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Anti-Integrin Alpha 4 Antibody

SKU Product Brand Unit Availability Price Quantity  
AB-06-2468
Anti-Integrin Alpha 4 Antibody
Erpan Tech In stock

Specifications        

Product Cat#: AB-06-2468
Product type: Primary antibody
Antigen: Integrin alpha 4
Immunogen: Recombinant protein
Species immunized: Rabbit
Isotype: IgG
Applications: Western Blot (1:800-1:2000); Immunohistochemistry (1:80-1:200); Flow Cytometry (1:20-1:100)
Reactivity: Mouse, Rat and Human
Clonality (clone number): Monoclonal(JA09-36)
Buffer: Tris-HCl buffer (pH 7.4), 1% BSA, 40% glycerol, 0.05% NaN3.
Concentration: 1 mg/ml
Purity: Protein A affinity purified
Storage: Aliquot and freeze at -20℃. Avoid multiple freeze/thaw cycles.
Alternative names: 269C wild type antibody
Antigen CD49D, alpha 4 subunit of VLA 4 receptor antibody
CD49 antigen like family member D antibody
CD49 antigen-like family member D antibody
CD49d antibody
IA4 antibody
Integrin alpha 4 antibody
Integrin alpha 4 subunit antibody
Integrin alpha IV antibody
Integrin alpha-4 antibody
Integrin alpha-IV antibody
Integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA 4 receptor) antibody
ITA4_HUMAN antibody
ITGA4 antibody
MGC90518 antibody
OTTHUMP00000205320 antibody
Very late activation protein 4 receptor, alpha 4 subunit antibody
VLA 4 subunit alpha antibody
VLA-4 subunit alpha antibody
VLA4 antibody
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Target information

Plays an important role in chaperone-mediated autophagy, a process that mediates lysosomal degradation of proteins in response to various stresses and as part of the normal turnover of proteins with a long biological half-live (PubMed:8662539, PubMed:11082038, PubMed:18644871, PubMed:24880125, PubMed:27628032). Functions by binding target proteins, such as GAPDH and MLLT11, and targeting them for lysosomal degradation (PubMed:8662539, PubMed:11082038, PubMed:18644871, PubMed:24880125). Plays a role in lysosomal protein degradation in response to starvation (By similarity). Required for the fusion of autophagosomes with lysosomes during autophagy (PubMed:27628032). Cells that lack LAMP2 express normal levels of VAMP8, but fail to accumulate STX17 on autophagosomes, which is the most likely explanation for the lack of fusion between autophagosomes and lysosomes (PubMed:27628032). Required for normal degradation of the contents of autophagosomes (PubMed:27628032). Required for efficient MHCII-mediated presentation of exogenous antigens via its function in lysosomal protein degradation; antigenic peptides generated by proteases in the endosomal/lysosomal compartment are captured by nascent MHCII subunits (PubMed:20518820). Is not required for efficient MHCII-mediated presentation of endogenous antigens (PubMed:20518820).

Provider

Erpantech Laboratory

download

MSDS-AB-06-2468.pdf (114 downloads)