Apoptosis Inducing Factor 1, Mitochondrial (AIFM1) Peptide

Este producto es parte de AIFM - Apoptosis inducing factor mitochondria associated
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175.5€ (100 µg)

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935106861
info@markelab.com
name
Apoptosis Inducing Factor 1, Mitochondrial (AIFM1) Peptide
category
Proteins and Peptides
provider
Abbexa
reference
abx617277
tested applications
P-ELISA

Description

Apoptosis Inducing Factor 1, Mitochondrial (AIFM1) Peptide is a synthetic peptide. 

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Proteins and Peptides
Immunogen Target
Apoptosis Inducing Factor 1, Mitochondrial (AIFM1)
Host
Synthetic
Recommended Dilution
BL (predicted): 0.5 mg/ml. Optimal dilutions/concentrations should be determined by the end user.
Conjugation
Unconjugated
Observed MW
Sequence Fragment: Internal region, 183-195 AA: C-DDPNVTKTLRFKQ
Size 1
100 µg
Form
Lyophilized Reconstitute in deionized water.
Tested Applications
P-ELISA
Buffer
Prior to lyophilization: Deionized water.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Gene ID
9131
NCBI Accession
NP_004199.1, NP_665811.1, NP_001124319.1
Alias
AIFM1,AIF,CMT2D,CMTX4,COWCK
Background
Protein AIFM1
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

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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 10.

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