Catalog No.
YMK99901
Expression system
E. coli
Species
Mus musculus (Mouse)
Protein length
Asn57-Asn261
Predicted molecular weight
24.83 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P70407
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
Cadherin-9, Cdh9, T1-cadherin
Pleiotropy analysis between lobar intracerebral hemorrhage and CSF β-amyloid highlights new and established associations., PMID:36705426
Clinicopathologic and Molecular Study of Hybrid Nerve Sheath Tumors Reveals Their Common Association With Fusions Involving VGLL3., PMID:35256555
Association of CDH11 with Autism Spectrum Disorder Revealed by Matched-gene Co-expression Analysis and Mouse Behavioral Studies., PMID:34523068
Mutations of METTL3 predict response to neoadjuvant chemotherapy in muscle-invasive bladder cancer., PMID:34239995
Investigation of Association of Rare, Functional Genetic Variants With Heavy Drinking and Problem Drinking in Exome Sequenced UK Biobank Participants., PMID:33893496
MiR-22-3p Suppresses Vascular Remodeling and Oxidative Stress by Targeting CHD9 during the Development of Hypertension., PMID:33794525
Transcriptomic analysis reveals the molecular mechanism of Alzheimer-related neuropathology induced by sevoflurane in mice., PMID:31134678
Segregated expressions of autism risk genes Cdh11 and Cdh9 in autism-relevant regions of developing cerebellum., PMID:31046797
Cadherin Combinations Recruit Dendrites of Distinct Retinal Neurons to a Shared Interneuronal Scaffold., PMID:30197236
A signal-based method for finding driver modules of breast cancer metastasis to the lung., PMID:28855549
Infertility diagnosis has a significant impact on the transcriptome of developing blastocysts., PMID:28595284
Breathing control center neurons that promote arousal in mice., PMID:28360327
Brain enhancer activities at the gene-poor 5p14.1 autism-associated locus., PMID:27503586
Polygenic associations of neurodevelopmental genes in suicide attempt., PMID:26666204
Association between genetic variants related to glutamatergic, dopaminergic and neurodevelopment pathways and white matter microstructure in child and adolescent patients with obsessive-compulsive disorder., PMID:26254621
Complex and dynamic expression of cadherins in the embryonic marmoset cerebral cortex., PMID:26081465
Type II cadherins guide assembly of a direction-selective retinal circuit., PMID:25126785
Sp1-mediated microRNA-182 expression regulates lung cancer progression., PMID:24519909
Pemphigus vulgaris autoantibody profiling by proteomic technique., PMID:23505434
Morphology of renal interstitial fibroblasts., PMID:22952092
Analysis of four genes involved in the neurodevelopment shows association of rs4307059 polymorphism in the cadherin 9/10 region with completed suicide., PMID:22846907
Cadherins and neuropsychiatric disorders., PMID:22765916
PP065. dNK and dNK-CM mediated alterations of DNA methylation in extravillous cytotrophoblasts (EVTS)., PMID:26105388
Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism., PMID:22738016
Characterization of Epstein-Barr virus (EBV) BZLF1 gene promoter variants and comparison of cellular gene expression profiles in Japanese patients with infectious mononucleosis, chronic active EBV infection, and EBV-associated hemophagocytic lymphohistiocytosis., PMID:22511310
Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation., PMID:21426945
A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa., PMID:21079607
Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex., PMID:20615956
Common genetic variants on 5p14.1 associate with autism spectrum disorders., PMID:19404256
Cadherin-9 is a novel cell surface marker for the heterogeneous pool of renal fibroblasts., PMID:17668045
Identification of three human type-II classic cadherins and frequent heterophilic interactions between different subclasses of type-II classic cadherins., PMID:10861224