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FANCM Rabbit anti-Human, Polyclonal, Bioss
SDP

Rabbit Polyclonal Antibody

Supplier:  Bioss BS13143R

Encompass_Preferred

Catalog No. 50-198-2648


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Description

Description

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.
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
Protein A
RUO
57697
-20°C
Liquid
Immunofluorescence, Immunohistochemistry (Paraffin)
1 μg/mL
PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Q8IYD8
FANCM
KLH conjugated synthetic peptide derived from human FANCM.
100 μL
Primary
Human
Antibody
IgG
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