catalog number :
MBS768988
products full name :
EML1 Rabbit Polyclonal
products short name :
[EML1]
products name syn :
[EML1, EMAP1, EMAP, ELP79, EMAPL1]
other names :
[echinoderm microtubule-associated protein-like 1 isoform a; Echinoderm microtubule-associated protein-like 1; echinoderm microtubule-associated protein-like 1; echinoderm microtubule associated protein like 1]
products gene name :
[EML1]
other gene names :
[EML1; EML1; EMAP; ELP79; EMAPL; HuEMAP; EMAP1; EMAPL; EMAPL1; EMAP-1; HuEMAP-1]
uniprot entry name :
EMAL1_HUMAN
specificity :
human, Mouse, rat; other species are not tested. Please decide the specificity by homology
purity :
Purity: >=95% as determined by SDS-PAGE. Purification: Immunogen Affinity Purified
storage stability :
-20°C for 24 months (Avoid repeated freeze / thaw cycles.)
tested application :
ELISA (EIA), Western Blot (WB), Immunofluorescence (IF)
app notes :
WB : 1:500-1:2000. IF : 1:10-1:100
image1 heading :
Immunofluorescent
image2 heading :
SDS-PAGE
other info1 :
. Calculated MW: 90kD . Immunogen: Echinoderm microtubule associated protein like 1
other info2 :
Buffer: PBS with 0.02% sodium azide and 50% glycerol pH 7.3
products description :
Modulates the assembly and organization of the microtubule cytoskeleton, and probably plays a role
in regulating the orientation of the mitotic spindle and the orientation of the plane of cell division.
Required for normal proliferation of neuronal progenitor cells in the developing brain and for normal
brain development. Does not affect neuron migration per se (By similarity).
ncbi acc num :
NP_001008707.1
ncbi gb acc num :
NM_001008707.1
ncbi summary :
Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
uniprot summary :
EML1: May modify the assembly dynamics of microtubules, such that microtubules are slightly longer, but more dynamic. Belongs to the WD repeat EMAP family. 2 isoforms of the human protein are produced by alternative splicing. Protein type: Microtubule-binding; Cytoskeletal. Chromosomal Location of Human Ortholog: 14q32. Cellular Component: cytosol; microtubule; microtubule associated complex; perinuclear region of cytoplasm. Molecular Function: calcium ion binding; microtubule binding; protein binding; tubulin binding. Biological Process: brain development; hemopoietic progenitor cell differentiation; microtubule cytoskeleton organization and biogenesis; mitotic spindle organization and biogenesis; neuroblast proliferation