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AG10774 Endothelial from Vein, iliac

Description:

APPARENTLY HEALTHY INDIVIDUAL

Affected:

No

Sex:

Male

Age:

22 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIA Aging Cell Culture Repository
Subcollection Apparently Healthy Collection
Biopsy Source Vein, iliac
Cell Type Endothelial
Tissue Type Vein
Transformant Untransformed
Sample Source Endothelial from Vein, iliac
Race White
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Line HIVE-87. The iliac vein was removed from a braindead, heartbeating cadaver, organ donor on 6/09/87. The donor died of a closed head trauma and had no known diseases. The culture was initiated on 6/09/87 using cells released from the lumen of the vessel by collagenase digestion. Cell morphology is polygonal. This culture tested positive for the endothelial cell-specific von Willebrand factor and negative for alphasmooth muscle actin (immunofluorescence assays). The culture was grown on gelatin-coated flasks and the medium was supplemented with 0.02 mg/ml ECGS and 0.05 mg/ml heparin. Cells were frozen in growth medium containing 7.5% polyvinylpyrrolidinone and 5% DMSO.

Characterizations

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PDL at Senescence 27
PDL at Freeze 18
Passage Frozen 6
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 

Phenotypic Data

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Remarks Line HIVE-87. The iliac vein was removed from a braindead, heartbeating cadaver, organ donor on 6/09/87. The donor died of a closed head trauma and had no known diseases. The culture was initiated on 6/09/87 using cells released from the lumen of the vessel by collagenase digestion. Cell morphology is polygonal. This culture tested positive for the endothelial cell-specific von Willebrand factor and negative for alphasmooth muscle actin (immunofluorescence assays). The culture was grown on gelatin-coated flasks and the medium was supplemented with 0.02 mg/ml ECGS and 0.05 mg/ml heparin. Cells were frozen in growth medium containing 7.5% polyvinylpyrrolidinone and 5% DMSO.

Publications

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Admasu TD, Kim K, Rae M, Avelar R, Gonciarz RL, Rebbaa A, Pedro de Magalhães J, Renslo AR, Stolzing A, Sharma A, Selective ablation of primary and paracrine senescent cells by targeting iron dyshomeostasis Cell reports42:112058 2022
PubMed ID: 36753419

External Links

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dbSNP dbSNP ID: 21534

Culture Protocols

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PDL at Senescence 27
Cumulative PDL at Freeze 18
Passage Frozen 6
Split Ratio 1:5
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Medium 199 in Earl BSS with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Heat Inactivated
Substrate Gelatin
Subcultivation Method trypsin-EDTA
Supplement Endothelial Cell Growth Supplement 0.02 mg/ml
Supplement Heparin 0.05 mg/ml
Pricing
Commercial:
$257.00USD
Academic &
Non-profit:
$103.00USD
NIA Grantees:
$47.00USD
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