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Merck
CN

BX-0900-32

Human Microglia

Human iPSC line, Fully differentiated, Healthy Female Control (no known neurological disorders), Cryopreserved

Synonym(s):

Brain macrophages

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About This Item

Biological source:
human (iPSC line)
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biological source

human (iPSC line)

form

frozen liquid

packaging

vial of 1 (contains ≥1 million cells)

technique(s)

cell culture | mammalian: suitable

shipped in

liquid nitrogen

storage temp.

-140 to -196°C

General description

Human iPSC-Derived Microglia. Cells derived from male (BX-0900-30-1M) and female (BX-0900-32-1M) lines available. GFP-expressing neurons also available (BX-0901-30-1M). A major immune cell within the central nervous system (CNS), microglia are responsible for eliminating dead neurons, microbes, protein aggregates, and other particulates like degenerating synapses and myelin debris that are in the CNS. They also help to maintain neuronal networks, aid in injury repair, and mediate neuroinflammation. Microglia are implicated in neurodegeneration and aging, and are used to study autism, epilepsy, Alzheimer’s disease, and Huntington’s disease.

Application

Function: Human Microglia demonstrate phagocytosis and can be stimulated to secrete a variety of cytokines.

Features and Benefits

Marker Expression: Fully differentiated with confirmed expression of microglia surface markers including: CD45, CD11b, CX3CR1, P2RY12, and TMEM119. Immunocytochemistry shortly after plating microglia (shown here with a DAPI stain) reveals prominent expression of TREM2 (green) and IBA1 (red).


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Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Rezwanul Islam et al.
Translational stroke research, 16(3), 655-671 (2024-04-01)
Subarachnoid hemorrhage (SAH) accounts for 5% of stroke, with women having a decreased inflammatory response compared to men; however, this mechanism has yet to be identified. One hurdle in SAH research is the lack of human brain models. Studies in