ALS抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/10000.insulin like growth factor binding protein acid labile subunit(IGFALS) Homo sapiens The protein encoded by this gene is a serum protein that binds insulin-like growth factors, increasing their half-life and their vascular localization. Production of the encoded protein, which contains twenty leucine-rich repeats, is stimulated by growth hormone. Defects in this gene are a cause of acid-labile subunit deficiency, which maifests itself in a delayed and slow puberty. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Mar 2009],

ALS2CR11抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/40000.amyotrophic lateral sclerosis 2 chromosome region candidate 11(ALS2CR11) Homo sapiens An autosomal recessive form of juvenile amyotrophic lateral sclerosis was originally mapped to a region of chromosome 2 that includes this gene. The encoded protein contains a calcium-dependent membrane targeting C2 domain. This domain is often found in proteins that are involved in membrane trafficking and signal transduction. [provided by RefSeq, Jun 2016],

ALS2CR13抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/5000.miscellaneous:ALS2CR13 is mapped in the genomic region covering the complete candidate region for Amyotrophic lateral sclerosis 2 (ALS2).,sequence caution:Contaminating sequence. Sequence of unknown origin in the N-terminal part.,

ALS2CR4抗体应用：WB 1:500-2000 ELISA 1:5000-20000transmembrane protein 237(TMEM237) Homo sapiens The protein encoded by this gene is a tetraspanin protein that is thought to be involved in WNT signaling. Defects in this gene are a cause of Joubert syndrome-14. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012],

ALS2CR7抗体应用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/10000.CDK15 (Cyclin-Dependent Kinase 15) is a Protein Coding gene. Diseases associated with CDK15 include amyotrophic lateral sclerosis 2, juvenile. GO annotations related to this gene include transferase activity, transferring phosphorus-containing groups and protein tyrosine kinase activity. An important paralog of this gene is CDK14.

ALS2CR8抗体应用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000.function:May be a transcription factor.,

ALX3抗体应用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000.ALX homeobox 3(ALX3) Homo sapiens This gene encodes a nuclear protein with a homeobox DNA-binding domain that functions as a transcriptional regulator involved in cell-type differentiation and development. Preferential methylation of this gene's promoter is associated with advanced-stage neuroblastoma tumors. [provided by RefSeq, Jul 2008],

ALY抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/10000.Aly/REF export factor(ALYREF) Homo sapiens The protein encoded by this gene is a heat stable, nuclear protein and functions as a molecular chaperone. It is thought to regulate dimerization, DNA binding, and transcriptional activity of basic region-leucine zipper (bZIP) proteins. [provided by RefSeq, Jul 2008],

AMBRA1抗体应用：WB 1:500-2000, ELISA 1:10000-20000function:Regulates autophagy and development of the nervous system. Involved in autophagy in controlling protein turnover during neuronal development, and in regulating normal cell survival and proliferation.,similarity:Contains 3 WD repeats.,subunit:Interacts with BECN1. Probably forms a complex with BECN1 and PIK3C3.,

Ameloblastin抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/10000.ameloblastin(AMBN) Homo sapiens This gene encodes the nonamelogenin enamel matrix protein ameloblastin. The encoded protein may be important in enamel matrix formation and mineralization. This gene is located in the calcium-binding phosphoprotein gene cluster on chromosome 4. Mutations in this gene may be associated with dentinogenesis imperfect and autosomal dominant amylogenesis imperfect. [provided by RefSeq, Aug 2011],