Web基因名. Exph5. 基因曾用名. Slac2b， slac2-b， Kiaa0624， E030050P12， B130009M24Rik， AC079869.22gm5. WebAntibodies that detect EXPH5 can be used in several scientific applications, including Western Blot and Immunohistochemistry. These antibodies target EXPH5 in Human samples. Our EXPH5 polyclonal antibodies are developed in Rabbit. Find the EXPH5 antibody that fits your needs. Choose from 1 of 3 EXPH5 antibodies, which have been …

ACKR1 Gene - GeneCards ACKR1 Protein ACKR1 Antibody

Webkrt5基因突变为本病的致病原因 ，也可由krt14和exph5基因突变引起 [4,5] 。本病例测序结果显示，先证者及其父亲携带krt5基因c.74c>t突变，与该病的高频突变位点一致 。 Web1、由原核基因编码的基因产物必须与同转染前真核细胞内任何相似的产物相区别；. 2、细胞内其它的基因产物不会干扰报告基因产物的检测；. 3、报告基因编码的产物的检测应该快速、简便、灵敏度高而且重现性好。. 报告基因的种类很多，根据对其表达产物的 ... nike sweatpants outfits tumblr

Mutations in EXPH5 result in autosomal recessive inherited skin ...

WebEXPH5: Exophilin 5: Protein Coding: 43: GC11M108505: 37.62: 2: POGLUT3: Protein O-Glucosyltransferase 3: Protein Coding: 40: GC11M108473: 7.42: 3: DDX10: DEAD-Box … WebExophilin 5, also known as EXPH5, is a human gene. Interactions. EXPH5 has been shown to interact with RAB27A. References ^ a b c GRCh38: Ensembl release 89: ENSG00000110723 - Ensembl, May 2024 ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000034584 - Ensembl, May 2024 ^ "Human PubMed Reference:". WebJan 22, 2013 · McGrath et al. (2012) studied an Iraqi family in which 3 of 8 sibs born to first-cousin parents had inherited skin fragility and mutation in the EXPH5 gene. The clinical features were apparent from early childhood and consisted primarily of trauma-induced scale crusts and intermittent skin blistering that was mostly secondary to trauma, such as … nth-of-type和nth-child区别