Anti-NDUFAF7 antibody
| 英文名称 | NDUFAF7 |
| 中文名称 | NDUFAF7蛋白抗体 |
| 别 名 | C2orf56; Chromosome 2 open reading frame 56; MidA; MIDA_HUMAN; mitochondrial; Mitochondrial dysfunction protein A homolog; NADH dehydrogenase [ubiquinone] complex I, assembly factor 7; PRO1853; Protein midA homolog; Protein midA homolog, mitochondrial. |
DATASHEET
Host:Rabbit
Target Protein:NDUFAF7
IR:Immunogen Range:21-120/441
Clonality:Polyclonal
Isotype:IgG
Entrez Gene:55471
Swiss Prot:Q7L592
Source:KLH conjugated synthetic peptide derived from human NDUFAF7:21-120/441
Purification:affinity purified by Protein A
Storage:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
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.
Size:100ul
Concentration:1mg/ml
Applications:ELISA(1:5000-10000)
IHC-P(1:100-500)
IHC-F(1:100-500)
ICC(1:100-500)
IF(1:100-500)
Cross Reactive Species:Human
Mouse
Rat
Dog
Pig
Cow
Horse
Rabbit
.
For research use only. Not intended for diagnostic or therapeutic use.
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