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Product Name FUNDC2 Chinese Name Cervical cancer oncogene 3/宫颈癌原癌基因3抗体 Alias Cervical cancer oncogene 3; Cervical cancer proto oncogene 3 protein; DC44; FLJ33773; FUN14 domain containing 2; FUN14 domain containing protein 2; FUNDC 2; HCBP 6; HCBP6; FUND2_HUMAN; HCC 3; HCC3; Hepatitis C virus core binding protein 6; MGC131676; MGC2495; OTTHUMP00000015441; OTTHUMP00000061459; PD03104. Research Area Tumour Cell biology transcriptional regulatory factor Bacteria and viruses The new supersedes the old Mitochondrion Epigenetics Immunogen Species Rabbit Clonality Polyclonal React Species (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, ) Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 21kDa Cellular localization The nucleus cytoplasmic Mitochondrion Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human FUNDC2: 101-189/189 Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail FUNDC2 is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Function:
The function of FUNDC2 (FUN14 domain-containing protein 2) is unknown.
Subcellular Location:
Mitochondrial
Similarity:
Belongs to the FUN14 family.
SWISS:
Q9BWH2
Gene ID:
65991
Database links:Entrez Gene: 65991 Human
Entrez Gene: 67391 Mouse
SwissProt: Q9BWH2 Human
SwissProt: Q9D6K8 Mouse
Unigene: 356050 Human
Unigene: 126404 Mouse
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