Osteopetrosis Associated Transmembrane Protein 1 (OSTM1) ELISA试剂盒

OSTM1 encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. 再加上,我们可以发OSTM1 抗体 (52)OSTM1 蛋白 (10)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
OSTM1 28962 Q86WC4
OSTM1 14628 Q8BGT0
大鼠 OSTM1 OSTM1 499474  

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Human Osteopetrosis Associated Transmembrane Protein 1 (OSTM1) interaction partners

  1. KIF5B (显示 KIF5B ELISA试剂盒) is essential for Ostm1 intracellular dispersion.

  2. Ostm1 has a primary and autonomous role in neuronal homeostasis

  3. Common gating underlies the slow voltage activation of ClC-7 (显示 CLCN7 ELISA试剂盒).

  4. we describe for the first time homozygous microdeletions of different sizes affecting the OSTM1 gene in two unrelated consanguineous families with children suffering from neuronopathic infantile malignant osteopetrosi

  5. The authors show that both the aminoterminus and transmembrane span of the Ostm1 beta-subunit (显示 POLG ELISA试剂盒) are required for ClC-7 (显示 CLCN7 ELISA试剂盒) Cl(-)/H(+)-exchange, whereas the Ostm1 transmembrane domain suffices for its ClC-7 (显示 CLCN7 ELISA试剂盒)-dependent trafficking to lysosomes.

  6. mutation in the human GL gene leads to severe recessive osteopetros (显示 CSF1 ELISA试剂盒)is

  7. The human GIPN gene has 6 exons and 5 introns, and encodes a 334-aa protein.

  8. A novel mutation affecting the OSTM1 locus responsible for ARO (显示 CYP19A1 ELISA试剂盒). In addition to common clinical features of osteopetrosis (显示 CSF1 ELISA试剂盒), the patient developed a unique neuronal pathology that provided evidence for the role of OSTM1 in normal neuronal cell development.

  9. This study reports on a 12-month-old female with recessive OSMT1 mutations and neuroimaging findings suggesting a malignant infantile osteopetrosis (显示 CSF1 ELISA试剂盒).

  10. mutations in OSTM1 such as the C-terminal deletion mutant studied herein provoke dysregulation of the canonical Wnt (显示 WNT2 ELISA试剂盒)/beta-catenin (显示 CTNNB1 ELISA试剂盒) signaling pathway, providing a molecular basis for severe autosomal recessive osteopetrosis (显示 CSF1 ELISA试剂盒)

Mouse (Murine) Osteopetrosis Associated Transmembrane Protein 1 (OSTM1) interaction partners

  1. KIF5B (显示 KIF5B ELISA试剂盒) is essential for Ostm1 intracellular dispersion.

  2. Truncated OSTM1 significantly inhibited the expression of osteoclast marker genes through the down-regulation of the BLIMP1 (显示 PRDM1 ELISA试剂盒)-NFATc1 (显示 NFATC1 ELISA试剂盒) axis.

  3. Our in vivo structure-function analysis of ClC-7 (显示 CLCN7 ELISA试剂盒) reveals that both protein-protein interactions and ion transport must be considered in the pathogenesis of ClC-7 (显示 CLCN7 ELISA试剂盒)-related diseases.

  4. Ostm1 has a primary and autonomous role in neuronal homeostasis

  5. Omi (显示 HTRA2 ELISA试剂盒) is a recessive mutation in the Ostm1 gene affecting teeth and coat color.

  6. Ostm1 is a bona fide target of miR (显示 MLXIP ELISA试剂盒)-140, which is significantly decreased during adipogenic differentiation.

  7. Neuropathologic changes similar to neuronal ceroid lipofuscinosis (显示 CLN6 ELISA试剂盒) are found in osteoporosis associated transmembrane protein 1 (显示 TMEM1 ELISA试剂盒) (Ostml)-deficient mice.

  8. mutation induces severe malignant autosomal recessive osteopetrosis (显示 CSF1 ELISA试剂盒); studies show that Gl protein function is absolutely required for osteoclast and melanocyte maturation and function

  9. both ClC-7 (显示 CLCN7 ELISA试剂盒) and Ostm1 proteins co-localize in late endosomes and lysosomes of various tissues, as well as in the ruffled border of bone-resorbing osteoclasts

  10. microphthalmia transcription factor (显示 MITF ELISA试剂盒) regulates Clcn7 and Ostm1 expression in osteoclasts

OSTM1 抗原简介

Antigen Summary

This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis.

Gene names and symbols associated with OSTM1

  • osteopetrosis associated transmembrane protein 1 (OSTM1) 抗体
  • osteopetrosis associated transmembrane protein 1 (ostm1) 抗体
  • osteopetrosis associated transmembrane protein 1 (Ostm1) 抗体
  • osteopetrosis-associated transmembrane protein 1 (GL) 抗体
  • 1200002H13Rik 抗体
  • Gipn 抗体
  • gl 抗体
  • HSPC019 抗体
  • MGC145644 抗体
  • OPTB5 抗体
  • OSTM1 抗体
  • si:ch73-257c13.3 抗体

Protein level used designations for OSTM1

osteopetrosis-associated transmembrane protein 1 , osteopetrosis associated transmembrane protein 1 , GAIP-interacting protein N terminus , chloride channel 7 beta subunit , grey-lethal osteopetrosis , grey lethal osteopetrosis , GAIP interacting protein N terminus , osteopetrosis associated transmembrane protein 1-like

GENE ID SPECIES
421773 Gallus gallus
518522 Bos taurus
701341 Macaca mulatta
739203 Pan troglodytes
780037 Xenopus (Silurana) tropicalis
100137453 Papio anubis
100320445 Danio rerio
100328697 Oryctolagus cuniculus
28962 Homo sapiens
14628 Mus musculus
499474 Rattus norvegicus
100049681 Sus scrofa
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