NADH Dehydrogenase (Ubiquinone) Complex I, Assembly Factor 7 (NDUFAF7) anticorps (HRP)

Détails pour le produit réf. ABIN1712490, Fournisseur: Connectez-vous pour afficher
Antigène
  • C11H2orf56
  • 2410091C18Rik
  • AL033374
  • PRO1853
  • C2orf56
  • MidA
  • c2orf56
  • chromosome 11 open reading frame, human C2orf56
  • NADH dehydrogenase (ubiquinone) 1 alpha subcomplex assembly factor 7
  • NADH dehydrogenase (ubiquinone) complex I, assembly factor 7
  • NDUFAF7
  • Ndufaf7
  • ndufaf7
Reactivité
Humain, Souris, Rat (Rattus)
25
15
15
1
1
1
1
Hôte
Lapin
19
6
Clonalité
Polyclonal
Conjugué
HRP
1
1
1
1
1
1
1
1
1
1
1
1
1
Application
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
13
12
4
3
2
Options
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Supplier Product No.
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Immunogène KLH conjugated synthetic peptide derived from human C2orf56
Isotype IgG
Purification Purified by Protein A.
Autre désignation C2orf56
Sujet

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, Alstré° 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.

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.

ID gène 55471
Indications d'application WB 1:100-1000
IHC-P 1:100-500
Restrictions For Research Use only
Format Liquid
Concentration 1 μg/μL
Buffer Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % Gentamicin.
Agent conservateur Gentamicin sulfate
Précaution d'utilisation This product contains Gentamicin sulfate: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Conseil sur la manipulation Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
Stock 4 °C
Stockage commentaire Store at 4°C
Date de péremption 12 months
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