FANCG antibody (AA 343-622)

Catalog No. ABIN6140474

Product Details anti-FANCG Antibody

Target: FANCG (Fanconi Anemia Complementation Group G (FANCG))

Binding Specificity: AA 343-622

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FANCG antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: QSQTKHILAS RCLQTGRAGD AAEHYLDLLA LLLDSSEPRF SPPPSPPGPC MPEVFLEAAV ALIQAGRAQD ALTLCEELLS RTSSLLPKMS RLWEDARKGT KELPYCPLWV SATHLLQGQA WVQLGAQKVA ISEFSRCLEL LFRATPEEKE QGAAFNCEQG CKSDAALQQL RAAALISRGL EWVASGQDTK ALQDFLLSVQ MCPGNRDTYF HLLQTLKRLD RRDEATALWW RLEAQTKGSH EDALWSLPLY LESYLSWIRP SDRDAFLEEF RTSLPKSCDL

Cross-Reactivity: Human, Mouse

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 343-622 of human FANCG (NP_004620.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

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

Target Details for FANCG

Target: FANCG (Fanconi Anemia Complementation Group G (FANCG))

Alternative Name: FANCG (FANCG Products)

Synonyms: xFANCG antibody, FAG antibody, XRCC9 antibody, AU041407 antibody, Xrcc9 antibody, Fanconi anemia complementation group G S homeolog antibody, Fanconi anemia complementation group G antibody, Fanconi anemia, complementation group G antibody, fancg.S antibody, FANCG antibody, Fancg antibody

Background: 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 G.,FANCG,FAG,XRCC9,Epigenetics & Nuclear Signaling,DNA Damage & Repair,FANCG

Molecular Weight: 68 kDa

Gene ID: 2189

UniProt: O15287

Pathways: DNA Damage Repair