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Rabbit Anti-IQCC antibody
Rabbit Anti-IQCC antibody
IQ domain containing protein C; IQ domain-containing protein C; IQ motif containing C; Iqcc; IQCC_HUMAN.
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  • NO.:SL9019R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Mouse,(predicted: Human,Rat,Pig,Horse,)
    Applications:WB IHC-P IHC-F IF
    concentration:1mg/ml
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Details

Product Name IQCC
Chinese Name IQCC蛋白抗体
Alias IQ domain containing protein C; IQ domain-containing protein C; IQ motif containing C; Iqcc; IQCC_HUMAN.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Mouse,  (predicted: Human, Rat, Pig, Horse, )
Applications WB=1:500-2000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 53kDa
Cellular localization The nucleus cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human IQCC: 1-100/466 
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 Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

Similarity:
Contains 1 IQ domain.

SWISS:
Q4KMZ1

Gene ID:
55721

Database links:

Entrez Gene: 55721 Human

Entrez Gene: 230767 Mouse

SwissProt: Q4KMZ1 Human

SwissProt: A2ADZ8 Mouse

Unigene: 274356 Human

Unigene: 441132 Mouse



Product Picture
Sample:
Kidney (Mouse) Lysate at 40 ug
Primary: Anti- IQCC (SL9019R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 53 kD
Observed band size: 55 kD

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