NDUFAF7 antibody (AA 101-200) (HRP)

Catalog No. ABIN1712490

Product Details anti-NDUFAF7 Antibody (HRP)

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

Binding Specificity: AA 101-200

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NDUFAF7 antibody is conjugated to HRP

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro))

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: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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 (NDUFAF7 Products)

Synonyms: C11H2orf56 antibody, 2410091C18Rik antibody, AL033374 antibody, PRO1853 antibody, C2orf56 antibody, MidA antibody, c2orf56 antibody, NADH:ubiquinone oxidoreductase complex assembly factor 7 antibody, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex assembly factor 7 antibody, NADH:ubiquinone oxidoreductase complex assembly factor 7 S homeolog antibody, NDUFAF7 antibody, Ndufaf7 antibody, ndufaf7.S antibody

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