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Rabbit Anti-GIDRP88/RBITC Conjugated antibody
Rabbit Anti-GIDRP88/RBITC Conjugated antibody
GIDRP86; C10orf28; Chromosome 10 open reading frame 28; FLJ25458; FLJ37160; Growth inhibition and differentiation related protein 86; PSORT; Putative mitochondrial space protein 32.1; R3HCL_HUMAN.
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Product Name Anti-GIDRP88/RBITC
Chinese Name 罗丹明(RBITC)标记的生长抑制和分化相关蛋白抗体
Alias GIDRP86; C10orf28; Chromosome 10 open reading frame 28; FLJ25458; FLJ37160; Growth inhibition and differentiation related protein 86; PSORT; Putative mitochondrial space protein 32.1; R3HCL_HUMAN.  
Research Area Cell biology  Developmental biology  Growth factors and hormones  Cyclin  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
Applications IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 88kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human GIDRP88
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Store at -20 °C 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°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Product Detail background:
C10orf28 is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

Tissue Specificity:
Expressed in placenta.

Database links:
UniProtKB/Swiss-Prot: Q7Z5L2.2

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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