GNB1L antibody (AA 101-200) (AbBy Fluor® 594)

Catalog No. ABIN2813886

This Rabbit Polyclonal antibody specifically detects GNB1L in IF (cc) and IF (p). It exhibits reactivity toward Human.

Quick Overview for GNB1L antibody (AA 101-200) (AbBy Fluor® 594) (ABIN2813886)

Target: GNB1L (Guanine Nucleotide Binding Protein (G Protein), beta Polypeptide 1-Like (GNB1L))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GNB1L antibody is conjugated to AbBy Fluor® 594

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-GNB1L Antibody (AbBy Fluor® 594)

Binding Specificity: AA 101-200

Predicted Reactivity: Human,Mouse,Rat,Dog,Horse,Zebrafish

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GNB1L

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for GNB1L

Target: GNB1L (Guanine Nucleotide Binding Protein (G Protein), beta Polypeptide 1-Like (GNB1L))

Alternative Name: GNB1L

Background:

Synonyms: DGCRK3, ESTM55, fb98e06, fj09d12, FKSG1, G-protein beta subunit-like protein, guanine nucleotide binding protein G protein, beta polypeptide 1-like, guanine nucleotide binding protein beta-subunit-like polypeptide, GY2, KIAA1645, WDR14, WDVCF, wu:fb98e06, wu:fj09d12, zgc:55774.

Background: 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].

Gene ID: 54584