Product Name	APOL5
Chinese Name	载LipoproteinL5抗体
Alias	APOL 5; APOL V; APOL5; Apolipoprotein L5; Apolipoprotein L; Apolipoprotein L V; apoL-V; Apolipoprotein L 5; APOLV; OTTHUMP00000028773; APOL5_HUMAN.
Research Area	Tumour  Cardiovascular  Cell biology  The new supersedes the old
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	(predicted: Human, )
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	47kDa
Cellular localization	cytoplasmic
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human APOL5/Apolipoprotein L5: 301-400/433
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	The apolipoprotein L gene family maps to a region on chromosome 22 and encodes six highly homologous proteins designated apoL-I, apoL-II, apoL-III, apoL-IV, apoL-V and apoL-VI, all of which function as components of plasma lipoproteins. ApoL-V (apolipoprotein L-V), also known as APOL5, is a 433 amino acid protein that localizes to the cytoplasm and belongs to the apolipoprotein L family. Expressed in a variety of tissues including testis, stomach, uterus and skeletal muscle, apoL-V is thought to affect the movement of lipids in the cytoplasm and may allow the binding of lipids to organelles. Like other members of the apolipoprotein L family, apoL-V is thought to be involved in the development of schizophrenia. Function: Apolipoprotein L 5 is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. Subcellular Location: Cytoplasm (Probable). Tissue Specificity: Low level of expression; detected in uterus, testis, skeletal muscle and stomach. Similarity: Belongs to the apolipoprotein L family. SWISS: Q9BWW9 Gene ID: 80831 Database links: Entrez Gene: 80831 Human Omim: 607255 Human SwissProt: Q9BWW9 Human

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