Products for Research Use Only

MCM2 Rabbit Polyclonal Antibody (Biotin)

CAT: 0013-GTR18528826Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18528826Size:100 µg
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Description
MCM2 Rabbit Polyclonal Antibody (Biotin)
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
Biotin
Field of Research
Epigenetics & Chromatin, Molecular Biology
Purification
Immunogen affinity purified.
Dilution
Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, 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.
Notes
For research use only.
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