Name : CCDC17 Antibody
Supplier : BIOSS PRIMARY UNCONJUGATED ANTIBODIES
Price :263
SKU : GEN6873415200
| Long name | CCDC17 Primary Polyclonal Antibody |
| Also known as | CCDC17 PAb |
| Category | Primary Antibodies |
| Conjugation | Unconjugated |
| Target Antigen | CCDC17 |
| Specificity | This is a highly specific antibody against CCDC17 |
| Modification(s) | None |
| Modification site(s) | Unmodified antibody |
| Clonality | Polyclonal antibody |
| Clone number | Polyclonal antibody |
| Concentration | 1ug per 1ul |
| Source | This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human CCDC17 |
| Gene ID number | 149483 |
| Tested Applications | IF(IHC-P), IHC-P, WB |
| Recommended dilutions | IF(IHC-P)(1:50-200), IHC-P(1:100-500), WB(1:100-1000) |
| Cross reactivity | Mouse, Rat, Human |
| Cross reactive species details | not every possible cross-reactivity is known, Due to limited amount of testing and knowledge |
| Background of the target antigen | 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, Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome, Gaucher disease and Usher syndrome are also associated with chromosome 1, Notably, Parkinsons, Stickler syndrome, The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis, The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration, There are about 3, When defective, also known as FLJ17921 or RP4-697E16, and considering the great number of genes there are also a large number of diseases associated with chromosome 1, is a 622 amino acid protein expressed as four isoforms and encoded by a gene mapping to human chromosome 1, malignant melanoma and multiple myeloma, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A, 000 genes on chromosome 1, 4, CCDC17 |
| Purification method | This antibody was purified via Protein A |
| Storage conditions | 50% glycerol and 0, Store at -20°, 09% sodium azide, C for up to 1 year, Keep the antibody in aqueous buffered solution containing 1% BSA |
| Synonym names | CCDC17, Coiled coil domain containing 17, Coiled-coil domain-containing protein 17, RP23-233B9, RP4-697E16, 4, 8, CCD17_HUMAN |
| Properties | C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Unconjugated Antibodies they should be stored frozen at - 24° |
| Gene target | CCDC17 |
| Short name | CCDC17 Antibody |
| Technique | antibodies against human proteins, antibodies for, Antibody |
| Alternative name | CCDC17 (Antibody to) |
| Alternative technique | antibodies |
| Identity | 26574 |
| Gene | CCDC17 |
| Long gene name | coiled-coil domain containing 17 |
| Synonyms | FLJ33084 |
| Locus | 1p34, 1 |
| Discovery year | 2005-05-13 |
| Entrez gene record | 149483 |
| RefSeq identity | NM_152500 |
| Havana BLAST/BLAT | OTTHUMG00000007822 |