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Rabbit Anti-C18orf1/APC Conjugated antibody
Rabbit Anti-C18orf1/APC Conjugated antibody
C18orf1; chromosome 18 open reading frame 1; clone 22; CR001_HUMAN; hypothetical protein LOC753; Uncharacterized protein C18orf1.
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  • NO.:SL9652R-APC
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Cow,Sheep,)
    Applications:ICC IF
    concentration:1mg/ml
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Details

Product Name Anti-C18orf1/APC
Chinese Name APC标记的18号染色体开放阅读框1抗体
Alias C18orf1; chromosome 18 open reading frame 1; clone 22; CR001_HUMAN; hypothetical protein LOC753; Uncharacterized protein C18orf1.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Cow, Sheep, )
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 34kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human C18orf1
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:
C18orf1 is a 306 amino acid single-pass membrane protein that contains one LDL-receptor class A domain and belongs to the PMEPA1 family. C18orf1 exists as five alternatively spliced isoforms that display selective expression and are encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.

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

Tissue Specificity:
Expressed in lymphocytes.

Similarity:
Belongs to the PMEPA1 family.
Contains 1 LDL-receptor class A domain.

Database links:

Entrez Gene: 753 Human

Omim: 606571 Human

SwissProt: O15165 Human

Unigene: 149363 Human



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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