Product Name	GRRP1
Chinese Name	GRRP1蛋白抗体
Alias	FAM110D; Family with sequence similarity 110, member D; Glycine/arginine-rich protein 1; GRPP1_HUMAN; GRRP1; Protein FAM110D; RP11-96L14.5.
Research Area	Cell biology  immunology
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	(predicted: Human, Mouse, Rat, Pig, Cow, Horse, Rabbit, Sheep, )
Applications	ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （Paraffin sections need antigen repair） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight	29kDa
Cellular localization	The nucleus
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human GRRP1: 51-150/271
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	GRRP1 (glycine/arginine-rich protein 1), also known as FAM110D, is a 271 amino acid protein encoded by a gene that maps to human chromosome 1p36.11 and mouse chromosome 4 D3. 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. Similarity: Belongs to the FAM110 family. SWISS: Q8TAY7 Gene ID: 79927 Database links: Entrez Gene: 79927 Human Entrez Gene: 72690 Mouse Entrez Gene: 500563 Rat SwissProt: Q8TAY7 Human SwissProt: Q80X91 Mouse Unigene: 694119 Human

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