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微信小章| 产品名称： | p22/34 |
|---|---|
| 商品货号： | TS171566 |
| Designations： | p22/34 |
| Species： | Homo sapiens, human |
| Vector： | Construct size (kb): 4.5 |
| Insert： | DNA: genomic Insert lengths(kb): 1.799999952316284 Tissue: lymphoblast GM1416 (48,XXXX) cell line Gene product: DNA Segment, single copy D22S9 Alleles: B1, B2, A1, A2 |
| Insert Size (kb)： | 1.800 |
| Biosafety Level： | 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Shipping Information： | Distributed: DNA (dried). Rehydrate with TE. (amount: 2 ug) |
| Comments： | Restriction digests of the clone give the following sizes (kb): EcoRI--4.5; HindIII--4.5; BamHI--uncut; PstI--3.2, 1.4; SalI--uncut; EcoRI/HindIII--2.7, 1.8. D22S9 sequences are present in the marker bisatellited chromosome associated with cat eye syndrome. W21G (ATCC 61628, 61629) and p22/34 (ATCC 61576, 61577) hybridize to the same pair of SacII fragments and therefore cannot be separated by more than 380 kb. |
| References： | McDermid HE, et al. Characterization of the supernumerary chromosome in cat eye syndrome. Science 232: 646-648, 1986. PubMed: 3961499 Carey AH, et al. Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome. Genomics 7: 299-306, 1990. PubMed: 2365351 Duncan AM, et al. Breakpoint localization of the marker chromosome associated with the cat eye syndrome. Am. J. Hum. Genet. 38: 978-980, 1986. PubMed: 3088989 |