多克隆抗体

PHF11 rabbit Polyclonal Antibody

PHF11抗体
PHF11抗体应用:WB 1:500-2000 This gene encodes a protein containing a PHD (plant homeodomain) type zinc finger. This gene has been identified in some studies as a candidate gene for asthma. Naturally-occurring readthrough transcription may occur from the upstream SETDB2 (SET domain bifurcated 2) gene to this locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016],

PHF6 rabbit Polyclonal Antibody

PHF6抗体
PHF6抗体应用:WB 1:500-2000 ELISA 1:5000-20000PHD finger protein 6(PHF6) Homo sapiens This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by mental retardation, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [provided by RefSeq, Jun 2010],

PHLB3 rabbit Polyclonal Antibody

PHLB3抗体
PHLB3抗体应用:WB 1:500-2000

PHLD rabbit Polyclonal Antibody

PHLD抗体
PHLD抗体应用:WB 1:500-2000 ELISA 1:5000-20000glycosylphosphatidylinositol specific phospholipase D1(GPLD1) Homo sapiens Many proteins are tethered to the extracellular face of eukaryotic plasma membranes by a glycosylphosphatidylinositol (GPI) anchor. The GPI-anchor is a glycolipid found on many blood cells. The protein encoded by this gene is a GPI degrading enzyme. Glycosylphosphatidylinositol specific phospholipase D1 hydrolyzes the inositol phosphate linkage in proteins anchored by phosphatidylinositol glycans, thereby releasing the attached protein from the plasma membrane. [provided by RefSeq, Jul 2008],

PHLP rabbit Polyclonal Antibody

PHLP抗体
PHLP抗体应用:WB 1:500-2000 Phosducin-like protein is a putative modulator of heterotrimeric G proteins. The protein shares extensive amino acid sequence homology with phosducin, a phosphoprotein expressed in retina and pineal gland. Both phosducin-like protein and phosphoducin have been shown to regulate G-protein signaling by binding to the beta-gamma subunits of G proteins. [provided by RefSeq, Jul 2008],

PHLP1 rabbit Polyclonal Antibody

PHLP1抗体
PHLP1抗体应用:WB 1:500-2000 ELISA 1:5000-20000PH domain and leucine rich repeat protein phosphatase 1(PHLPP1) Homo sapiens This gene encodes a member of the serine/threonine phosphatase family. The encoded protein promotes apoptosis by dephosphorylating and inactivating the serine/threonine kinase Akt, and functions as a tumor suppressor in multiple types of cancer. Increased expression of this gene may also play a role in obesity and type 2 diabetes by interfering with Akt-mediated insulin signaling. [provided by RefSeq, Dec 2011],

PHTF1 rabbit Polyclonal Antibody

PHTF1抗体
PHTF1抗体应用:WB 1:500-2000

PHX2A rabbit Polyclonal Antibody

PHX2A抗体
PHX2A抗体应用:WB 1:500-2000 ELISA 1:5000-20000paired like homeobox 2a(PHOX2A) Homo sapiens The protein encoded by this gene contains a paired-like homeodomain most similar to that of the Drosophila aristaless gene product. The encoded protein plays a central role in development of the autonomic nervous system. It regulates the expression of tyrosine hydroxylase and dopamine beta-hydroxylase, two catecholaminergic biosynthetic enzymes essential for the differentiation and maintenance of the noradrenergic neurotransmitter phenotype. The encoded protein has also been shown to regulate transcription of the alpha3 nicotinic acetylcholine receptor gene. Mutations in this gene have been associated with autosomal recessive congenital fibrosis of the extraocular muscles. [provided by RefSeq, Jul 2008],

PHX2B rabbit Polyclonal Antibody

PHX2B抗体
PHX2B抗体应用:WB 1:500-2000 ELISA 1:5000-20000paired like homeobox 2b(PHOX2B) Homo sapiens The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins localized to the nucleus. The protein functions as a transcription factor involved in the development of several major noradrenergic neuron populations and the determination of neurotransmitter phenotype. The gene product is linked to enhancement of second messenger-mediated activation of the dopamine beta-hydroylase, c-fos promoters and several enhancers, including cyclic amp-response element and serum-response element. Expansion of a 20 amino acid polyalanine tract in this protein by 5-13 aa has been associated with congenital central hypoventilation syndrome. [provided by RefSeq, Jul 2016],

PI16 rabbit Polyclonal Antibody

PI16抗体
PI16抗体应用:WB 1:500-2000 ELISA 1:5000-20000function:Putative serine protease inhibitor.,miscellaneous:May serve as a marker following prostatectomy for prostate cancer.,PTM:N-glycosylated.,similarity:Belongs to the CRISP family.,subunit:Interacts with PSP94/MSMB.,tissue specificity:Expressed in prostate, testis, ovary and intestine. Concentrates in prostate cencer patient's sera.,
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