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FANCM 产品

(Fanconi Anemia Complementation Group M (FANCM))

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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. [provided by RefSeq, Jul 2008].

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Featured FANCM Categories

FANCM 抗体

High quality antibodies with extensive validation data.

FANCM ELISA试剂盒

Reliable ELISA kits for a wide range of species.

Recommended FANCM 抗体

Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human, Mouse, Rat
Application WB, ELISA, IHC
Validations
  • (3)
Cat. No. ABIN6261677
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB, IF
Validations
  • (2)
Cat. No. ABIN528283
Quantity 50 μg
Datasheet Datasheet
Reactivity Human
Application WB
Validations
  • (1)
Cat. No. ABIN6242340
Quantity 200 μL
Datasheet Datasheet

Recommended FANCM ELISA试剂盒

Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Analytical Method
Validations
Cat. No. ABIN1132974
Quantity 96 tests
Datasheet Datasheet
Reactivity Mouse
Analytical Method
Validations
Cat. No. ABIN1132975
Quantity 96 tests
Datasheet Datasheet

Recommended FANCM 蛋白

Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Source Wheat germ
Validations
  • (1)
Cat. No. ABIN1353640
Quantity 10 μg
Datasheet Datasheet

Latest Publications for our FANCM Products

Fouquet, Pawlikowska, Caburet, Guigon, Mäkinen, Tanner, Hietala, Urbanska, Bellutti, Legois, Bessieres, Gougeon, Benachi, Livera, Rosselli, Veitia, Misrahi: "A homozygousFANCMmutation underlies a familial case of non-syndromic primary ovarian insufficiency." in: eLife, Vol. 6, (2018) (PubMed).

Kasak, Punab, Nagirnaja, Grigorova, Minajeva, Lopes, Punab, Aston, Carvalho, Laasik, Smith, Conrad, Laan: "Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia." in: American journal of human genetics, Vol. 103, Issue 2, pp. 200-212, (2018) (PubMed).

Barroso, Pita, Arias, Menendez, Zamora, Blanco, Benitez, Ribas: "The Fanconi anemia family of genes and its correlation with breast cancer susceptibility and breast cancer features." in: Breast cancer research and treatment, Vol. 118, Issue 3, pp. 655-60, (2009) (PubMed).

Synonyms and alternative names related to FANCM

Fanconi anemia complementation group M (FANCM), hypothetical protein (PGTG_17854), Fanconi anemia, complementation group M (Fancm), AI427100, C730036B14Rik, D12Ertd364e, FAAP250, KIAA1596

Protein level used designations for FANCM

  • Fanconi anemia complementation group M
  • fanconi anemia complementation group M
  • ATP-dependent RNA helicase FANCM
  • Fanconi anemia group M protein
  • fanconi anemia-associated polypeptide of 250 kDa
  • protein Hef ortholog
  • Fanconi anemia group M protein homolog
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