CTTNBP2NL Polyclonal Antibody, FITC Conjugated
Catalogue Number: BS-14108R-FITC-BSS
| Manufacturer: | Bioss Inc |
| Type: | Polyclonal Primary Antibody - Conjugated |
| Alias: | CT2NL_HUMAN; CTTNBP2 N terminal like; CTTNBP2 N terminal like protein; CTTNBP2 N-terminal-like protein; Cttnbp2nl; DKFZp547A023; FLJ13278; KIAA1433. |
| Shipping Condition: | Blue Ice |
| Unit(s): | 100 ul |
| Host name: | Rabbit |
| Clone: | |
| Isotype: | IgG |
| Immunogen: | KLH conjugated synthetic peptide derived from human CTTNBP2NL |
| Application: | ICC, IF, IHC-P, WB, IHC-Fr |
Description
Description: CTTNBP2NL is a 639 amino acid protein that is encoded by a gene that maps to human chromosome 1p13.2. 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.
Additional Text
Gene Name
CTTNBP2NL
Uniprot ID
Q9P2B4
Gene ID
55917
Purification
Protein A purified
Concentration
1 ug/ul
Antibody Clonality
Polyclonal
Modification
Unmodified
Storage Note
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Excitation
494nm/518nm
bs-14108R-FITC Datasheet
SUPPORT
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PRODUCT
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DELIVERY
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