DCLRE1B Polyclonal Antibody

Background:
DCLRE1B (DNA Cross-Link Repair 1B) is a Protein Coding gene. Diseases associated with DCLRE1B include Hoyeraal Hreidarsson Syndrome and Dyskeratosis Congenita. Among its related pathways are Fanconi anemia pathway and DNA Double-Strand Break Repair. Gene Ontology (GO) annotations related to this gene include 5'-3' exonuclease activity. An important paralog of this gene is DCLRE1C.

Synonyms:
DCLRE1B, APOLLO, SNM1B, SNMIB

Immunogen: Recombinant fusion protein of human DCLRE1B (NP_073747.1).

Swissprot: Q9H816
Gene ID: 64858

Calculated MW: 60 kDa
Observed MW: 60 kDa

Purification Method: Affinity purification

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Concentration: 1 mg/mL
Dilution: "WB 1:500-1:2000"

Storage:
Store at -20°C. Avoid freeze / thaw cycles.