Human Fanconi anemia group D2 protein, FANCD2 ELISA Kit | MyBioSource MBS9334438 product information

product summary

company name :

MyBioSource

product type :

ELISA/assay

product name :

Human Fanconi anemia group D2 protein, FANCD2 ELISA Kit

catalog :

MBS9334438

quantity :

48-Strip-Wells

price :

470 USD

more info or order :

MyBioSource product webpage

product information

catalog number :

MBS9334438

products type :

ELISA Kit

products full name :

Human Fanconi anemia group D2 protein, FANCD2 ELISA Kit

products short name :

[Fanconi anemia, complementation group D2]

products name syn :

[Human Fanconi anemia group D2 protein (FANCD2) ELISA kit; DKFZp762A223; FA-D2; FA4; FACD; FAD; FAD2; FANCD; FLJ23826; Fanconi anemia complementation group D2; OTTHUMP00000207925; type 4 Fanconi pancytopenia; Fanconi anemia; complementation group D2]

other names :

[Fanconi anemia group D2 protein isoform b; Fanconi anemia group D2 protein; Fanconi anemia group D2 protein; Fanconi anemia, complementation group D2]

products gene name :

[FANCD2]

other gene names :

[FANCD2; FANCD2; FA4; FAD; FACD; FAD2; FA-D2; FANCD; FACD; Protein FACD2]

uniprot entry name :

FACD2_HUMAN

reactivity :

Human

specificity :

No significant cross-reactivity or interference between this analyte and analogues is observed.

storage stability :

Store all reagents at 2-8 degree C

other info1 :

Assay Type: Quantitative Sandwich. Detection Range: 3.12 ng/ml - 100 ng/ml. Sensitivity: 1.0 ng/ml.

other info2 :

Intra-assay Precision: Intra-assay CV (%) is less than 15%. Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100].

products description :

Background: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic or diagnostic applications! This kit is intended to be used for determination the level of FANCD2 (hereafter termed "analyte") in undiluted original Human body fluids, tissue homogenates, secretions or feces samples. This kit is NOT suitable for assaying non-biological sources of substances.

ncbi gi num :

66528888

ncbi acc num :

NP_001018125.1

ncbi gb acc num :

NM_001018115.1

uniprot acc num :

Q9BXW9

ncbi mol weight :

166,462 Da

ncbi pathways :

BARD1 Signaling Events Pathway (137959); DNA Repair Pathway (105837); DNA Damage Response Pathway (198788); Fanconi Anemia Pathway (105895); Fanconi Anemia Pathway (377262); Fanconi Anemia Pathway (377128); Regulation Of The Fanconi Anemia Pathway (105896); TNF-alpha/NF-kB Signaling Pathway (198884)

ncbi summary :

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 D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA1 AND BRCA2) involved in homology-directed DNA repair. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

uniprot summary :

FANCD2: Required for maintenance of chromosomal stability. Promotes accurate and efficient pairing of homologs during meiosis. Involved in the repair of DNA double-strand breaks, both by homologous recombination and single-strand annealing. May participate in S phase and G2 phase checkpoint activation upon DNA damage. Plays a role in preventing breakage and loss of missegregating chromatin at the end of cell division, particularly after replication stress. Required for the targeting, or stabilization, of BLM to non-centromeric abnormal structures induced by replicative stress. Promotes BRCA2/FANCD1 loading onto damaged chromatin. May also be involved in B-cell immunoglobulin isotype switching. Interacts directly with FANCE and FANCI. Interacts with USP1 and MEN1. The ubiquitinated form specifically interacts with BRCA1 and BLM. Both the nonubiquitinated and the monoubiquitinated forms interact with BRCA2; this interaction is mediated by phosphorylated FANCG and the complex also includes XCCR3. The ubiquitinated form specifically interacts with MTMR15/FAN1 (via UBZ-type zinc finger), leading to recruit MTMR15/FAN1 to sites of DNA damage. Interacts with DCLRE1B/Apollo. Highly expressed in germinal center cells of the spleen, tonsil, and reactive lymph nodes, and in the proliferating basal layer of squamous epithelium of tonsil, esophagus, oropharynx, larynx and cervix. Expressed in cytotrophoblastic cells of the placenta and exocrine cells of the pancreas. Highly expressed in testis, where expression is restricted to maturing spermatocytes. 4 isoforms of the human protein are produced by alternative splicing. Protein type: DNA repair, damage. Chromosomal Location of Human Ortholog: 3p26. Cellular Component: nucleoplasm; Golgi apparatus; intracellular membrane-bound organelle; condensed chromosome. Molecular Function: protein binding. Biological Process: gamete generation; synapsis; response to gamma radiation; DNA repair. Disease: Tracheoesophageal Fistula With Or Without Esophageal Atresia; Fanconi Anemia, Complementation Group D2

size1 :

48-Strip-Wells

price1 :

470 USD

size2 :

96-Strip-Wells

price2 :

680

size3 :

5x96-Strip-Wells

price3 :

3100

size4 :

10x96-Strip-Wells

price4 :

6095

more info or order :

MyBioSource product webpage