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- 规格参数
- 包装参数
General description
This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. (provided by RefSeq)
Immunogen
WBSCR18 (AAH05056, 1 a.a. ~ 226 a.a) full-length human protein.
Sequence
MAAMRWRWWQRLLPWRLLQARGFPQNSAPSLGLRARTYSQGDCSYSRTALYDLLGVPSTATQAQIKAAYYRQCFLYHPDRNSGSAEAAERFTRISQAYVVLGSATLRRKYDRGLLSDEDLRGPGVRPSRTPAPDPGSPRTPPPTSRTHDGSRASPGANRTMFNFDAFYQAHYGEQLERERRLRARREALRKRQEYRSMKGLRWEDTRDTAAIFLIFSIFIIIGFYI
Physical form
Solution in phosphate buffered saline, pH 7.4
| biological source | mouse |
| Quality Segment | 100 |
| conjugate | unconjugated |
| antibody form | purified immunoglobulin |
| antibody product type | primary antibodies |
| clone | polyclonal |
| form | buffered aqueous solution |
| mol wt | antigen 26.1 kDa |
| species reactivity | human |
| technique(s) | immunofluorescence: suitable,western blot: 1 μg/mL |
| NCBI accession no. | BC005056 |
| shipped in | dry ice |
| storage temp. | −20°C |
| target post-translational modification | unmodified |
| Gene Information | human ... WBSCR18(84277) |
| 长度(mm) | |
| 宽度(mm) | |
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| 重量(kg) |
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¥ 1451.54
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¥ 4039.86
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¥ 2573.97
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¥ 2268.97
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¥ 2307.00
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¥ 787.34
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¥ 5804.96
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¥ 2288.54
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¥ 4476.05
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¥ 14985.93
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¥ 3704.60
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