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Key Documents

GW22845

Sigma-Aldrich

Anti-SSR4 antibody produced in chicken

affinity isolated antibody, buffered aqueous solution

Synonym(s):

Anti-Signal sequence receptor, δ

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

biological source

chicken

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

mouse, rat, human

manufacturer/tradename

Genway 15-288-22845

technique(s)

western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... SSR4(6748)

Immunogen

Immunogen Sequence: GI # 5454090, sequence 61-130
Recombinant signal sequence receptor, delta

Application

Anti-SSR4 antibody produced in chicken is suitable for western blotting analysis at a dilution of 1:500, for tissue or cell staining at a dilution of 1:200.

Biochem/physiol Actions

Translocon-associated heterotetrameric protein subunit δ is a protein encoded by the SSR4 gene in humans. It is found to be upregulated in tumors of advanced stages. It acts as a candidate gene with potential functions that might be associated with ultraviolet-induced melanomagenesis and metastasis. Mutation in SSR4 gene causes congenital disorders of glycosylation (CDG).

Physical form

Solution in phosphate buffered saline containing 0.02% sodium azide.

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Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Zhiqiang Wang et al.
Melanoma research, 14(2), 107-114 (2004-04-02)
The human ortholog of Monodelphis translocon-associated protein delta subunit gene (TRAPD) was identified as a differentially expressed transcript using the differential display technique, and the two phenotypically distinct opossum melanoma cell lines TD6b and TD15L2 as the tissue resource. The
Marie Estelle Losfeld et al.
Human molecular genetics, 23(6), 1602-1605 (2013-11-13)
Nearly 50 congenital disorders of glycosylation (CDG) are known, but many patients biochemically diagnosed with CDG do not have mutations in known genes. Here, we describe a 16-year-old male who was born with microcephaly, developed intellectual disability, gastroesophageal reflux and

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