DDHD2 polyclonal, anti-human, mouse
€295.00
In stock
SKU
K106958P
Catalog Number: K106958P
Size: 100 μl
Other size: 50 μl
Isotype: RabbitIgG
Applications: WB, IHC
Request Manual
Questions? Contact us!
Size: 100 μl
Other size: 50 μl
Isotype: RabbitIgG
Applications: WB, IHC
Request Manual
Questions? Contact us!
Background:
This gene encodes a phospholipase enzyme containing sterile-alpha-motif (SAM), WWE, and DDHD domains. This protein participates in membrane trafficking between the endoplastic reticulum and the Golgi body. Mutations in this gene can cause autosomal recessive spastic paraplegia 54. Alternative splicing results in multiple transcript variants
Synonyms: DDHD domain containing 2, DDHD2, KIAA0725, KIAA0725p, Phospholipase DDHD2, SAMWD1
Cellular Location: Cytoplasm
Immunogen:
Recombinant protein of human DDHD2
Gene Symbol: DDHD2
Gene ID: 23259
Swiss prot: O94830
Calculated MW: 81kDa
Recommended dilution:
WB 1:8000-12000, IHC 1:100-300
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
This gene encodes a phospholipase enzyme containing sterile-alpha-motif (SAM), WWE, and DDHD domains. This protein participates in membrane trafficking between the endoplastic reticulum and the Golgi body. Mutations in this gene can cause autosomal recessive spastic paraplegia 54. Alternative splicing results in multiple transcript variants
Synonyms: DDHD domain containing 2, DDHD2, KIAA0725, KIAA0725p, Phospholipase DDHD2, SAMWD1
Cellular Location: Cytoplasm
Immunogen:
Recombinant protein of human DDHD2
Gene Symbol: DDHD2
Gene ID: 23259
Swiss prot: O94830
Calculated MW: 81kDa
Recommended dilution:
WB 1:8000-12000, IHC 1:100-300
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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