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HPA066953

Sigma-Aldrich

Anti-YME1L1 antibody produced in rabbit

Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution

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About This Item

UNSPSC Code:
12352203
Human Protein Atlas Number:
NACRES:
NA.41

biological source

rabbit

Quality Level

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

product line

Prestige Antibodies® Powered by Atlas Antibodies

form

buffered aqueous glycerol solution

species reactivity

human

technique(s)

immunofluorescence: 0.25-2 μg/mL
immunohistochemistry: 1:500-1:1000

isotype

IgG

immunogen sequence

AVDGKEMVTMKELEFSKDKILMGPERRSVEIDNKNKTITAYHESGHAIIAYYTKDAMPINKATIMPRGPTLGHVSLLPENDRWNETRAQLLAQMDVS

UniProt accession no.

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... YME1L1(10730)

General description

ATP-dependent zinc metalloprotease YME1L1 is an enzyme encoded by YME1L1 gene. It belongs to the family of ATPases associated with a variety of cell activities (AAA family). In the human chromosome, it is localized on 10p12.1. YME1L is homologous to yeast YME1. The protein encoded by this gene has 716 amino acids.

Immunogen

YME1-like 1 ATPase

Application

All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project and as a result, are supported by the most extensive characterization in the industry.

The Human Protein Atlas project can be subdivided into three efforts: Human Tissue Atlas, Cancer Atlas, and Human Cell Atlas. The antibodies that have been generated in support of the Tissue and Cancer Atlas projects have been tested by immunohistochemistry against hundreds of normal and disease tissues and through the recent efforts of the Human Cell Atlas project, many have been characterized by immunofluorescence to map the human proteome not only at the tissue level but now at the subcellular level. These images and the collection of this vast data set can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. We also provide Prestige Antibodies® protocols and other useful information.
Anti-YME1L1 recognises YME1L1 protein.

Biochem/physiol Actions

ATP-dependent zinc metalloprotease YME1L1 protects the mitochondria, regulates the movement of proteins across the mitochondrial membrane and the proteolysis of misfolded proteins. It also controls the mitochondrial dynamics. YME1L1 controls the formation of respiratory chain molecules by proteolysis and maintains the cristae structure. YME1L1 helps mitochondria to adjust to different types of stress. In humans, mutations in YME1L1 leads to mitochondriopathy with optic nerve atrophy and mitochondrial network fragmentation. YME1L1 is associated with hereditary spastic paraplegia and other neurodegenerative disorders.

Features and Benefits

Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.

Every Prestige Antibody is tested in the following ways:
  • IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.
  • Protein array of 364 human recombinant protein fragments.

Linkage

Corresponding Antigen APREST88359

Physical form

Solution in phosphate-buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide.

Legal Information

Prestige Antibodies is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation
Hartmann B, et al.
eLife, 5(6), e16078-e16078 (2016)
New roles for mitochondrial proteases in health, ageing and disease
Quiros PM, et al.
Nature Reviews in Molecular and Cell Biology, 16(6), 345-345 (2015)
Pacifiplex: an ancestry-informative SNP panel centred on Australia and the Pacific region
Santos C, et al.
Forensic Science International. Genetics, 20, 71-80 (2016)
YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation
Stiburek L, et al.
Molecular Biology of the Cell, 23(6), 1010-1023 (2012)
Unmasking a temperature-dependent effect of the P. anserina i-AAA protease on aging and development
Weil A, et al.
Cell Cycle, 10(24), 4280-4290 (2011)

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