WFS1 (NM_006005) Human Mass Spec Standard
CAT#: PH302901
WFS1 MS Standard C13 and N15-labeled recombinant protein (NP_005996)
View other "WFS1" proteins (7)
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CNY 14,250.00
Specifications
Product Data | |
Description | WFS1 MS Standard C13 and N15-labeled recombinant protein (NP_005996) |
Species | Human |
Expression Host | HEK293 |
Expression cDNA Clone or AA Sequence | RC202901 |
Predicted MW | 100.3 kDa |
Protein Sequence |
>RC202901 protein sequence
Red=Cloning site Green=Tags(s) MDSNTAPLGPSCPQPPPAPQPQARSRLNATASLEQERSERPRAPGPQAGPGPGVRDAAAPAEPQAQHTRS RERADGTGPTKGDMEIPFEEVLERAKAGDPKAQTEVGKHYLQLAGDTDEELNSCTAVDWLVLAAKQGRRE AVKLLRRCLADRRGITSENEREVRQLSSETDLERAVRKAALVMYWKLNPKKKKQVAVAELLENVGQVNEH DGGAQPGPVPKSLQKQRRMLERLVSSESKNYIALDDFVEITKKYAKGVIPSSLFLQDDEDDDELAGKSPE DLPLRLKVVKYPLHAIMEIKEYLIDMASRAGMHWLSTIIPTHHINALIFFFIVSNLTIDFFAFFIPLVIF YLSFISMVICTLKVFQDSKAWENFRTLTDLLLRFEPNLDVEQAEVNFGWNHLEPYAHFLLSVFFVIFSFP IASKDCIPCSELAVITGFFTVTSYLSLSTHAEPYTRRALATEVTAGLLSLLPSMPLNWPYLKVLGQTFIT VPVGHLVVLNVSVPCLLYVYLLYLFFRMAQLRNFKGTYCYLVPYLVCFMWCELSVVILLESTGLGLLRAS IGYFLFLFALPILVAGLALVGVLQFARWFTSLELTKIAVTVAVCSVPLLLRWWTKASFSVVGMVKSLTRS SMVKLILVWLTAIVLFCWFYVYRSEGMKVYNSTLTWQQYGALCGPRAWKETNMARTQILCSHLEGHRVTW TGRFKYVRVTDIDNSAESAINMLPFFIGDWMRCLYGEAYPACSPGNTSTAEEELCRLKLLAKHPCHIKKF DRYKFEITVGMPFSSGADGSRSREEDDVTKDIVLRASSEFKSVLLSLRQGSLIEFSTILEGRLGSKWPVF ELKAISCLNCMAQLSPTRRHVKIEHDWRSTVHGAVKFAFDFFFFPFLSAA TRTRPLEQKLISEEDLAANDILDYKDDDDKV |
Tag | C-Myc/DDK |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Concentration | >0.05 µg/µL as determined by microplate BCA method |
Labeling Method | Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine |
Buffer | 25 mM Tris-HCl, 100 mM glycine, pH 7.3 |
Reference Data | |
RefSeq | NP_005996 |
RefSeq Size | 3640 |
RefSeq ORF | 2670 |
Synonyms | CTRCT41; WFRS; WFS; WFSL |
Locus ID | 7466 |
Cytogenetics | 4p16.1 |
Summary | This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009] |
Protein Families | Druggable Genome, Transmembrane |
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Other Versions
SKU | Description | Size | Price |
---|---|---|---|
LC416929 | WFS1 HEK293T cell transient overexpression lysate (as WB positive control) |
CNY 900.00 |
|
LC429034 | WFS1 HEK293T cell transient overexpression lysate (as WB positive control) |
CNY 1,470.00 |
|
LY416929 | Transient overexpression lysate of Wolfram syndrome 1 (wolframin) (WFS1), transcript variant 1 |
CNY 3,080.00 |
|
LY429034 | Transient overexpression lysate of Wolfram syndrome 1 (wolframin) (WFS1), transcript variant 2 |
CNY 4,840.00 |
|
PH327925 | WFS1 MS Standard C13 and N15-labeled recombinant protein (NP_001139325) |
CNY 14,250.00 |
|
TP302901 | Purified recombinant protein of Homo sapiens Wolfram syndrome 1 (wolframin) (WFS1), transcript variant 1, 20 µg |
CNY 2,900.00 |
|
TP327925 | Purified recombinant protein of Homo sapiens Wolfram syndrome 1 (wolframin) (WFS1), transcript variant 2, 20 µg |
CNY 2,900.00 |