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Abnova
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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Product may be used with Western Blot (Transfected lysate).
The Isotype of this product is composed of an IgG Mixture.
Immunogen sequence: MAAMRWRWWQ RLLPWRLLQA RGFPQNSAPS LGLRARTYSQ GDCSYSRTAL YDLLGVPSTA TQAQIKAAYY RQCFLYHPDR NSGSAEAAER FTRISQAYVV LGSATLRRKY DRGLLSDEDL RGPGVRPSRT PAPDPGSPRT PPPTSRTHDG SRASPGANRT MFNFDAFYQA HYGEQLERER RLRARREALR KRQEYRSMKG LRWEDTRDTA AIFLIFSIFI IIGFYI
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: DnaJ (Hsp40) homolog, subfamily C, member 30; DnaJ homolog subfamily C member 30, mitochondrial; similar to DNAJ; unnamed protein product; Williams Beuren syndrome chromosome region 18; Williams-Beuren syndrome chromosomal region 18 protein
基因别名: DNAJC30; LHONAR; LHONAR1; MC1DN38; WBSCR18
UniProt ID: (Human) Q96LL9
Entrez Gene ID: (Human) 84277