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Rabbit Anti-EMID1/PE-Cy3 Conjugated antibody
Rabbit Anti-EMID1/PE-Cy3 Conjugated antibody
AW122071; CO 5; CTA-984G1.2; EMI domain containing 1; EMI domain containing protein 1; EMI domain-containing protein 1; EMI5; EMID 1; Emid1; EMID1_HUMAN; Emilin and multimerin domain containing protein 1; Emilin and multimerin domain-containing protein 1;
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  • NO.:SL14581R-PE-Cy3
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Rat,(predicted: Human,Mouse,Dog,Cow,)
    Applications:ICC IF
    concentration:1mg/ml
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Product Name Anti-EMID1/PE-Cy3
Chinese Name PE-Cy3标记的EMID1蛋白抗体
Alias AW122071; CO 5; CTA-984G1.2; EMI domain containing 1; EMI domain containing protein 1; EMI domain-containing protein 1; EMI5; EMID 1; Emid1; EMID1_HUMAN; Emilin and multimerin domain containing protein 1; Emilin and multimerin domain-containing protein 1; EMU1; hEmu1; MGC50657; OTTMUSP00000005297; Protein Emu1; Putative emu1; RGD1565846; RP23-338J18.3.  
Research Area Tumour  Cell biology  Neurobiology  Signal transduction  Cell type markers  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Rat,  (predicted: Human, Mouse, Dog, Cow, )
Applications ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 43kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human EMID1
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:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

Subunit:
Homo- or heteromers.

Subcellular Location:
Secreted; extracellular space; extracellular matrix.

Similarity:
Contains 1 collagen-like domain.
Contains 1 EMI domain.

Database links:

Entrez Gene: 129080 Human

Entrez Gene: 140703 Mouse

Entrez Gene: 685462 Rat

Omim: 608926 Human

SwissProt: Q96A84 Human

SwissProt: Q91VF5 Mouse

Unigene: 289106 Human

Unigene: 840 Mouse

Unigene: 81507 Rat



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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