Product Name	FAM70A
Chinese Name	FAM70A蛋白抗体
Alias	family with sequence similarity 70, member A; FLJ20716; hypothetical protein T255A_HUMAN.
literatures	Specific References  (1)     |     SL11006R has been referenced in 1 publications. [IF=5.753] Zhang NN et al. Fam70A binds Wnt5a to regulate meiosis and quality of Mouseoocytes. Cell Prolif. 2020 Jun;53(6):e12825.  WB IHC IF IP ;  Mouse.   PubMed:32391621
Research Area	Cell biology  Developmental biology  Chromatin and nuclear signals
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	(predicted: Human, Mouse, Dog, Horse, Rabbit, 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	38kDa
Cellular localization	The cell membrane
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human FAM70A: 1-100/394
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 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. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. 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. The FAM70A gene product has been provisionally designated FAM70A pending further characterization. Subcellular Location: Membrane; Multi-pass membrane protein Similarity: Belongs to the TMEM255 family. SWISS: Q5JRV8 Gene ID: 55026 Database links: Entrez Gene: 55026 Human Entrez Gene: 245386 Mouse Entrez Gene: 313453 Rat SwissProt: Q9BE63 Cynomolgus monkey SwissProt: Q5JRV8 Human SwissProt: Q8BHW5 Mouse SwissProt: Q7TMP6 Rat Unigene: 437563 Human Unigene: 72979 Mouse Unigene: 163441 Rat

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