• Featured Product
  • KD/KO Validated

SPATA7 Polyclonal antibody

SPATA7 Polyclonal Antibody for WB, IP, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IP, IF, IHC, ELISA

Conjugate

Unconjugated

Cat no : 12020-1-AP

Synonyms

HSD 3.1, HSD3, SPATA7, spermatogenesis associated 7


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Tested Applications

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

Recommended dilution

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.

Product Information

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

Tested Reactivity human, mouse, rat
Cited Reactivitymouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen SPATA7 fusion protein Ag2649 相同性解析による交差性が予測される生物種
Full Name 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
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.

Background Information

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.

Protocols

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

Publications

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