Neon drop · Free ship $75+ · Enter the grid
Signal · Product Feed

AASS Polyclonal Antibody, 50ul DNA Fragments |disease:A chromosomal aberration involving NFKB2

SKU: 13838074737

4.7
USD142.00 USD163.00

Pay in 4 interest-free payments of $35.50 Learn more

Shipping Estimate
USA
  • USA
  • CAN

Ships within 48 hours · Estimated delivery Aug 26 - Aug 31

Live Spec

AASS Polyclonal Antibody, 50ul DNA Fragments |disease:A chromosomal aberration involving NFKB2AASS encodes a bifunctional enzyme (aminoadipate semialdehyde synthase) that catalyzes the first two steps in the mammalian lysine degradation pathway. The N terminal and the C terminal portions of this enzyme contain lysine ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha aminoadipic semialdehyde. Mutations in AASS are associated with familial hyperlysinemia.

Store: happygoluckyhtx.com · Domain: happygoluckyhtx.com

Description

|disease:A chromosomal aberration involving NFKB2 is found in a cutaneous T-cell leukemia (C-TCL) cell line

The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent

SODs are antioxidant enzymes that catalyze the conversion of superoxide radicals into hydrogen peroxide and oxygen| which may protect the brain| lungs| and other tissues from oxidative stress

SEMA3F (semaphorin 3F) encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development

the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs

AASS Polyclonal Antibody, 50ul DNA Fragments |disease:A chromosomal aberration involving NFKB2AASS encodes a bifunctional enzyme (aminoadipate semialdehyde synthase) that catalyzes the first two steps in the mammalian lysine degradation pathway. The N terminal and the C terminal portions of this enzyme contain lysine ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha aminoadipic semialdehyde. Mutations in AASS are associated with familial hyperlysinemia.

Exchange/Return Notes
  • We offer a 30-day return/exchange service after receiving.
  • Final sale items are not eligible for returns or exchanges.
  • To process your return/exchange, please contact us at [email protected]
  • Please click here for more details>>> Return & Exchange Policy

You may also like

recommand products