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Invitrogen™ FANCM Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA5103839

Catalog No. PIPA5103839


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Description

Description

Antibody detects endogenous levels of total FANCM.

The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group M. Alternative splicing results in multiple transcript variants.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

FANCM
Polyclonal
Unconjugated
FANCM
AI427100; ATP-dependent RNA helicase FANCM; C730036B14Rik; D12Ertd364e; FAAP250; FANCM; Fanconi anemia complementation group M; Fanconi anemia group M protein; Fanconi anemia group M protein homolog; Fanconi anemia, complementation group M; fanconi anemia-associated polypeptide of 250 kDa; Kiaa1596; Protein FACM; Protein Hef ortholog; RGD1307897
Rabbit
Affinity chromatography
RUO
104806, 314172, 57697
-20°C
Liquid
Immunohistochemistry (Paraffin), Western Blot
1 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Q8BGE5, Q8IYD8
FANCM
A synthesized peptide derived from human FANCM(Accession Q8IYD8), corresponding to amino acid residues H447-S497.
100 μL
Primary
Human, Mouse, Rat
Antibody
IgG
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