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Rabbit Anti-FKSG24/AF350 Conjugated antibody
Rabbit Anti-FKSG24/AF350 Conjugated antibody
FKSG 24; MGC110861; MGC12972; M17L2_HUMAN; MPV17 mitochondrial membrane protein like 2; MPV17L2; Uncharacterized protein FKSG24.
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Regular members: $476.8
  • NO.:SL16098R-AF350
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted:Human,Mouse,Rat,Dog,Pig,Cow,Horse,Sheep)
    Applications:ICC/IF,IF
    concentration:1mg/ml
  • Goods click count:389
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Product Name Anti-FKSG24/AF350
Chinese Name AF350标记的MPV17L2蛋白抗体
Alias FKSG 24; MGC110861; MGC12972; M17L2_HUMAN; MPV17 mitochondrial membrane protein like 2; MPV17L2; Uncharacterized protein FKSG24.
Research Area Cell biology immunology
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted:Human,Mouse,Rat,Dog,Pig,Cow,Horse,Sheep)
Applications ICC/IF=1:50-200,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 23kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FKSG24
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 1M TBS(pH7.4) with 1% BSA, 3% Proclin300 and 50% Glycerol
Storage 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 1M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 癈.
Product Detail background:
Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The MPV17L2 gene product has been provisionally designated MPV17L2 pending further characterization.

Function:
FKSG24 is a potential multi-pass membrane protein. It belongs to the peroxisomal membrane protein PXMP2/4 family. The exact function of FKSG24 remains unknown.

Subcellular Location:
Membrane; Multi-pass membrane protein (potential)

Similarity:
Belongs to the peroxisomal membrane protein PXMP2/4 family.

Database links:

Entrez Gene: 84769 Human

Entrez Gene: 234384 Mouse

SwissProt: Q567V2 Human

SwissProt: Q8VIK2 Mouse



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

Partial purchase records(bought amounts latest3)

UsernameQuantitybought time
Um***12024-08-08
Fr***22024-02-14
Ol***22023-10-09
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