Rabbit Anti-NDUFAF7/FITC Conjugated antibody

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C2orf56; Chromosome 2 open reading frame 56; MidA; MIDA_HUMAN; mitochondrial; Mitochondrial dysfunction protein A homolog; NADH dehydrogenase [ubiquinone] complex I, assembly factor 7; OTTHUMP00000158583; OTTHUMP00000201359; OTTHUMP00000201362;

Cat:

SL19078R-FITC

Species Reactivity：

(predicted: Human,Mouse,Rat,Dog,Pig,Cow,Horse,Rabbit,)

Immunogen：

KLH conjugated synthetic peptide derived from human NDUFAF7

Format：

Lyophilized or Liquid

Storage instructions：

Store at -20 癈 for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20癈. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antib

Buffer：

0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

Concentration：

1mg/ml

Clonality：

Polyclonal

Isotype：

IgG

Applications：

ICC=1:50-200IF=1:50-200not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.

Host：

Rabbit

Calculated MW：

44kDa

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Unit:

Price: $596.00

Product PDFs

Datasheet: Down Datasheet

Other Information
Citations
Protein Attributes
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background:
C12orf56 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鰉 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.

Function:
Involved in the assembly or stability of mitochondrial NADH:ubiquinone oxidoreductase complex (complex I).

Subunit:
Homodimer. Interacts with NDUFS2.

Subcellular Location:
Mitochondrion

Similarity:
Belongs to the NDUFAF7 family.

Database links:

Entrez Gene: 55471 Human

GenBank: NM_144736 Human

GenBank: NP_653337 Human

SwissProt: Q7L592 Human

Unigene: 433466 Human

Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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