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FLVC2 (C-Term), (AA 485-515) antibody

Details for Product No. ABIN952343
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Antigen
Epitope
C-Term, AA 485-515
(2), (2)
Reactivity
Human
(2)
Host
Rabbit
(2)
Clonality
Polyclonal
Application
ELISA, Western Blotting (WB)
(2)
Pubmed 4 references available
Quantity 0.4 mL
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Availability Will be delivered in 6 to 8 Business Days
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Catalog No. ABIN952343
357.50 $
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Immunogen KLH conjugated synthetic peptide between 485~515 amino acids from the C-terminal region of Human FLVC2. Genename: FLVCR2
Specificity This antibody recognizes Human FLVC2 (C-term).
Purification Affinity Chromatography on Protein A
Background The FLVCR2 gene encodes a transmembrane protein that belongs to the major facilitator superfamily of secondary carriers that transport small solutes in response to chemiosmotic ion gradients, such as calcium.
Alternate names: C14orf58, CCT, Calcium-chelate transporter, FLVCR2, Feline leukemia virus subgroup C receptor-related protein 2
Molecular Weight 57241 Da
Gene ID 55640
NCBI Accession NP_001182212
Restrictions For Research Use only
Format Liquid
Concentration 0.25 mg/mL
Buffer PBS containing 0.09% (w/v) Sodium Azide as preservative
Preservative Sodium azide
Precaution of Use This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice Avoid repeated freezing and thawing.
Storage 4 °C/-20 °C
Storage Comment Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
Expiry Date 12 months
Background publications Heilig, Eckenberg, Petit et al.: "The DNA sequence and analysis of human chromosome 14." in: Nature, Vol. 421, Issue 6923, pp. 601-7, 2003 (PubMed).

Brasier, Tikellis, Xuereb et al.: "Novel hexad repeats conserved in a putative transporter with restricted expression in cell types associated with growth, calcium exchange and homeostasis." in: Experimental cell research, Vol. 293, Issue 1, pp. 31-42, 2004 (PubMed).

Brown, Fung, Tailor: "Comprehensive mapping of receptor-functioning domains in feline leukemia virus subgroup C receptor FLVCR1." in: Journal of virology, Vol. 80, Issue 4, pp. 1742-51, 2006 (PubMed).

Meyer, Ricketts, Morgan et al.: "Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)." in: American journal of human genetics, Vol. 86, Issue 3, pp. 471-8, 2010 (PubMed).

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