell kinase | cell kinase | Molecular Diagnostics / PCR |
| chromosomales, HIGM 1 | chromosomales, HIGM 1 | Molecular Diagnostics / PCR |
| cytochrome b-245, beta | cytochrome b-245, beta | Molecular Diagnostics / PCR |
| exonuclease 1; DNASe III | exonuclease 1; DNASe III | Molecular Diagnostics / PCR |
| generalisierte kongenitale | generalisierte kongenitale | Molecular Diagnostics / PCR |
| haemophagozytierende | haemophagozytierende | Molecular Diagnostics / PCR |
| maligne | maligne | Molecular Diagnostics / PCR |
| maligne & autosomal dominant | maligne & autosomal dominant | Molecular Diagnostics / PCR |
| megaloblastisches Anämie | megaloblastisches Anämie | Molecular Diagnostics / PCR |
| multisystemische | multisystemische | Molecular Diagnostics / PCR |
| p.H63D, p.S65C und p.C282Y | p.H63D, p.S65C und p.C282Y | Molecular Diagnostics / PCR |
| p.R201C, p.R201H, p.R201G, p.Q227H, p.Q227R | p.R201C, p.R201H, p.R201G, p.Q227H, p.Q227R | Molecular Diagnostics / PCR |
| sekundären Glioblastomen | sekundären Glioblastomen | Molecular Diagnostics / PCR |
| therapieresistente | therapieresistente | Molecular Diagnostics / PCR |
| (ADOII, Albers-Schoenberg | (ADOII, Albers-Schoenberg | Other |
| (angeborener Leptin-Mangel | (angeborener Leptin-Mangel | Other |
| B-) | a), b) | Other |
| Eisenmangelanämie (engl. | Eisenmangelanämie (engl. | Other |
| IRIDA) | IRIDA) | Other |
| Immundefekt (SCID, T- B+ | Immundefekt (SCID, T- B+ | Other |
| Immundefekt (SCID, T-, Defekt, CD8-Mangel | Immundefekt (SCID, T-, Defekt, CD8-Mangel | Other |
| Immundefekt (SCID, T-, JAK3-Defekt | Immundefekt (SCID, T-, JAK3-Defekt | Other |
| carrier family 40 (iron-regulated | carrier family 40 (iron-regulated | Other |
| chromosomal) | chromosomal) | Other |
| transporter), member 1, SLC40A1 | transporter), member 1, SLC40A1 | Other |
| TPA (Tissue Polypeptide | TPA (Tissue Polypeptide | Spectroscopy (XRF, ICP, AAS) |
Send an Enquiry
Request a quote, ask about capacity, or discuss your testing requirements directly with this lab.