YPEL1 Products
(Yippee-Like 1 (YPEL1))
Categories
This gene encodes a potential zinc-binding protein and is located in the region associated with DiGeorge syndrome on chromosome 22. The encoded protein may play a role in the regulation of cellular morphology and may function during craniofacial development. [provided by RefSeq, Jul 2008].
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Featured YPEL1 Categories
YPEL1 Antibodies
High quality antibodies with extensive validation data.
YPEL1 Proteins
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended YPEL1 Antibodies
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, IHC, IHC (p)
Validations
- (2)
Cat. No.
ABIN1804163
Quantity
50 μg
Datasheet
Datasheet
Reactivity
Human
Application
ELISA, IHC
Validations
- (1)
Cat. No.
ABIN7166354
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human, Mouse, Rat
Application
WB, IF, EIA
Validations
- (2)
Cat. No.
ABIN1450135
Quantity
0.1 mg
Datasheet
Datasheet
Recommended YPEL1 ELISA Kits
Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Analytical Method
Quantitative Sandwich ELISA
Validations
Cat. No.
ABIN6234297
Quantity
96 tests
Datasheet
Datasheet
Recommended YPEL1 Proteins
Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Source
Tobacco (Nicotiana tabacum)
Validations
- (1)
Cat. No.
ABIN3075682
Quantity
1 mg
Datasheet
Datasheet
Reactivity
Human
Source
Escherichia coli (E. coli)
Validations
- (1)
Cat. No.
ABIN5710638
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human
Source
HEK-293 Cells
Validations
- (1)
Cat. No.
ABIN2735729
Quantity
20 μg
Datasheet
Datasheet
Synonyms and alternative names related to YPEL1
yippee like 1 (YPEL1), yippee-like 1 (Drosophila) (Ypel1), yippee-like 1 (Ypel1), 0610009L05Rik, 1700016N17Rik, 1700019O22Rik, 4921520K19Rik, 4930511F14Rik, AV118478, Dgl1, mdgl-1, Ppil2Protein level used designations for YPEL1
- DiGeorge syndrome-related protein
- protein yippee-like 1
- DGL-1
- cardiac Abnormality/abnormal facies (CATCH22), microdeletion syndrome
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