Thermo Fisher Scientific NMDAR2B Monoclonal Antibody (B3-13B11)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
320700 | - | Thermo Fisher Scientific 320700 NMDAR2B Monoclonal Antibody (B3-13B11) 100 ug pk | 재고문의 | pk | 636,000원 | - | 699,600원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1-5 µg/mL
View 2 publications 2 publications
Immunohistochemistry (Frozen) (IHC (F))
5-10 µg/mL
Immunocytochemistry (ICC/IF)
-
View 1 publication 1 publication
ELISA (ELISA)
1.0-5 µg/mL
Immunoprecipitation (IP)
-
View 1 publication 1 publication
Product Specifications
Species Reactivity
Dog, Human, Mouse, Non-human primate, Rat
Published species
Human, Rat
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
B3-13B11
Immunogen
NMDA receptor 2B fusion protein
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.5 mg/mL
Purification
Protein A
Storage buffer
PBS, pH 7.4
Contains
0.1% sodium azide
Storage conditions
-20°C
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2533061
Target Information
NMDAR2B is a member of the N-methyl-D-aspartate (NMDA) class of ionotropic glutamate receptors. NMDA receptors (NMDAR) have been shown to be involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. NMDAR play a role in neuronal development and has been implicated in several disorders of the central nervous system including Alzheimer`s Disease, epilepsy and ischemic neuronal cell death. Overexpression of the NR2B subunit of the receptor has been associated with increases in learning and memory while aged, memory impaired animals have deficiencies in NR2B expression. Tyr1472 on NR2B is phosphorylated and this may lead to the increased expression of the NMDAR at the synapse that plays a role in synaptic plasticity. NMDR2B is a heterotrimer comprised of seven enetically encoded and differentially expressed subunits that include NR1, NR2 and NR3. Diseases associated with the dysfunction of NMDAR2B include epileptic encephalopathy, autosomal dominant 6-related mental retardation.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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