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Stem Cells

 

Stem Cells, also calls Progenitor Cells, are a kind of self-replicating pluripotent cells, which can differentiate into multiple functional cells under certain conditions. Given this characteristic, some diseases can be cured by transplanting stem cells or related derivatives into patients to replace damaged cells. Stem cells have become the frontier and hotspot of life science and medical research at the beginning of this century because of the broad application prospects in the fields of disease treatment and regenerative medicine.

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ABC-SC2075

HighQC™ Human IPSC From Fibroblast-Familial Alzheimer’s Disease

Cell Type: iPSC; Primary Tissue: Fibroblast; Reprogramming Method: Episomal Plasmid; Disease: Famili...more +inquiry

ABC-SC2073

HighQC™ Human IPSC From PBMC-ALS

Cell Type: iPSC; Primary Tissue: PBMC; Disease: Amyotrophic Lateral Sclerosis(ALS); Cells are only g...more +inquiry

ABC-SC2072

HighQC™ Human IPSC From Fibroblast-Monocarboxylate Transporter 9-Specific Thyroid Hormone Cell Transporter Deficiency

Cell Type: iPSC; Primary Tissue: Fibroblast; Reprogramming Method: Episomal Plasmid; Disease: Monoca...more +inquiry

ABC-SC2071

HighQC™ Human IPSC From Fibroblast-Monocarboxylate Transporter 8-Specific Thyroid Hormone Cell Transporter Deficiency

Cell Type: iPSC; Primary Tissue: Fibroblast; Reprogramming Method: Episomal Plasmid; Disease: Monoca...more +inquiry

ABC-SC2070

HighQC™ Human IPSC From PBMC-Control

Cell Type: iPSC; Primary Tissue: PBMC Reprogramming Method: Episomal Plasmid; Disease: Control; Cell...more +inquiry

ABC-SC2069

HighQC™ Human IPSC From B-Lymphocyte-Apparently Healthy Individual

Apparently Healthy Individual; Subcollection: Apparently healthy iPSCs Apparently Healthy Collection...more +inquiry

ABC-SC2068

HighQC™ Human IPSC From B-Lymphocyte-Ceroid Lipofuscinosis(Neuronal 2-Late Infantile Type)

Ceroid Lipofuscinosis(Neuronal 2-Late Infantile Type); CLN2 CLN2 GENE; CLN2; Subcollection: Heritabl...more +inquiry

ABC-SC2066

HighQC™ Human IPSC From Fibroblast-Phenylketonuria

Phenylketonuria; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed with pu...more +inquiry

ABC-SC2065

HighQC™ Human IPSC From Fibroblast-Hutchinson-Gilford Progeria Syndrome

Hutchinson-Gilford Progeria Syndrome; HGPS; Subcollection: Heritable Diseases; Affected: YES; Cells ...more +inquiry

ABC-SC2064

HighQC™ Human IPSC From Fibroblast-Congenital Disorder Of Deglycosylation

Congenital Disorder Of Deglycosylation; CDDG N-GLYCANASE 1; NGLY1 MALIGNANT HYPERTHERMIA SUSCEPTIBIL...more +inquiry

ABC-SC2063

HighQC™ Human IPSC From Fibroblast-Wolman Disease

Wolman Disease; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed with pur...more +inquiry

ABC-SC2062

HighQC™ Human IPSC From Fibroblast-Pitt-Hopkins Syndrome

Pitt-Hopkins Syndrome; PTHS TRANSCRIPTION FACTOR 4; TCF4; Subcollection: Heritable Diseases PIGI Con...more +inquiry

ABC-SC2059

HighQC™ Human IPSC From Fibroblast-Werner Syndrome

Werner Syndrome; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED LAMIN A/C; LMNA ...more +inquiry

ABC-SC2058

HighQC™ Human IPSC From Fibroblast-Choroideremia

Choroideremia; CHM CHM GENE; CHM; Subcollection: Heritable Diseases PIGI Consented Sample; Affected:...more +inquiry

ABC-SC2057

HighQC™ Human IPSC From Fibroblast-Lesch-Nyhan Syndrome

Lesch-Nyhan Syndrome; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT; Subcollecti...more +inquiry

ABC-SC2056

HighQC™ Human IPSC From Fibroblast-Huntington Disease

Huntington Disease; HD; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed ...more +inquiry

ABC-SC2055

HighQC™ Human IPSC From Fibroblast-Tuberous Sclerosis 2

Tuberous Sclerosis 2; TSC2 TSC2 GENE; TSC2; Subcollection: Heritable Diseases; Affected: YES; Cells ...more +inquiry

ABC-SC2054

HighQC™ Human IPSC From Fibroblast-Long QT Syndrome 3

Long QT Syndrome 3; LQT3 SODIUM CHANNEL, VOLTAGE-GATED, TYPE V, ALPHA SUBUNIT; SCN5A; Subcollection:...more +inquiry

ABC-SC2053

HighQC™ Human IPSC From Fibroblast-Long QT Syndrome 2

Long QT Syndrome 2; LQT2 POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY H, MEMBER 2; KCNH2; Subcollecti...more +inquiry

ABC-SC2052

HighQC™ Human IPSC From Fibroblast-Krabbe Disease-Galactosylceramidase

Krabbe Disease, Galactosylceramidase; GALC; Subcollection: Heritable Diseases Lysosomal Storage Dise...more +inquiry
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