Rabbit anti-Human GNB1L Polyclonal Antibody | anti-GNB1L antibody

GNB1L Antibody

Cat. Num. AAA9430079

• Gene Names: GNB1L; GY2; FKSG1; WDR14; WDVCF; DGCRK3
• Reactivity: Human
• Applications: Immunohistochemistry
• Purity: Antigen affinity purification
• Synonyms: GNB1L; Polyclonal Antibody; GNB1L Antibody; GY2; FKSG1; WDR14; WDVCF; DGCRK3; anti-GNB1L antibody

• Host: Rabbit
• Reactivity: Human
• Clonality: Polyclonal
• Isotype: IgG
• Specificity: The antibody detects endogenous levels of total GNB1L protein.
• Purity/Purification: Antigen affinity purification
• Form/Format: In pH7.4 PBS, 0.05% NaN3, 40% Glycerol.
• Concentration: 1mg/ml (varies by lot)
• Sequence Length: 327

• Applicable Applications for anti-GNB1L antibody: Immunohistochemistry (IHC)
• Application Notes: IF: 1: 20-100
• Immunogen: Synthetic peptide of human GNB1L
• Immunogen Type: Peptide
• Preparation and Storage: Store at -20 degree C.

Immunohistochemistry (IHC)

(The image is immunohistochemistry of paraffin-embedded Human brain tissue using 47049(DGCR6 Antibody) at dilution 1/20. (Original magnification: 200))

Related Product Information for anti-GNB1L antibody

This gene encodes a G-protein beta-subunit-like polypeptide which is a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene.

Product Categories/Family for anti-GNB1L antibody

Total protein Ab

NCBI and Uniprot Product Information

• NCBI GI #: 17402902
• NCBI GeneID: 54584
• NCBI Accession #: NP_443730
• NCBI GenBank Nucleotide #: NM_053004.2
• UniProt Accession #: Q9BYB4; Q9H2S2; Q9H4M4
• Molecular Weight: 22,896 Da
• NCBI Official Full Name: guanine nucleotide-binding protein subunit beta-like protein 1
• NCBI Official Synonym Full Names: G protein subunit beta 1 like
• NCBI Official Symbol: GNB1L
• NCBI Official Synonym Symbols: GY2; FKSG1; WDR14; WDVCF; DGCRK3
• NCBI Protein Information: guanine nucleotide-binding protein subunit beta-like protein 1
• UniProt Protein Name: Guanine nucleotide-binding protein subunit beta-like protein 1
• Protein Family: Guanine nucleotide-binding protein subunit beta-like protein
• UniProt Gene Name: GNB1L
• UniProt Synonym Gene Names: GY2; KIAA1645; WDR14; G protein subunit beta-like protein 1; WDVCF

NCBI Description

This gene encodes a G-protein beta-subunit-like polypeptide which is a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene. [provided by RefSeq, Jul 2008]