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anti-Human MAL Antibodies:
anti-Mouse (Murine) MAL Antibodies:
anti-Rat (Rattus) MAL Antibodies:
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Human Polyclonal MAL Primary Antibody for ELISA - ABIN451626
Khor, Chapman, Vannberg, Dunne, Murphy, Ling, Frodsham, Walley, Kyrieleis, Khan, Aucan, Segal, Moore, Knox, Campbell, Lienhardt, Scott, Aaby, Sow, Grignani, Sillah, Sirugo, Peshu, Williams, Maitland et al.: A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis. ... in Nature genetics 2007
Here the authors show that MAL TIR domains spontaneously and reversibly form filaments in vitro. They also form cofilaments with TLR4 (show TLR4 Antibodies) TIR domains and induce formation of MyD88 (show MYD88 Antibodies) assemblies.
MAL and TMEM220 were specifically methylated and were down-regulated in human gastric cancer.
Results show that MAl protein binds to and regulates MYD88 (show MYD88 Antibodies).
This study revealed that Merkel cell polyomavirus -negative Merkel cell carcinomas significantly expressed higher CADM1 and lower MAL than Merkel cell polyomavirus -positive Merkel cell carcinomas
CADM1/MAL methylation increases with severity of cervical intraepithelial neoplasia
Hypermethylation of the selected markers (MAL, PRIMA1, PTGDR (show PTGDR Antibodies) and SFRP1 (show SFRP1 Antibodies)) can result in reduced gene expression and may contribute to the formation of colorectal cancer.
Data suggest that expression of MAL in cells confers both ETX (Clostridium perfringens epsilon-toxin) binding and susceptibility to ETX-mediated cell death; cells expressing rat MAL are 100 times more sensitive to ETX than cells expressing human MAL.
The use of CADM1, MAL, and MIR124-2 as biomarkers for full molecular screening in HIV infected women who are also positive for human papillomavirus.
MAL is a critical element of the machinery for exosome secretion and may constitute a target for modulating exosome secretion by human T cells.
MAL hypermethylation is associated with esophageal carcinoma progression.
Expression of the developmentally regulated proteolipid MAL is required for the cytotoxic effect of Clostridium perfringens Epsilon Toxin.
MAL (show TIRAP Antibodies) overexpression leads to reduced expression of Mpz and p75NTR (show NGFR Antibodies), despite functional pathways and normal expression of genes important for Schwann cell differentiation.
the exclusion of MAL from the expanding 2D crystals of uroplakins explains the selective association of MAL with the hinge areas in the uroplakin-delivering fusiform vesicles, as well as at the apical surface
Phagosomal retention of Francisella tularensis results in TIRAP/Mal (show TIRAP Antibodies)-independent TLR2 (show TLR2 Antibodies) signaling.
The specific reduction and mistargeting of MAL protein as a reaction to sulfatide overload may contribute to the pathogenic mechanisms in metachromatic leukodystrophy.
Our results demonstrate a critical role for MAL in the maintenance of central nervous system paranodes, likely by controlling the trafficking and/or sorting of NF155 and other membrane components in oligodendrocytes.
Our results suggest a functional role for MAL in peripheral myelination by influencing the expression of membrane components that mediate axon-glia interaction during ensheathment and myelin wrapping.
SYP is an hexameric MAL-domain channel protein.
The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids. The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance of glycosphingolipid-enriched membrane microdomains. Down-regulation of this gene has been associated with a variety of human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence of alternatively spliced exons 2 and 3.
T-lymphocyte maturation-associated protein
, myelin and lymphocyte protein
, myelin and lymphocyte protein, T-cell differentiation protein
, Myelin and lymphocyte protein
, 17 kDa myelin vesicular protein
, NS 3
, VIP17 proteolipid
, VIP17/MAL proteolipid
, MAL-like protein