FAM161A 产品
(Family with Sequence Similarity 161, Member A (FAM161A))
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This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011].
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FAM161A 抗体
High quality antibodies with extensive validation data.
FAM161A 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended FAM161A 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, ELISA, IHC
Validations
- (3)
Cat. No.
ABIN7165430
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Dog, Human, Mouse, Pig, Rabbit
Application
WB
Validations
- (1)
Cat. No.
ABIN6747442
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Dog, Guinea Pig, Horse, Human, Monkey, Rabbit
Application
WB
Validations
- (1)
Cat. No.
ABIN6747443
Quantity
100 μL
Datasheet
Datasheet
Recommended FAM161A 蛋白
Synonyms and alternative names related to FAM161A
family with sequence similarity 161 member A (FAM161A), family with sequence similarity 161, member A (Fam161a), family with sequence similarity 161, member A (FAM161A), 4930430E16Rik, RGD1304999, RP28Protein level used designations for FAM161A
- protein FAM161A
- retinitis pigmentosa 28 (autosomal recessive)
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