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AB258881

Human GHITM (MICS1) knockout HEK-293T cell lysate

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GHITM KO cell lysate available now. KO validated by. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, Homozygous: Insertion of the selection cassette in exon 2.

View Alternative Names

DERP2, Dermal papilla-derived protein 2, GHITM_HUMAN, Growth hormone-inducible transmembrane protein, HSPC282, MICS1, Mitochondrial morphology and cristae structure 1, My021, PTD010, TMBIM5, Transmembrane BAX inhibitor motif containing 5, Transmembrane BAX inhibitor motif-containing protein 5

1 Images
Sanger Sequencing - Human GHITM (MICS1) knockout HEK-293T cell lysate (AB258881)
  • Sanger seq

Unknown

Sanger Sequencing - Human GHITM (MICS1) knockout HEK-293T cell lysate (AB258881)

Homozygous : Insertion of the selection cassette in exon 2

Key facts

Cell type

HEK-293T

Species or organism

Human

Tissue

Kidney

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, Homozygous: Insertion of the selection cassette in exon 2.

Product details

Knockout cell lysate achieved by CRISPR/Cas9.

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.

User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.

This product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.

What's included?

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Properties and storage information

Gene name
GHITM
Gene editing type
Knockout
Gene editing method
CRISPR technology
Knockout validation
Sanger Sequencing
Zygosity
Homozygous
Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

MICS1 also known as mitochondrial import inner membrane translocase subunit 13 is a protein that plays a role in the transport of polypeptides across the mitochondrial inner membrane. It has an approximate mass of 13 kDa. You can find MICS1 expression predominantly in tissues with high-energy demands such as muscle and brain tissues where efficient mitochondrial function is critical.
Biological function summary

MICS1 contributes to the establishment of the mitochondrial inner membrane potential essential for maintaining proper mitochondrial function. MICS1 forms part of the translocase of inner membrane (TIM) complex which facilitates the import of preproteins into the mitochondria. This activity supports cellular energy metabolism by ensuring efficient electron transport chain operation and ATP production.

Pathways

MICS1 is involved in the mitochondrial protein import pathway and the maintenance of mitochondrial membrane potential. It interacts with other components of the TIM complex such as Tim23 and works closely with proteins in the oxidative phosphorylation pathway. These interactions ensure a seamless integration of imported mitochondrial proteins into the inner membrane facilitating cellular energy production processes.

MICS1 has links to conditions related to mitochondrial dysfunction such as mitochondrial myopathy and Leigh syndrome. Dysregulation of MICS1 may disrupt mitochondrial protein import and membrane potential maintenance contributing to these conditions. Its interaction with other mitochondrial proteins like Tim23 further associates it with the broader mitochondrial dysfunction often present in these diseases.

Quality control

STR analysis

CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX

Cell culture

Biosafety level

EU: 2 US: 2

Adherent/suspension

Adherent

Gender

Female

Product protocols

Product promise

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