Anti HSD17B4 pAb (ATL-HPA021479 w/enhanced validation)
Atlas Antibodies
- Catalog No.:
- ATL-HPA021479-100
- Shipping:
- Calculated at Checkout
$593.00
Gene Name: HSD17B4
Alternative Gene Name: DBP, MFE-2, SDR8C1
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000024507: 92%, ENSRNOG00000015840: 93%
Entrez Gene ID: 3295
Uniprot ID: P51659
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
| Product Specifications | |
| Application | WB, IHC |
| Reactivity | Human |
| Clonality | Polyclonal |
| Host | Rabbit |
| Immunogen | VNNAGILRDRSFARISDEDWDIIHRVHLRGSFQVTRAAWEHMKKQKYGRIIMTSSASGIYGNFGQANYSAAKLGLLGLANSLAIEGRKSNIHCNTIAPNAGSRMTQTVMPEDLVEALKPEYVAPLV |
| Gene Sequence | VNNAGILRDRSFARISDEDWDIIHRVHLRGSFQVTRAAWEHMKKQKYGRIIMTSSASGIYGNFGQANYSAAKLGLLGLANSLAIEGRKSNIHCNTIAPNAGSRMTQTVMPEDLVEALKPEYVAPLV |
| Gene ID - Mouse | ENSMUSG00000024507 |
| Gene ID - Rat | ENSRNOG00000015840 |
| Buffer | 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative. |
| Documents & Links for Anti HSD17B4 pAb (ATL-HPA021479 w/enhanced validation) | |
| Datasheet | Anti HSD17B4 pAb (ATL-HPA021479 w/enhanced validation) Datasheet (External Link) |
| Vendor Page | Anti HSD17B4 pAb (ATL-HPA021479 w/enhanced validation) at Atlas Antibodies |
| Documents & Links for Anti HSD17B4 pAb (ATL-HPA021479 w/enhanced validation) | |
| Datasheet | Anti HSD17B4 pAb (ATL-HPA021479 w/enhanced validation) Datasheet (External Link) |
| Vendor Page | Anti HSD17B4 pAb (ATL-HPA021479 w/enhanced validation) |
| Citations for Anti HSD17B4 pAb (ATL-HPA021479 w/enhanced validation) – 2 Found |
| Chen, Kui; Yang, Ke; Luo, Su-Shan; Chen, Chen; Wang, Ying; Wang, Yi-Xuan; Li, Da-Ke; Yang, Yu-Jie; Tang, Yi-Lin; Liu, Feng-Tao; Wang, Jian; Wu, Jian-Jun; Sun, Yi-Min. A homozygous missense variant in HSD17B4 identified in a consanguineous Chinese Han family with type II Perrault syndrome. Bmc Medical Genetics. 2017;18(1):91. PubMed |
| Amor, David J; Marsh, Ashley P L; Storey, Elsdon; Tankard, Rick; Gillies, Greta; Delatycki, Martin B; Pope, Kate; Bromhead, Catherine; Leventer, Richard J; Bahlo, Melanie; Lockhart, Paul J. Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency. Neurology. Genetics. 2016;2(6):e114. PubMed |