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Rabbit Anti-TMA16 antibody
Rabbit Anti-TMA16 antibody
C4orf43; Chromosome 4 open reading frame 43; FLJ5295; Hypothetical protein FLJ11184; Hypothetical protein LOC55319; TMA16; TMA16_HUMAN; Translation machinery-associated protein 16; UPF0534 protein C4orf43.
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  • NO.:SL13180R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Chicken,Dog,Pig,Cow,Horse,Sheep,)
    Applications:WB ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Details

Product Name TMA16
Chinese Name 4号染色体开放阅读框43/FLJ11184抗体
Alias C4orf43; Chromosome 4 open reading frame 43; FLJ5295; Hypothetical protein FLJ11184; Hypothetical protein LOC55319; TMA16; TMA16_HUMAN; Translation machinery-associated protein 16; UPF0534 protein C4orf43.  
Research Area Tumour  Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Sheep, )
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 24kDa
Cellular localization The nucleus 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FLJ11184/C4orf43: 101-203/203 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The FLJ11184 gene product has been provisionally designated FLJ11184 pending further characterization.

Function:
The function of the hypothetical protein FLJ11184 is unknown.

Similarity:
Belongs to the UPF0534 family.

SWISS:
Q96EY4

Gene ID:
55319

Database links:

Entrez Gene: 55319 Human

SwissProt: Q96EY4 Human

Unigene: 267446 Human



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