LAB (Phospho-Tyr136) rabbit pAb
Product Specifications
Background
Linker for activation of T-cells family member 2 (LAT2) Homo sapiens This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]
Product Name Alternative
Linker for activation of T-cells family member 2 (Linker for activation of B-cells) (Membrane-associated adapter molecule) (Non-T-cell activation linker) (Williams-Beuren syndrome chromosomal region 15 protein) (Williams-Beuren syndrome chromosomal region 5 protein)
Gene ID
7462
Swiss Prot
Q9GZY6
Cross Reactivity
Human; Mouse; Rat
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Dilution
WB 1:500-2000
Buffer
Liquid in PBS containing 50% glycerol, and 0.146% sodium azide.
Molecular Weight
30
Storage Conditions
-20°C/1 year
Protein Weight
30
Available Sizes
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