Anti HSD17B4 pAb (ATL-HPA021479 w/enhanced validation)

Atlas Antibodies

Catalog No.:
ATL-HPA021479-100
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Protein Description: hydroxysteroid (17-beta) dehydrogenase 4
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