Recombinant Human UBE1/UBA1 Protein (His & GST Tag)

Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Dry Ice Shipment: No

Product Documents

MSDS

Alternative Products

Cat	Name
MBS517738-03	UBA1 (UBE1), Active
MBS515704-01	UBA1 (UBE1) Protein
MBS515704-03	UBA1 (UBE1) Protein
MBS517738-02	UBA1 (UBE1), Active
MBS515704-02	UBA1 (UBE1) Protein
MBS517738-01	UBA1 (UBE1), Active
GWB-ACB42F	UBE1 (UBA1), Active Human Recombinant Protein
80301-1	UBE1 (UBA1), FLAG-tag
80301-2	UBE1 (UBA1), FLAG-tag
UB1-H5248-100ug	Human UBE1 / UBA1 Protein, His Tag

Recombinant Human UBE1/UBA1 Protein (His & GST Tag)

CAT:

763-PKSH030942

Size:

50 µg

Price:

Ask

For price, please contact [email protected].

Recombinant Human UBE1/UBA1 Protein (His & GST Tag)

Background: UBE1, also known as UBA1, belongs to the ubiquitin-activating E1 family. UBE1 gene complements an X-linked mouse temperature-sensitive defect in DNA synthesis, and thus may function in DNA repair. It is part of a gene cluster on chromosome Xp11.23. UBE1 catalyzes the first step in ubiquitin conjugation to mark cellular proteins for degradation. It also catalyzes the first step in ubiquitin conjugation to mark cellular proteins for degradation by first adenylating its C-terminal glycine residue with ATP, and thereafter linking this residue to the side chain of a cysteine residue in E1, yielding an ubiquitin-E1 thioester and free AMP. Defects in UBA1 can cause spinal muscular atrophy X-linked type 2 (SMAX2), also known as X-linked lethal infantile spinal muscular atrophy, distal X-linked arthrogryposis multiplex congenita or X-linked arthrogryposis type 1 (AMCX1). Spinal muscular atrophy refers to a group of neuromuscular disorders characterized by degeneration of the anterior horn cells of the spinal cord, leading to symmetrical muscle weakness and atrophy. SMAX2 is a lethal infantile form presenting with hypotonia, areflexia, and multiple congenital contractures.
Synonyms: A1S9, A1S9T, A1ST, AMCX1, CFAP124, CTD-2522E6.1, GXP1, POC20, SMAX2, UBA1A, UBE1, UBE1X
UniProt: P22314
Accession Number: NP_003325.2
Host: Baculovirus
Origin Species: Human
Tag: N-His-GST
Sequence: Ser 2-Arg 1058
Field of Research: Cell biology;epigenetics and nuclear signal
Purity: > 96 % as determined by reducing SDS-PAGE.
Bioactivity: Not validated for activity
Reconstitution: Please refer to the printed manual for detailed information.
Molecular Weight: 130 kDa
Shipping Conditions: This product is provided as lyophilized powder which is shipped with ice packs.
Storage Conditions: Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.

Complementary Product Range

Our range of products, including Recombinant Human UBE1/UBA1 Protein (His & GST Tag), falls within the same field of application and can be used across various research projects. These products are carefully selected for their high performance and reliability, supporting the diverse needs of modern laboratories. Whether for ongoing studies or future experiments, they are designed to help researchers achieve their scientific goals. Here are some related products that may be of interest for similar or future applications:

Each item in our collection, is tested for precision and quality, ensuring dependable solutions for your research. As we continue to incorporate the latest advancements, Gentaur ensures that our product range remains relevant and versatile, providing you with the tools needed for both current and future projects.

Find us on

Cat	Name
PKSH030942	Recombinant Human UBE1/UBA1 Protein (His & GST Tag)
E-AB-17501-01	UBA1 Polyclonal Antibody
E-AB-17501-02	UBA1 Polyclonal Antibody
E-AB-17502-04	UBA1 Polyclonal Antibody
E-AB-17502-02	UBA1 Polyclonal Antibody
E-AB-63690-03	UBA1 Polyclonal Antibody
E-AB-63690-01	UBA1 Polyclonal Antibody
E-AB-17502-03	UBA1 Polyclonal Antibody
E-AB-17502-01	UBA1 Polyclonal Antibody
E-AB-63690-02	UBA1 Polyclonal Antibody