SPG21 Polyclonal antibody, PBS Only

SPG21 Polyclonal Antibody for WB, Indirect ELISA
Cat No. 19815-1-PBS

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, Indirect ELISA

ABHD21, Acid cluster protein 33, ACP33, BM 019, GL010

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -


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保証・サポートについて

テクニカルサポートまたはご購入後1年間の交換/補填対応を承ります。詳細はこちらをご覧ください。


Tested Applications

Recommended dilution

ApplicationDilution
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Product Information

19815-1-PBS targets SPG21 in WB, Indirect ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag13851

Product name: Recombinant human SPG21 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 1-308 aa of BC000244

Sequence: MGEIKVSPDYNWFRGTVPLKKIIVDDDDSKIWSLYDAGPRSIRCPLIFLPPVSGTADVFFRQILALTGWGYRVIALQYPVYWDHLEFCDGFRKLLDHLQLDKVHLFGASLGGFLAQKFAEYTHKSPRVHSLILCNSFSDTSIFNQTWTANSFWLMPAFMLKKIVLGNFSSGPVDPMMADAIDFMVDRLESLGQSELASRLTLNCQNSYVEPHKIRDIPVTIMDVFDQSALSTEAKEEMYKLYPNARRAHLKTGGNFPYLCRSAEVNLYVQIHLLQFHGTKYAAIDPSMVSAEELEVQKGSLGISQEEQ

相同性解析による交差性が予測される生物種
Full Name spastic paraplegia 21 (autosomal recessive, Mast syndrome)
Calculated molecular weight 308 aa, 35 kDa
Observed molecular weight35 kDa
GenBank accession numberBC000244
Gene Symbol SPG21
Gene ID (NCBI) 51324
Conjugate Unconjugated
Form
FormLiquid
Purification MethodAntigen affinity purification
UNIPROT IDQ9NZD8
Storage Buffer PBS only{{ptg:BufferTemp}}7.3
Storage ConditionsStore at -80°C.

Background Information

SPG21, also known as Maspardin, is a protein encoded by the SPG21 gene on human chromosome 15q22.31. SPG21 is critical for the proper movement and positioning of lysosomes within neurons, which is essential for maintaining axonal health. Mutations in the SPG21 gene underlie hereditary spastic paraplegia (SPG) type 21 (also known as Mast syndrome). This is a complex form of SPG characterized by motor coordination defects due to axonal degeneration of corticospinal neurons and associated with dementia, cerebellar, and extrapyramidal abnormalities and, in some cases, seizures.(PMID: 41400694,PMID: 34492745)

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