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AIFM1 Antibody

CAT: 0864-A52403-50ULSize: 50 μLDry Ice: NoHazardous: No
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CAT#:0864-A52403-50ULSize:50 μL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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CAS Number
9007-83-4
Gene Aliases
AIFM1, AIFM1_HUMAN, Apoptosis inducing factor 1, mitochondrial, Apoptosis inducing factor, Apoptosis inducing factor, mitochondrion associated, 1, Apoptosis-inducing factor 1, CMTX4, COWCK, COXPD6, Harlequin, Hq, mAIF, MGC111425, MGC5706, mitochondrial, Neuropathy, axonal motor-sensory, with deafness and mental retardation, neuropathy, axonal, motor-sensory with deafness and mental retardation (Cowchock syndrome) , PDCD 8, PDCD8, Programmed cell death 8 (apoptosis inducing factor) , Programmed cell death 8, Programmed cell death 8 isoform 1, Programmed cell death 8 isoform 2, Programmed cell death 8 isoform 3, Programmed cell death protein 8, Programmed cell death protein 8 mitochondrial, Programmed cell death protein 8 mitochondrial precursor, Programmed cell death protein 8 mitochondrial precursor, Striatal apoptosis inducing factor
UniProt
O95831
Host
Rabbit
Antigen Species
Human
Reactivity
Human, Mouse, Rat
Target Antigen
Fusion protein of Human AIFM1
Target
AIFM1
Clonality
Polyclonal
Conjugation
Non-conjugated
Applications
ELISA, WB, IHC, ELISA:1:1000-1:2000, WB:1:200-1:1000, IHC:1:15-1:50
Field of Research
Cell Biology
Purification Method
Antigen affinity purified
Form
Liquid
Buffer
PBS, 0.05% sodium azide, 40% glycerol, pH 7.4.
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Fragment
IgG

UniProtKB · O95831

Apoptosis-inducing factor 1, mitochondrial

AIFM1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O95831
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
AIFM1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
1.6.99.-
Processing
Precursor
Secondary accessions
A4QPB4, B1ALN1, B2RB08, D3DTE9, E9PRR0, Q1L6K4, Q1L6K6, Q2QKE4, Q5JUZ7, Q6I9X6, Q9Y3I3, Q9Y3I4
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

AcetylationIsopeptide bondPhosphoproteinUbl conjugation

Coding sequence diversity

Alternative splicing

Biological process

Apoptosis

Disease

Charcot-Marie-Tooth diseaseDeafnessDisease variantDwarfismIntellectual disabilityNeurodegenerationNeuropathyPrimary mitochondrial disease

Cellular component

CytoplasmMembraneMitochondrionMitochondrion inner membraneNucleus

Molecular function

DNA-bindingOxidoreductase

Ligand

FADFlavoproteinNAD

Domain

Transit peptide

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