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anti-Human COL11A1 Antikörper:
anti-Mouse (Murine) COL11A1 Antikörper:
anti-Rat (Rattus) COL11A1 Antikörper:
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Mouse (Murine) Polyclonal COL11A1 Primary Antibody für WB - ABIN4895101
Seet, Toh, Chu, Finger, Chua, Wong: Upregulation of distinct collagen transcripts in post-surgery scar tissue: a study of conjunctival fibrosis. in Disease models & mechanisms 2017
In this study, three novel and two known mutations in the COL2A1 (zeige COL2A1 Antikörper) gene were identified in six of 16 Chinese patients with Stickler syndrome. This is the first study in a cohort of Chinese patients with Stickler syndrome, and the results expand the mutation spectrum of the COL2A1 (zeige COL2A1 Antikörper) gene.
Chondrogenic potential was higher and Wnt (zeige WNT2 Antikörper)/beta-catenin (zeige CTNNB1 Antikörper) signaling was more potently activated by a GSK-3beta (zeige GSK3b Antikörper) inhibitor in the posterior than in the anterior part of the human infant sclera.
genetic variants of COL11A1 contribute to adult height in Chinese Han population but not to children height
proCOL11A1, fibroblast-activated protein, secreted protein acidic and rich in cysteine (zeige SPARC Antikörper), and periostin (zeige POSTN Antikörper) expression was significantly increased in the intratumoral stroma of pancreatic ductal adenocarcinomas compared to paired non-neoplastic pancreata
we demonstrate how COL11A1 regulates twist family basic helix-loop-helix transcription factor (zeige HEY1 Antikörper) 1 (zeige HNF1A Antikörper)-related protein 1 (TWIST1 (zeige TWIST1 Antikörper)) to induce chemoresistance and inhibit apoptosis in ovarian cancer cells
the racial differences of COL11A1 were consistent across multiple molecular levels, with higher mutation frequency, higher methylation, and lower expression in White patients. This indicated that COL11A1 might play important roles in ESCC, especially in White population. Additional studies are needed to further explore their functions in esophageal cancer
Investigated genetic variants in COL11A1 predisposing to primary hip OA in Han Chinese individuals.Two SNPs (rs1241164 and rs4907986) were found to be significantly associated with hip OA risk (adjusted p = 0.000731 and 0.000477). An increased risk of OA was associated with possession of the C allele of rs1241164 and the T allele of rs4907986.
COL11A1 antibody can assist in distinguishing the cancer-associated desmoplastic stroma from that associated with misplaced adenomatous mucosa. It is particularly helpful when electrocautery artifacts or mucin (zeige SLC13A2 Antikörper) pools interfere with the diagnosis of invasive carcinoma. However, COL11A1 has limited value in diagnosing superfically invasive carcinomas with very little desmoplastic stroma.
COL11A1 is overexpressed in gastric cancer tissues and regulates cell proliferation and migration.
COL11A1 may sever as a biomarker for metastatic NSCLC.
Taken together, these results indicate that the transcription factor Sp1 (zeige SP1 Antikörper) upregulates the proximal promoter activity of the mouse Col11a1 gene in chondrocytes.
these results indicate that the transcription factor NF-Y regulates the proximal promoter activity of mouse Col11a1 gene in chondrocytes
Stickler syndrome and Marshall syndrome mutations in COL11A1 cause hearing loss via dominant negative effects upon wild-type fibrillar collagen polypeptides in the extracellular matrices of the cochlea.
the cho mutation leads to osteoarthritis through a mechanism that does not initially involve mechanical factors.
The expression patterns suggest essential roles for Col11a1 and Col11a2 (zeige COL11A2 Antikörper) in the basilar or tectorial membranes.
Lef1 (zeige LEF1 Antikörper) is an activator of the Col11a1 promoter and that Col11a1 suppresses terminal osteoblast differentiation
This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Mutations in this gene are associated with type II Stickler syndrome and with Marshall syndrome. A single-nucleotide polymorphism in this gene is also associated with susceptibility to lumbar disc herniation. Multiple transcript variants have been identified for this gene.
alpha 1 type XI collagen
, collagen alpha-1(XI) chain
, collagen type XI alpha-1a
, collagen alpha-3(V) chain
, collagen, type XI, alpha 1
, collagen alpha-1(XI) chain-like
, collagen XI, alpha-1 polypeptide
, a1(XI) collagen
, pro-alpha1(XI) collagen
, procollagen, type XI, alpha 1
, collagen type XI
, collagen type a1(XI)6A-7-8
, collagen type a1(XI)6B-7
, procollagen type XI alpha 1