Mouse anti-Human PQBP1 Monoclonal Antibody | anti-PQBP1 antibody

PQBP1 (Polyglutamine-binding Protein 1, PQBP-1, 38kD Nuclear Protein Containing a WW Domain, Npw38, Polyglutamine Tract-binding Protein 1, NPW38, JM26) (PE)

Cat. Num. AAA6159624

• Gene Names: PQBP1; SHS; MRX2; MRX55; MRXS3; MRXS8; NPW38; RENS1
• Reactivity: Human
• Applications: ELISA, Western Blot
• Purity: Purified by Protein A Affinity Chromatography.
• Synonyms: PQBP1; Monoclonal Antibody; PQBP1 (Polyglutamine-binding Protein 1; PQBP-1; 38kD Nuclear Protein Containing a WW Domain; Npw38; Polyglutamine Tract-binding Protein 1; NPW38; JM26) (PE); anti-PQBP1 antibody

• Host: Mouse
• Reactivity: Human
• Clonality: Monoclonal
• Isotype: IgG2a,k
• Clone Number: 1A11
• Specificity: Recognizes human PQBP1.
• Purity/Purification: Purified by Protein A Affinity Chromatography.
• Form/Format: Supplied as a liquid in PBS, pH 7.2. No preservative added. Labeled with R-Phycoerythrin (PE).
• Sequence Length: 1147

• Applicable Applications for anti-PQBP1 antibody: ELISA (EIA), Western Blot (WB)
• Application Notes: Applications are based on unconjugated antibody.
• Immunogen: Partial recombinant corresponding to aa184-265 from PQBP1 (NP_005701) with GST tag. MW of the GST tag alone is 26kD.
• Immunogen Sequence: LAPYPKSKKAVSRKDEELDPMDPSSYSDAPRGTWSTGLPKRNEAKTGADTTAAGPLFQQRPYPSPGAVLRANAEASRTKQQD
• Conjugate: PE
• Preparation and Storage: Store product at 4 degree C in the dark. DO NOT FREEZE! Stable at 4 degree C for 12 months after receipt as an undiluted liquid. Dilute required amount only prior to immediate use. Further dilutions can be made in assay buffer. Caution: PE conjugates are sensitive to light. For maximum recovery of product, centrifuge the original vial prior to removing the cap.

Western Blot (WB)

(Western Blot detection against Immunogen (34.76kD.)

Western Blot (WB)

(Western Blot analysis of PQBP1 expression in transfected 293T cell line by PQBP1 monoclonal antibodyLane 1: PQBP1 transfected lysate (30.5kD). Lane 2: Non-transfected lysate.)

Testing Data

(Detection limit for recombinant GST tagged PQBP1 is 0.3ng/ml as a capture antibody.)

Related Product Information for anti-PQBP1 antibody

May suppress the ability of POU3F2 to transactivate the DRD1 gene in a POU3F2 dependent manner. Can activate transcription directly or via association with the transcription machinery. May be involved in ATXN1 mutant-induced cell death. The interaction with ATXN1 mutant reduces levels of phosphorylated RNA polymerase II large subunit.

Product Categories/Family for anti-PQBP1 antibody

Antibodies; Proteins

NCBI and Uniprot Product Information

• NCBI GI #: 74027245
• NCBI GeneID: 10084
• NCBI Accession #: NM_005710.2
• NCBI GenBank Nucleotide #: NM_005710
• UniProt Accession #: O60828
• NCBI Official Full Name: Homo sapiens polyglutamine binding protein 1 (PQBP1), transcript variant 1, mRNA
• NCBI Official Synonym Full Names: polyglutamine binding protein 1
• NCBI Official Symbol: PQBP1
• NCBI Official Synonym Symbols: SHS; MRX2; MRX55; MRXS3; MRXS8; NPW38; RENS1
• NCBI Protein Information: polyglutamine-binding protein 1
• UniProt Protein Name: Polyglutamine-binding protein 1
• Protein Family: Polyglutamine-binding protein
• UniProt Gene Name: PQBP1
• UniProt Synonym Gene Names: NPW38; PQBP-1; Npw38
• UniProt Entry Name: PQBP1_HUMAN

NCBI Description

This gene encodes a nuclear polyglutamine-binding protein that is involved with transcription activation. The encoded protein contains a WW domain. Mutations in this gene have been found in patients with Renpenning syndrome 1 and other syndromes with X-linked cognitive disability. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.[provided by RefSeq, Nov 2009]

Uniprot Description

PQBP1: May suppress the ability of POU3F2 to transactivate the DRD1 gene in a POU3F2 dependent manner. Can activate transcription directly or via association with the transcription machinery. May be involved in ATXN1 mutant-induced cell death. The interaction with ATXN1 mutant reduces levels of phosphorylated RNA polymerase II large subunit. Defects in PQBP1 are the cause of Renpenning syndrome 1 (RENS1); also known as Sutherland-Haan X-linked mental retardation syndrome (SHS) or X-linked mental retardation syndromes MRXS3/MRXS8/MRX55. The clinical features are mental retardation, microcephaly, short stature, and small testes. The craniofacies tends to be narrow and tall with upslanting palpebral fissures, abnormal nasal configuration, cupped ears, and short philtrum. The nose may appear long or bulbous, with overhanging columella. Less consistent manifestations include ocular colobomas, cardiac malformations, cleft palate, and anal anomalies. RENS1 is more frequently in males than in females where little or no expression is found. 10 isoforms of the human protein are produced by alternative splicing.

Protein type: Transcription, coactivator/corepressor

Chromosomal Location of Human Ortholog: Xp11.23

Cellular Component: nucleoplasm; stress granule; cytoplasm; nuclear speck; nucleus

Molecular Function: ribonucleoprotein binding; DNA binding; transcription coactivator activity

Biological Process: alternative nuclear mRNA splicing, via spliceosome; transcription, DNA-dependent; regulation of transcription, DNA-dependent; regulation of RNA splicing; regulation of dendrite morphogenesis; neurite development

Disease: Renpenning Syndrome 1