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Search Results for - "LMNA"

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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
MONO-ALLELIC mGFP-TAGGED LMNB1 CONTAINING LMNA-G608G (TAG AT N-TERM) | Laminopathy Disease Collection AICS-0119
 
Collection of iPSC
 
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED | LAMIN A/C; LMNA
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
Fibroblast
 
Skin, Skin
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
Fibroblast
 
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
Fibroblast
 
Skin, Skin
 
 
 
 
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT; EDMD2 | LAMIN A/C; LMNA
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
DNA
 
Fibroblast
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
DNA
 
Fibroblast
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
DNA
 
Fibroblast
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED | LAMIN A/C; LMNA
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
DNA
 
Fibroblast
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
DNA
 
Fibroblast
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
Fibroblast
 
Skin, Thigh
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
Fibroblast
 
Skin, Leg
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
Fibroblast
 
Skin, Arm
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
Fibroblast
 
Skin, Thigh
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
iPSC
 
Fibroblast
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
Fibroblast
 
Skin, Thorax
 
 
 
 
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT; EDMD2 | LAMIN A/C; LMNA
 
DNA
 
LCL
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED | LAMIN A/C; LMNA
 
DNA
 
LCL
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
DNA
 
Fibroblast
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED | LAMIN A/C; LMNA
 
DNA
 
LCL
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
DNA
 
LCL
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
iPSC
 
Fibroblast
 
 
 
 
SEIP SYNDROME | LAMIN A/C; LMNA
 
Fibroblast
 
Skin, Skin
 
 
 
 
MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
LCL
 
B-Lymphocyte
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED | LAMIN A/C; LMNA
 
LCL
 
B-Lymphocyte
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED | LAMIN A/C; LMNA
 
LCL
 
B-Lymphocyte
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
DNA
 
LCL
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED | LAMIN A/C; LMNA
 
DNA
 
LCL
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
DNA
 
LCL
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
DNA
 
LCL
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
DNA
 
LCL
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
DNA
 
LCL
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
Fibroblast
 
Skin, Skin
 
 
 
 
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT; EDMD2
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
DNA
 
Fibroblast
 
 
 
 
MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
DNA
 
LCL
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | LAMIN A/C; LMNA
 
Fibroblast
 
Skin, Arm
 
 
 
 
HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS
 
iPSC
 
Fibroblast
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED | LAMIN A/C; LMNA | NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
 
DNA
 
Fibroblast
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED | LAMIN A/C; LMNA | IPSC
 
iPSC
 
Fibroblast
 
 
 
 
MENTAL RETARDATION, X-LINKED 106; MRX106 | O-LINKED N-ACETYLGLUCOSAMINE TRANSFERASE; OGT
 
LCL
 
B-Lymphocyte
 
 
 
 
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT; EDMD2
 
DNA
 
Fibroblast

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