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ITM0017

ITM0017
ITM0017
from
$556.00
Price in reward points: 556
  • Catalog: ITM0017
  • Gene/Protein: AIFM1
  • Product Description: Immunotag™ AIF-M1 Monoclonal Antibody

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Immunotag™ AIF-M1 Monoclonal Antibody
Antibody Specification
Datasheet
IMPORTANT NOTE This product is custom manufactured with a lead time of 3-4 weeks. Once in production, this item cannot be cancelled from an order and is not eligible for return.
Target Protein AIF-M1
Clonality Monoclonal
Storage/Stability -20°C/1 year
Application WB,IHC-p,IF,FCM,ELISA
Recommended Dilution Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/200 - 1/1000. Immunofluorescence: 1/200 - 1/1000. Flow cytometry: 1/200 - 1/400. ELISA: 1/10000. Not yet tested in other applications.
Concentration 1 mg/ml
Reactive Species Human,Mouse,Rat,Monkey
Host Species Mouse
Immunogen Purified recombinant fragment of human AIF-M1 expressed in E Coli
Specificity AIF-M1 Monoclonal Antibody detects endogenous levels of AIF-M1 protein.
Purification Affinity purification
Form Ascitic fluid containing 0.03% sodium azide.
Gene Name AIFM1
Accession No. O95831 Q9Z0X1 Q9JM53
Alternate Names AIFM1; AIF; PDCD8; Apoptosis-inducing factor 1; mitochondrial; Programmed cell death protein 8
Description apoptosis inducing factor, mitochondria associated 1(AIFM1) Homo sapiens This gene encodes a flavoprotein essential for nuclear disassembly in apoptotic cells, and it is found in the mitochondrial intermembrane space in healthy cells. Induction of apoptosis results in the translocation of this protein to the nucleus where it affects chromosome condensation and fragmentation. In addition, this gene product induces mitochondria to release the apoptogenic proteins cytochrome c and caspase-9. Mutations in this gene cause combined oxidative phosphorylation deficiency 6 (COXPD6), a severe mitochondrial encephalomyopathy, as well as Cowchock syndrome, also known as X-linked recessive Charcot-Marie-Tooth disease-4 (CMTX-4), a disorder resulting in neuropathy, and axonal and motor-sensory defects with deafness and mental retardation. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome
Cell Pathway/ Category Apoptosis_Inhibition,Apoptosis_Mitochondrial,Apoptosis_Overview,
Protein Expression Brain,Colon,Kidney,Ovary,
Subcellular Localization cell,nucleus,mitochondrion,mitochondrial inner membrane,mitochondrial intermembrane space,cytosol,integral component of membrane,perinuclear region of cytoplasm,
Protein Function catalytic activity:2 glutathione + protein-disulfide = glutathione disulfide + protein-dithiol.,cofactor:FAD.,function:Possesses significant protein thiol-disulfide oxidase activity.,function:Probable oxidoreductase that acts as a caspase-independent mitochondrial effector of apoptotic cell death. Extramitochondrial AIF induces nuclear chromatin condensation and large scale DNA fragmentation (in vitro). Binds to DNA in a sequence-independent manner.,similarity:Belongs to the FAD-dependent oxidoreductase family.,similarity:Contains 1 thioredoxin domain.,subcellular location:Translocated to the nucleus upon induction of apoptosis.,subunit:Interacts with XIAP.,tissue specificity:Widely expressed.,
Usage For Research Use Only! Not for diagnostic or therapeutic procedures.

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