Product Name	C3ORF31
Chinese Name	3号染色体开放阅读框31抗体
Alias	C3orf31; Chromosome 3 open reading frame 31; MGC16471; MMP37 like protein; MMP37 like protein mitochondrial; MMP37-like protein, mitochondrial; MMP37_HUMAN.
Research Area	Tumour  Cell biology  immunology
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	(predicted: Human, Mouse, Rat, Dog, Pig, Cow, Sheep, )
Applications	WB=1:500-2000 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	33kDa
Cellular localization	cytoplasmic The cell membrane
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human C3ORF31 : 101-200/316
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	C3orf31 (chromosome 3 open reading frame 31), also known as MGC16471 or DKFZp434E0519, is a 316 amino acid mitochondrial protein that belongs to the MMP37 family and may be involved in translocation of transit peptide-containing proteins across the mitochondrial inner membrane. C3orf24 is encoded by a gene that maps to human chromosome 3p25.2. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3. Function: May be involved in the translocation of transit peptide-containing proteins across the mitochondrial inner membrane (By similarity). Subcellular Location: Mitochondrion (By similarity). Similarity: Belongs to the MMP37/TAM41 family. SWISS: Q96BW9 Gene ID: 132001 Database links: Entrez Gene: 514330 Cow Entrez Gene: 100725702 Guinea pig Entrez Gene: 100051402 Horse Entrez Gene: 132001 Human Entrez Gene: 362419 Rat Entrez Gene: 641323 Zebrafish Omim: 614948 Human SwissProt: Q32L81 Cow SwissProt: Q96BW9 Human SwissProt: Q3TUH1 Mouse SwissProt: Q3B7H2 Zebrafish

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