ARG45306

anti-RNase H1 / RNH1 antibody

anti-RNase H1 / RNH1 antibody for Flow cytometry,ICC/IF,Western blot and Human,Mouse

Overview

Product Description Polyclonal antibody recognizes RNase H1 / RNH1
Tested Reactivity Hu, Ms
Tested Application FACS, ICC/IF, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name RNase H1 / RNH1
Antigen Species Human
Immunogen Recombinant protein containing to human RNase H1 / RNH1.
Conjugation Un-conjugated
Alternate Names RNASEH1; Ribonuclease H1; Ribonuclease H Type II; RNase H1; RNH1; EC 3.1.26.4; H1RNA; PEOB2

Application Instructions

Application Suggestion
Tested Application Dilution
FACS1 - 3 µg/10^6 cells
ICC/IF5 μg/ml
WB0.25-0.5 μg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 38 kDa

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer 0.2% Na2HPO4, 0.9% NaCl and 4% Trehalose.
Stabilizer 4% Trehalose
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 246243 Human RNASEH1

Swiss-port # O60930 Human Ribonuclease H1

Gene Symbol RNASEH1
Gene Full Name Ribonuclease H1
Background This gene encodes an endonuclease that specifically degrades the RNA of RNA-DNA hybrids and plays a key role in DNA replication and repair. Alternate in-frame start codon initiation results in the production of alternate isoforms that are directed to the mitochondria or to the nucleus. The production of the mitochondrial isoform is modulated by an upstream open reading frame (uORF). Mutations in this gene have been found in individuals with progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2. Alternative splicing results in additional coding and non-coding transcript variants. Pseudogenes of this gene have been defined on chromosomes 2 and 17. [provided by RefSeq, Jul 2017]
Function Endonuclease that specifically degrades the RNA of RNA-DNA hybrids. [UniProt]
Cellular Localization Cytoplasm. [UniProt]
Calculated MW 32 kDa