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Rabbit Anti-C4orf34  antibody
Rabbit Anti-C4orf34 antibody
Chromosome 4 open reading frame 34; Uncharacterized protein C4orf34; SIM14_HUMAN.
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  • NO.:SL15192R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Chicken,Dog,Cow,)
    Applications:IHC-P IHC-F ICC IF
    concentration:1mg/ml
  • Goods click count:62
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Details

Product Name C4orf34
Chinese Name 4号染色体开放阅读框34抗体
Alias Chromosome 4 open reading frame 34; Uncharacterized protein C4orf34; SIM14_HUMAN.   
Research Area Tumour  Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Chicken, Dog, Cow, )
Applications 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 11kDa
Cellular localization cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human C4orf34 : 1-50/99 
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 C4orf34 (chromosome 4 open reading frame 34) is a 99 amino acid single-pass membrane protein that is encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is located on chromosome 4. FGFR-3 is also encoded by a gene that maps to human 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.

Subcellular Location:
Membrane; Single-pass membrane protein (Potential).

SWISS:
Q96QK8

Gene ID:
201895

Database links:

Entrez Gene: 201895 Human

Entrez Gene: 68552 Mouse

Entrez Gene: 364154 Rat

SwissProt: Q96QK8 Human

SwissProt: Q91VT8 Mouse

SwissProt: Q498C7 Rat

Unigene: 576320 Human



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