TRAPPC9 Antibody (PACO12896)
제품 코드를 사용하여 Assay Genie 메인 사이트를 통해 주문합니다.
주문- SKU:
- PACO12896
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Application:
- IHC
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
Antibody Name: | TRAPPC9 Antibody (PACO12896) |
Antibody SKU: | PACO12896 |
Size: | 50ul |
Host Species: | Rabbit |
Tested Applications: | ELISA, WB, IHC |
Recommended Dilutions: | |
Species Reactivity: | Human, Mouse, Rat |
Immunogen: | Human TRAPPC9 |
Form: | Liquid |
Storage Buffer: | PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles. |
Purification Method: | Antigen Affinity purified |
Clonality: | Polyclonal |
Isotype: | IgG |
Conjugate: | Non-conjugated |
Synonyms: | trafficking protein particle complex 9;TRAPPC9;IBP;IKBKBBP;KIAA1882;MGC4737;MGC4769;NIBP;T1;TRS120 ; |
UniProt Protein Function: | NIBP: Functions as an activator of NF-kappa-B through increased phosphorylation of the IKK complex. May function in neuronal cells differentiation. May play a role in vesicular transport from endoplasmic reticulum to Golgi. Defects in TRAPPC9 are the cause of mental retardation autosomal recessive type 13 (MRT13). Mental retardation is characterized by significantly below average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Brain magnetic resonance imaging of MRT13 patients indicates the presence of mild cerebral white matter hypoplasia. Microcephaly is present in some but not all affected individuals. Belongs to the NIBP family. 3 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Activator Chromosomal Location of Human Ortholog: 8q24.3 Cellular Component: Golgi apparatus; endoplasmic reticulum Biological Process: cell differentiation Disease: Mental Retardation, Autosomal Recessive 13 |
NCBI Summary: | This gene encodes a protein that likely plays a role in NF-kappa-B signaling. Mutations in this gene have been associated with autosomal-recessive cognitive disability. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010] |
UniProt Code: | Q96Q05 |
NCBI GenInfo Identifier: | 190359999 |
NCBI Gene ID: | 83696 |
NCBI Accession: | Q96Q05.2 |
UniProt Related Accession: | Q96Q05 |
Molecular Weight: | 127kDa; 128kDa; 139kDa |
NCBI Full Name: | Trafficking protein particle complex subunit 9 |
NCBI Synonym Full Names: | trafficking protein particle complex 9 |
NCBI Official Symbol: | TRAPPC9 |
NCBI Official Synonym Symbols: | T1; IBP; NIBP; MRT13; TRS120; IKBKBBP |
NCBI Protein Information: | trafficking protein particle complex subunit 9 |
UniProt Protein Name: | Trafficking protein particle complex subunit 9 |
UniProt Synonym Protein Names: | NIK- and IKBKB-binding protein; Tularik gene 1 protein |
Protein Family: | Trafficking protein particle complex |
UniProt Gene Name: | TRAPPC9 |
UniProt Entry Name: | TPPC9_HUMAN |