NDUFAF7 antibody (AA 101-200) (AbBy Fluor® 750)

Catalog No. ABIN4998396

This Rabbit Polyclonal antibody specifically detects NDUFAF7 in WB, IF (cc) and IF (p). It exhibits reactivity toward Human.

Quick Overview for NDUFAF7 antibody (AA 101-200) (AbBy Fluor® 750) (ABIN4998396)

Target: NDUFAF7 (NADH Dehydrogenase (Ubiquinone) Complex I, Assembly Factor 7 (NDUFAF7))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NDUFAF7 antibody is conjugated to AbBy Fluor® 750

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-NDUFAF7 Antibody (AbBy Fluor® 750)

Binding Specificity: AA 101-200

Predicted Reactivity: Human,Mouse,Rat,Cow,Sheep,Pig,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C2orf56

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for NDUFAF7

Target: NDUFAF7 (NADH Dehydrogenase (Ubiquinone) Complex I, Assembly Factor 7 (NDUFAF7))

Alternative Name: C2orf56

Background:

Synonyms: C2orf56, Chromosome 2 open reading frame 56, MidA, MIDA_HUMAN, mitochondrial, Mitochondrial dysfunction protein A homolog, OTTHUMP00000158583, OTTHUMP00000201359, OTTHUMP00000201362, PRO1853, Protein midA homolog, Protein midA homolog, mitochondrial.

Background: C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

Gene ID: 55471