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  • KD/KO Validated

SPATA7 Polyclonal antibody

SPATA7 Polyclonal Antibody for WB, IP, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IP, ELISA and More (2)

Conjugate

Unconjugated

Cat no : 12020-1-AP

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Synonyms

HSD 3.1, HSD3, SPATA7, spermatogenesis associated 7



经过测试的应用

Positive WB detected inPC-3 cells, mouse testis tissue, rat testis tissue
Positive IP detected inmouse testis tissue

推荐稀释比

ApplicationDilution
Western Blot (WB)WB : 1:500-1:1000
Immunoprecipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

12020-1-AP targets SPATA7 in WB, IP, IF, IHC, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Applications WB, IP, ELISA Application Description
Cited ApplicationsWB, IF, IHC
Tested Reactivity human, mouse, rat
Cited Reactivitymouse
Immunogen SPATA7 fusion protein Ag2649 种属同源性预测
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Full Name spermatogenesis associated 7
Synonyms HSD 3.1, HSD3, SPATA7, spermatogenesis associated 7
Calculated Molecular Weight 599 aa, 68 kDa
Observed Molecular Weight 68-80 kDa
GenBank Accession NumberBC008656
Gene Symbol SPATA7
Gene ID (NCBI) 55812
RRIDAB_2195380
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
UNIPROT IDQ9P0W8
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

SPATA7, also named as HSD3, may be involved in retinal function. It is interesting to note that mutations in SPATA7 cause LCA and RP/ARRP , two overlapping but distinct human retinal diseases. SPATA7 is another LCA and Juvenile RP Gene.(PMID:19268277) It is a highly conserved, vertebrate-specific protein which expressed in the mature retina. For some modification, the MW always migrate 5-8kd. The antibody can reoginze all the 3 isoforms of SPATA7.

实验方案

Product Specific Protocols
WB protocol for SPATA7 antibody 12020-1-APDownload protocol
IP protocol for SPATA7 antibody 12020-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
mouseIF, IHC

Am J Hum Genet

Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa.

Authors - Wang Hui H
mouseWB

Hum Mol Genet

Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina.

Authors - Aiden Eblimit
  • KO Validated
mouseWB,IF

Gene Ther

AAV8(Y733F)-mediated gene therapy in a Spata7 knockout mouse model of Leber congenital amaurosis and retinitis pigmentosa.

Authors - H Zhong
  • KO Validated
mouseWB

Exp Eye Res

Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice.

Authors - Aiden Eblimit