Clear Filter
  • (32)
  • (7)
  • (14)
  • (14)
  • (2)
  • (2)
  • (16)
  • (12)
  • (2)
  • (29)
  • (3)
  • (23)
  • (9)
  • (21)
  • (3)
  • (1)
  • (21)
  • (4)
  • (2)
  • (27)
  • (5)
  • (1)
  • (7)
  • (12)
  • (10)
  • (2)
  • (26)
  • (4)
  • (2)
  • (2)
  • (2)
  • (1)
  • (32)
  • (31)
  • (1)
  Clear Filter

Search Results for - "MTHFR"

Remove Quotes
 (and perform a Special Operators or a general search)
 Use filters to refine search | Additional fields available - click "Fields" button
Loading ...
1 - 32 of 32 Results
Selected Items: 0
Page Size:
 
 
Quick View
 
ID
 
Description
 
Product
 
Source
(Showing Items: 32)
 
 
 
 
HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
LCL
 
B-Lymphocyte
 
 
 
 
5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
 
DNA
 
LCL
 
 
 
 
5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
 
DNA
 
LCL
 
 
 
 
5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY | HUMAN GENE MUTATION PANEL - DISORDERS OF THROMBOSIS
 
DNA
 
LCL
 
 
 
 
5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
DNA
 
LCL
 
 
 
 
HEMOPHILIA B; HEMB | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
DNA
 
LCL
 
 
 
 
5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | FACTOR V DEFICIENCY
 
DNA
 
LCL
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL | HEMOCHROMATOSIS; HFE | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS
 
DNA
 
LCL
 
 
 
 
5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | FACTOR V DEFICIENCY
 
LCL
 
B-Lymphocyte
 
 
 
 
5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
LCL
 
B-Lymphocyte
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL | HEMOCHROMATOSIS; HFE | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS
 
LCL
 
B-Lymphocyte
 
 
 
 
HEMOPHILIA B; HEMB | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
LCL
 
B-Lymphocyte
 
 
 
 
DYSTROPHIA MYOTONICA 1; DM1 | DYSTROPHIA MYOTONICA PROTEIN KINASE; DMPK | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
LCL
 
B-Lymphocyte
 
 
 
 
DYSTROPHIA MYOTONICA 1; DM1 | DYSTROPHIA MYOTONICA PROTEIN KINASE; DMPK | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
High Molecular Weight DNA
 
B-Lymphocyte
 
 
 
 
HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
 
Fibroblast
 
 
 
 
 
HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
 
LCL
 
B-Lymphocyte
 
 
 
 
HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
 
DNA
 
Fibroblast
 
 
 
 
HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
 
LCL
 
B-Lymphocyte
 
 
 
 
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1; CADASIL1 | NOTCH, DROSOPHILA, HOMOLOG OF, 3; NOTCH3 | HYPERHOMOCYSTEINEMIA | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
LCL
 
B-Lymphocyte
 
 
 
 
DYSTROPHIA MYOTONICA 1; DM1 | DYSTROPHIA MYOTONICA PROTEIN KINASE; DMPK | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
DNA
 
LCL
 
 
 
 
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1; CADASIL1 | NOTCH, DROSOPHILA, HOMOLOG OF, 3; NOTCH3 | HYPERHOMOCYSTEINEMIA | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
 
Fibroblast
 
 
 
 
 
COAGULATION FACTOR II; F2 | HEMOCHROMATOSIS; HFE | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HUMAN GENE MUTATION PANEL - DISORDERS OF THROMBOSIS | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS | HOMEOSTATIC IRON REGULATOR; HFE
 
DNA
 
LCL
 
 
 
 
CYSTIC FIBROSIS; CF | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HUMAN GENE MUTATION PANEL - CYSTIC FIBROSIS (VERSION 2)
 
DNA
 
LCL
 
 
 
 
CYSTIC FIBROSIS; CF | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HUMAN GENE MUTATION PANEL - CYSTIC FIBROSIS (VERSION 2)
 
LCL
 
B-Lymphocyte
 
 
 
 
CYSTIC FIBROSIS; CF | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR | HEMOCHROMATOSIS; HFE | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS | HUMAN GENE MUTATION PANEL - CYSTIC FIBROSIS (VERSION 2) | HOMEOSTATIC IRON REGULATOR; HFE
 
DNA
 
LCL
 
 
 
 
CYSTIC FIBROSIS; CF | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR | HEMOCHROMATOSIS; HFE | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS | HUMAN GENE MUTATION PANEL - CYSTIC FIBROSIS (VERSION 2) | HOMEOSTATIC IRON REGULATOR; HFE
 
High Molecular Weight DNA
 
B-Lymphocyte
 
 
 
 
COAGULATION FACTOR II; F2 | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | FACTOR V DEFICIENCY | HEMOCHROMATOSIS; HFE | HUMAN GENE MUTATION PANEL - DISORDERS OF THROMBOSIS | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS
 
DNA
 
LCL
 
 
 
 
CYSTIC FIBROSIS; CF | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR | HEMOCHROMATOSIS; HFE | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS | HUMAN GENE MUTATION PANEL - CYSTIC FIBROSIS (VERSION 2) | HOMEOSTATIC IRON REGULATOR; HFE
 
LCL
 
B-Lymphocyte
 
 
 
 
COAGULATION FACTOR II; F2 | HEMOCHROMATOSIS; HFE | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | HUMAN GENE MUTATION PANEL - DISORDERS OF THROMBOSIS | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS | HOMEOSTATIC IRON REGULATOR; HFE
 
LCL
 
B-Lymphocyte
 
 
 
 
DYSTROPHIA MYOTONICA 1; DM1
 
DNA
 
Fibroblast
 
 
 
 
COAGULATION FACTOR II; F2 | 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | FACTOR V DEFICIENCY | HEMOCHROMATOSIS; HFE | HUMAN GENE MUTATION PANEL - DISORDERS OF THROMBOSIS | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS
 
LCL
 
B-Lymphocyte
 
 
 
 
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1; CADASIL1 | NOTCH, DROSOPHILA, HOMOLOG OF, 3; NOTCH3
 
LCL
 
B-Lymphocyte

No Results were Found

1 - 32 of 32 Results
Selected Items: 0
Page Size:

CORIELL RESEARCH SERVICES



Apart from our online Catalog, Coriell also offers the greater scientific community a wide range of laboratory services. Our custom services include iPSC services, R&D services, assay development, custom lab services, genomic services, bioinformatic analysis, etc., to name a few. 


Learn More 
(Open in New Tab)
Footer

Our mission is to prevent and cure disease through biomedical research.

CONTACT US

CUSTOMER SERVICE
customerservice@coriell.org (800) 752-3805 ● (856) 757-4848
Subscribe to our newsletter here

Coriell Institute for Medical Research
403 Haddon Avenue Camden, NJ 08103, USA (856) 966-7377

Ⓒ 2025 Coriell Institute. All rights reserved.