Products for Research Use Only

MCM2 Rabbit Polyclonal Antibody (APC)

CAT: 0013-GTR18528821Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18528821Size:100 µg
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Description
MCM2 Rabbit Polyclonal Antibody (APC)
Product Name Alternative
DNA replication licensing factor MCM2; 3.6.4.12; Minichromosome maintenance protein 2 homolog; Nuclear protein BM28; MCM2; BM28, CCNL1, CDCL1, KIAA0030
UniProt
P49736
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins
Immunogen
A synthetic peptide corresponding to a sequence at the C-terminus of human MCM2, different from the related rat and mouse sequences by two amino acids.
Target
DNA replication licensing factor MCM2
Clonality
Polyclonal
Conjugation
APC
Field of Research
Epigenetics & Chromatin, Molecular Biology
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Molecular Weight
101896 Da
Storage Conditions
At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
Notes
For research use only.
Applications Notes
Recommended applications are based on the parent unconjugated antibody. Customers may select suitable applications according to their experimental needs.
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Isotype
Rabbit IgG

UniProtKB · P49736

DNA replication licensing factor MCM2

MCM2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P49736
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
MCM2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
3.6.4.12
Processing
—
Secondary accessions
Q14577, Q15023, Q8N2V1, Q969W7, Q96AE1, Q9BRM7
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationIsopeptide bondPhosphoproteinUbl conjugation

Ligand

ATP-bindingMetal-bindingNucleotide-bindingZinc

Biological process

Cell cycleDNA replication

Cellular component

ChromosomeNucleus

Disease

DeafnessDisease variantNon-syndromic deafness

Molecular function

DNA-bindingHelicaseHydrolase

Domain

Zinc-finger