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Alternative Name: CPXM1
an autosomal disease characterized by a variable group of congenital anomalies that include complex cardiac malformations such as conotruncal heart malformations that may lead to cardiac outflow tract defects
Immunogen: Recombinant fusion protein of human ISY1(NP_001186398
Background: This gene encodes a member of the scavenger receptor cysteine-rich (SRCR) superfamily
AA Sequence: SPL PITPVNATCA IRHPCHNNLM NQIRSQLAQL NGSANALFIL YYTAQGEPFP NNLDKLCGPN VTDFPPFHAN GTEKAKLVEL YRIVVYLGTS LGNITRDQKI LNPSALSLHS KLNATADILR GLLSNVLCRL CSKYHVGHVD VTYGPDTSGK DVFQKKKLGC QLLGKYKQII AVLAQAF
NMDAR2A Polyclonal Antibody-BS70491 Size:50µl Alternative Name: CPXM1NMDAR2A Polyclonal Antibody Sizes: 50l, 100l Catalogue Numbers: BS70491 50, BS70491 100 Product: 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Swiss Prot: Q12879 Host: Rabbit Reactivity: Mouse, Rat Applications: WB, IF ICC All Applications: WB,1: 500 1: 1000 IF ICC,1: 50 1: 200 Background: This gene encodes a member of the glutamate gated ion channel protein family. The encoded protein is an N methyl D aspartate (NMDA) receptor subunit.
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