Product Name	Anti-MAP7D1/AF594
Chinese Name	AF594标记的精氨酸/脯氨酸富含卷曲蛋白1抗体
Alias	Arginine/proline rich coiled coil 1; Arginine/proline rich coiled coil domain containing protein 1; Arginine/proline-rich coiled-coil domain-containing protein 1; MA7D1_HUMAN; MAP7 domain containing 1; MAP7 domain containing protein 1; MAP7 domain-containing protein 1; MAP7D1; MGC117315; PARCC1; Proline arginine rich coiled coil 1; Proline/arginine rich coiled coil domain containing protein 1; Proline/arginine-rich coiled-coil domain-containing protein 1; RPRC1.
Research Area	Cell biology  immunology
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species
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	93kDa
Form	Lyophilized or Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human MAP7D1/RPRC1
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 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. Subcellular Location: Cytoplasm, cytoskeleton, spindle. Similarity: Belongs to the MAP7 family. Database links: Entrez Gene: 55700 Human SwissProt: Q3KQU3 Human Unigene: 356096 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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