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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, Mouse, Rat
Application EIA, IF, WB
Validations
  • (2)
Cat. No. ABIN1450135
Quantity 0.1 mg
Datasheet Datasheet
Reactivity Human
Application ELISA, IHC
Validations
  • (1)
Cat. No. ABIN7166354
Quantity 100 μg
Datasheet Datasheet
Reactivity Human
Application ELISA
Validations
Cat. No. ABIN7166355
Quantity 100 μg
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 Insect Cells
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, Ppil2

Protein 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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