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Location: Home > Antigen, Antibodies, ELISA, Western Blot > Primary Antibody > Polyclonal Antibodies > [KO Validated] AIF Polyclonal Antibody

[KO Validated] AIF Polyclonal Antibody

Catalog # Availability Size / Price Inquiry
APR24851N-1 50ul / $395
APR24851N-2 100ul / $495
APR24851N-3 200ul / $595

[KO Validated] AIF Polyclonal Antibody

Brand

Leading Biology

Catalog Number

APR24851N

Product Type

Polyclonal Antibodies

Field of Research

Cell Biology & Developmental Biology>Apoptosis

Product Overview

We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality [KO Validated] AIF Polyclonal Antibody.

Molecular Weight

Calculated MW: 26kDa/28kDa/35kDa/66kDa Observed MW: 67kDa

Species Reactivity

Rabbit

Immunogen

Recombinant fusion protein of human AIF (NP_004199.1).

Cross Reactivity

Human,Mouse,Rat

Isotype

IgG

GeneID

UniProt ID

Purity

Affinity purification

Storage & Stability

Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

Storage Buffer

Buffer: PBS with 50% glycerol, pH7.3.

Applications

WB,IHC,IF,IP

Dilution

WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200

Product Description

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.

Synonyms

AIFM1; AIF; CMT2D; CMTX4; COWCK; COXPD6; DFNX5; NADMR; NAMSD; PDCD8; apoptosis-inducing factor 1, mitochondrial

Images

Western blot analysis of extracts of various cell lines, using AIF antibody.

Western blot analysis of extracts from normal (control) and AIF knockout (KO) 293T cells, using AIF antibody.

Immunohistochemistry of paraffin-embedded rat lung using AIF antibody.

Specification

Quantity

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