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抗Rat (Rattus) SALL4 抗体:
抗Mouse (Murine) SALL4 抗体:
抗Human SALL4 抗体:
Human Monoclonal SALL4 Primary Antibody for IHC (p), ELISA - ABIN566099
Cauffman, De Rycke, Sermon, Liebaers, Van de Velde: Markers that define stemness in ESC are unable to identify the totipotent cells in human preimplantation embryos. in Human reproduction (Oxford, England) 2008
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Human Polyclonal SALL4 Primary Antibody for ELISA, WB - ABIN4369825
Paradisi, Arias: IVIC syndrome is caused by a c.2607delA mutation in the SALL4 locus. in American journal of medical genetics. Part A 2007
Show all 3 Pubmed References
Human Polyclonal SALL4 Primary Antibody for WB - ABIN388303
Yang, Chai, Liu, Fink, Lin, Silberstein, Amin, Ward, Ma: Bmi-1 is a target gene for SALL4 in hematopoietic and leukemic cells. in Proceedings of the National Academy of Sciences of the United States of America 2007
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Rat (Rattus) Polyclonal SALL4 Primary Antibody for ELISA, WB - ABIN253101
Wang, Rao, Chu, Shen, Levasseur, Theunissen, Orkin: A protein interaction network for pluripotency of embryonic stem cells. in Nature 2006
Data show that both sall1 (显示 SALL1 抗体) and sall4 act to repress pou5f3 (oct4)family gene expression in the neural plate, thereby allowing vertebrate neural development to proceed.
These results suggest that Sall4, activated by posteriorizing signals, represses the pou5f3 genes to provide a permissive environment.
SAL family member (XlSALL4) is expressed at the right place and time to play a role regulating both digit identity along the anterior/posterior axis and epimorphic limb regeneration
Sall4 expression expression in chemosensory cells implicates this transcription factor in the development and renewal of taste epithelia in zebrafish.
Sall gene family redundancy and tbx5 (显示 TBX5 抗体) offer explanations for the similarity of individuals with Okihiro syndrome and Holt-Oram syndrome limb defects
Findings indicate that SALL4 critically contributes to MLL (显示 MLL 抗体)-AF9 (显示 MLLT3 抗体)-induced leukemia, unraveling the underlying transcriptional and epigenetic mechanisms in this disease.
SALL4 associated with the NuRD co-repressor and repressed expression of the tumor suppressor genes Foxl1 (显示 FOXL1 抗体) and Dusp4 (显示 DUSP9 抗体).
Study propose a model whereby enhancer binding by Sall4 and other pluripotency-associated transcription factors is responsible for maintaining the balance between transcriptional programmes in pluripotent cells.
SALL4 has a negative impact in DNA damage repair, and support the model of dual functional properties of SALL4 in leukemogenesis through inhibiting DNA damage repair and promoting cell survival.
these data reveal the full profile of PLZF (显示 ZBTB16 抗体) and SALL4 regulatory targets in undifferentiated spermatogonia.
study explores a pivotal role of Sall4 in regulating epigenetic maturation of mouse oocytes.
JARID2 (显示 JARID2 抗体) physically interacts with ESRRB (显示 ESRRB 抗体), SALL4A, and PRDM14 (显示 PRDM14 抗体)
As SALL4A is known to impair ZBTB16 (显示 ZBTB16 抗体)-mediated Kit repression , our study provides novel insights into the molecular mechanism by which ATRA could control KIT expression, and thereby the differentiation of Aal into A1 spermatogonia in vivo.
In differentiated ESCs (显示 NR2E3 抗体), Sall4 bound to these somatic cell program gene loci, which are reportedly occupied by Prdm1 (显示 PRDM1 抗体) in embryonic carcinoma cells.
This study identified a critical role of the Sall4-Gli3 (显示 GLI3 抗体) system at the early steps of limb development for proper development of the appendicular skeletal elements.
These data indicate that aberrantly expressed SALL4 in human choriocarcinoma cells may promote cell proliferation via beta-catenin (显示 CTNNB1 抗体)/c-Myc (显示 MYC 抗体) pathway
SALL4 was significantly upregulated in glioma tissues and cell lines, and an inverse correlation between miR (显示 MLXIP 抗体)-98 and SALL4 expression in glioma tissues was identified.
TNFSF13 (显示 TNFSF13 抗体), SPATC1L, SLC22A25 (显示 SLC22A25 抗体) and SALL4 may thus be novel susceptibility loci for atrial fibrillation in the Japanese population
Study showed significantly high expression of SALL4 mRNA in glioma specimens as compared to non-tumor samples using RT-PCR. Blocking SALL4 using SALL4-siRNA decreased proliferation of U87 and U251 cells, which was reversed by the addition of PTEN inhibitor phen (bpv). Furthermore, marked increase in PTEN mRNA and protein levels was seen in cells treated with siRNA-SALL4.
SALL4 is a promising prognostic biomarker for cancer, and is appropriate for the assessment of cancer prognosis in the Chinese people.
Our experimental data indicated that over expression of SALL4 was found in CRC (显示 CALR 抗体) and low expression of SALL4 was connected with high survival rate after surgery. Thus our study suggested that SALL4 could serve as a potential diagnostic and prognostic marker of CRC (显示 CALR 抗体).
SALL4 is a target gene of miR (显示 MLXIP 抗体)-181b in glioma.SALL4 is upregulated in glioma.
SALL4 is a target gene of mir (显示 MLXIP 抗体)-98 in non-small cell lung cancer cells.
miR (显示 MLXIP 抗体)-98 plays a suppressive role in the proliferation, migration, invasion and EMT (显示 ITK 抗体) of HCC (显示 FAM126A 抗体) cells, partly at least, via directly inhibition of SALL4.
SALL4 immunopositivity is not a prognostic factor in Combined hepatocellular carcinoma (HCC (显示 FAM126A 抗体)) and cholangiocarcinoma (CC) (cHCC-CC); however, it is associated with alpha-fetoprotein (显示 AFP 抗体), glypican 3 (显示 GPC3 抗体) and EpCAM (显示 EPCAM 抗体) immunopositivity, indicating the mechanism of carcinogenesis.
The protein encoded by this gene may be a zinc finger transcription factor. Defects in this gene are a cause of Duane-radial ray syndrome (DRRS).
sal-like 4 (Drosophila)
, sal-like protein 4-like
, sal-like 4
, zinc finger transcription factor SALL4 a
, sal-like protein 4
, zinc finger protein SALL4
, zinc finger protein 797